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Gene: LCA5L (lebercilin LCA5 like) Homo sapiens

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Symbol:

LCA5L

Name:

lebercilin LCA5 like

RGD ID:

1345568

HGNC Page

HGNC:1255

Description:

Predicted to be involved in intraciliary transport. Predicted to be active in axoneme.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C21orf13; hypothetical 76.5 kD protein, O95447, myosin heavy chain and kinesin homology; LCA5L, lebercilin like; Leber congenital amaurosis 5-like; leber congenital amaurosis 5-like protein; Lebercilin-like protein; MGC33295

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Lca5l (Leber congenital amaurosis 5-like)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Rattus norvegicus (Norway rat):	Lca5l (lebercilin LCA5 like)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Lca5l (lebercilin LCA5 like)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	LCA5L (lebercilin LCA5 like)	NCBI	Ortholog
Canis lupus familiaris (dog):	LCA5L (lebercilin LCA5 like)	HGNC	NCBI
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Lca5l (lebercilin LCA5 like)	NCBI	Ortholog
Sus scrofa (pig):	LCA5L (lebercilin LCA5 like)	HGNC	Ensembl, NCBI, OMA, OrthoDB, Panther
Chlorocebus sabaeus (green monkey):	LCA5L (lebercilin LCA5 like)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Lca5l (lebercilin LCA5 like)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Cggbp1 (CGG triplet repeat binding protein 1)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Lca5l (lebercilin LCA5 like)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Lca5l (Leber congenital amaurosis 5-like)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	CG6652	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|OrthoInspector\|PANTHER)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	21	39,405,728 - 39,445,805 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	21	40,777,654 - 40,817,704 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	21	39,699,640 - 39,737,998 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	21	39,699,639 - 39,737,998	NCBI
Celera	21	25,975,464 - 26,013,823 (-)	NCBI		Celera
Cytogenetic Map	21	q22.2	NCBI
HuRef	21	26,246,616 - 26,285,006 (-)	NCBI		HuRef
CHM1_1	21	40,338,935 - 40,377,266 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LCA5L	Human	autistic disorder		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Autism	ClinVar	PMID:21681106 and PMID:30208311

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LCA5L	Human	17beta-estradiol	decreases expression	ISO	Lca5l (Mus musculus)	6480464	Estradiol results in decreased expression of LCA5L mRNA	CTD	PMID:19484750
LCA5L	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	Lca5l (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in increased expression of LCA5L mRNA	CTD	PMID:33387578
LCA5L	Human	2,4-D	multiple interactions	ISO	Lca5l (Mus musculus)	6480464	[lard co-treated with Cholesterol more ...	CTD	PMID:37567420
LCA5L	Human	4,4'-sulfonyldiphenol	increases methylation	EXP		6480464	bisphenol S results in increased methylation of LCA5L gene	CTD	PMID:31601247
LCA5L	Human	4,4'-sulfonyldiphenol	affects methylation	ISO	Lca5l (Mus musculus)	6480464	bisphenol S affects the methylation of LCA5L gene	CTD	PMID:31683443
LCA5L	Human	4-hydroxyphenyl retinamide	increases expression	ISO	Lca5l (Mus musculus)	6480464	Fenretinide results in increased expression of LCA5L mRNA	CTD	PMID:28973697
LCA5L	Human	6-propyl-2-thiouracil	increases expression	ISO	Lca5l (Rattus norvegicus)	6480464	Propylthiouracil results in increased expression of LCA5L mRNA	CTD	PMID:24780913
LCA5L	Human	acrylamide	decreases expression	ISO	Lca5l (Rattus norvegicus)	6480464	Acrylamide results in decreased expression of LCA5L mRNA	CTD	PMID:28959563
LCA5L	Human	aldehydo-D-glucose	multiple interactions	ISO	Lca5l (Mus musculus)	6480464	[lard co-treated with Cholesterol more ...	CTD	PMID:37567420
LCA5L	Human	benzo[a]pyrene	increases expression	EXP		6480464	Benzo(a)pyrene results in increased expression of LCA5L mRNA	CTD	PMID:20064835 and PMID:22316170
LCA5L	Human	benzo[a]pyrene	affects methylation	EXP		6480464	Benzo(a)pyrene affects the methylation of LCA5L intron	CTD	PMID:30157460
LCA5L	Human	bis(2-ethylhexyl) phthalate	increases expression	ISO	Lca5l (Mus musculus)	6480464	Diethylhexyl Phthalate results in increased expression of LCA5L mRNA	CTD	PMID:34319233
LCA5L	Human	bisphenol A	decreases expression	ISO	Lca5l (Rattus norvegicus)	6480464	bisphenol A results in decreased expression of LCA5L mRNA	CTD	PMID:25181051 more ...
LCA5L	Human	bisphenol A	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in increased methylation of LCA5L gene	CTD	PMID:31601247
LCA5L	Human	copper atom	increases expression	ISO	Lca5l (Rattus norvegicus)	6480464	Copper deficiency results in increased expression of LCA5L mRNA	CTD	PMID:26033743
LCA5L	Human	copper(0)	increases expression	ISO	Lca5l (Rattus norvegicus)	6480464	Copper deficiency results in increased expression of LCA5L mRNA	CTD	PMID:26033743
LCA5L	Human	D-glucose	multiple interactions	ISO	Lca5l (Mus musculus)	6480464	[lard co-treated with Cholesterol more ...	CTD	PMID:37567420
LCA5L	Human	folic acid	decreases expression	ISO	Lca5l (Mus musculus)	6480464	Folic Acid results in decreased expression of LCA5L mRNA	CTD	PMID:25629700
LCA5L	Human	fructose	multiple interactions	ISO	Lca5l (Mus musculus)	6480464	[lard co-treated with Cholesterol more ...	CTD	PMID:37567420
LCA5L	Human	fulvestrant	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in increased methylation of LCA5L gene	CTD	PMID:31601247
LCA5L	Human	gentamycin	increases expression	ISO	Lca5l (Rattus norvegicus)	6480464	Gentamicins results in increased expression of LCA5L mRNA	CTD	PMID:33387578
LCA5L	Human	glucose	multiple interactions	ISO	Lca5l (Mus musculus)	6480464	[lard co-treated with Cholesterol more ...	CTD	PMID:37567420
LCA5L	Human	hexamethylene diisocyanate	increases methylation	EXP		6480464	1 and 6-hexamethylene diisocyanate results in increased methylation of LCA5L gene	CTD	PMID:25445006
LCA5L	Human	paracetamol	increases expression	EXP		6480464	Acetaminophen results in increased expression of LCA5L mRNA	CTD	PMID:29067470
LCA5L	Human	sodium arsenite	increases expression	EXP		6480464	sodium arsenite results in increased expression of LCA5L mRNA	CTD	PMID:38568856
LCA5L	Human	tetrachloromethane	decreases expression	ISO	Lca5l (Mus musculus)	6480464	Carbon Tetrachloride results in decreased expression of LCA5L mRNA	CTD	PMID:25270620
LCA5L	Human	tetraphene	increases expression	ISO	Lca5l (Mus musculus)	6480464	benz(a)anthracene results in increased expression of LCA5L mRNA	CTD	PMID:26377693
LCA5L	Human	titanium dioxide	decreases methylation	ISO	Lca5l (Mus musculus)	6480464	titanium dioxide results in decreased methylation of LCA5L gene and titanium dioxide results in decreased methylation of LCA5L promoter alternative form	CTD	PMID:35295148

Biological Process

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LCA5L	Human	intraciliary transport	involved_in	IBA	MGI:1923032 and PANTHER:PTN001047409	150520179		GO_Central	GO_REF:0000033

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LCA5L	Human	axoneme	is_active_in	IBA	FB:FBgn0036687 more ...	150520179		GO_Central	GO_REF:0000033

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LCA5L	Human	protein binding	enables	IPI	UniProtKB:P06753 and UniProtKB:Q9UBB9	150520179	PMID:31515488	IntAct	PMID:31515488
LCA5L	Human	protein binding	enables	IPI	UniProtKB:O94868-3 more ...	150520179	PMID:32296183	IntAct	PMID:32296183
LCA5L	Human	protein binding	enables	IPI	UniProtKB:O60333-2 more ...	150520179	PMID:32814053	IntAct	PMID:32814053
LCA5L	Human	protein binding	enables	IPI	UniProtKB:P06753 more ...	150520179	PMID:25416956	IntAct	PMID:25416956

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
LCA5L	Human	Autism		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Autism	ClinVar	PMID:21681106 and PMID:30208311

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:10830953	PMID:12477932	PMID:15489334	PMID:17546029	PMID:21873635	PMID:23455924	PMID:24705354	PMID:25416956	PMID:27100087	PMID:28065597	PMID:28514442	PMID:29676528
PMID:30021884	PMID:31515488	PMID:31586073	PMID:31839598	PMID:32296183	PMID:32393512	PMID:32814053	PMID:33961781	PMID:34349018	PMID:39358380

LCA5L
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	21	39,405,728 - 39,445,805 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	21	40,777,654 - 40,817,704 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	21	39,699,640 - 39,737,998 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	21	39,699,639 - 39,737,998	NCBI
Celera	21	25,975,464 - 26,013,823 (-)	NCBI		Celera
Cytogenetic Map	21	q22.2	NCBI
HuRef	21	26,246,616 - 26,285,006 (-)	NCBI		HuRef
CHM1_1	21	40,338,935 - 40,377,266 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI		T2T-CHM13v2.0

Lca5l
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	16	95,959,605 - 95,993,450 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	16	95,959,607 - 95,993,471 (-)	Ensembl		GRCm39 Ensembl
GRCm38	16	96,158,406 - 96,192,257 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	16	96,158,407 - 96,192,271 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	16	96,380,013 - 96,413,864 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	16	96,263,316 - 96,297,160 (-)	NCBI		MGSCv36	mm8
Celera	16	97,233,064 - 97,266,178 (-)	NCBI		Celera
Cytogenetic Map	16	C4	NCBI
cM Map	16	56.84	NCBI

Lca5l
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	11	48,930,127 - 48,964,613 (-)	NCBI		GRCr8
mRatBN7.2	11	35,460,646 - 35,495,133 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	11	35,461,118 - 35,495,047 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	11	44,118,341 - 44,152,065 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	11	36,789,721 - 36,823,447 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	11	35,935,527 - 35,969,438 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	11	36,512,823 - 36,546,806 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	11	36,512,974 - 36,533,073 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	11	40,043,452 - 40,077,367 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	11	36,468,597 - 36,502,649 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	11	32,977,108 - 33,011,026 (+)	NCBI		Celera
Cytogenetic Map	11	q11	NCBI

Lca5l
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0	NW_004955407	38,176,533 - 38,220,781 (-)	NCBI	ChiLan1.0	ChiLan1.0

LCA5L
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	22	35,496,720 - 35,544,584 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	21	30,352,614 - 30,400,477 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	21	25,759,740 - 25,800,006 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	21	39,096,868 - 39,136,598 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	21	39,096,878 - 39,136,550 (-)	Ensembl	panpan1.1		panPan2

LCA5L
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Dog10K_Boxer_Tasha	31	33,440,102 - 33,489,499 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	31	33,673,870 - 33,723,649 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	31	33,674,611 - 33,696,597 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	31	33,546,233 - 33,595,574 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	31	33,551,217 - 33,600,357 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	31	34,042,392 - 34,091,781 (-)	NCBI		UU_Cfam_GSD_1.0

Lca5l
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024404971	33,657,692 - 33,709,803 (-)	NCBI		HiC_Itri_2
SpeTri2.0	NW_004936500	3,780,622 - 3,809,924 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

LCA5L
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	13	202,988,757 - 203,045,263 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	13	202,988,483 - 203,045,199 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	13	213,156,266 - 213,197,942 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

LCA5L
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	2	83,351,507 - 83,395,096 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	2	83,350,583 - 83,376,491 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666054	11,211,240 - 11,254,983 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Lca5l
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624745	24,595,470 - 24,620,014 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624745	24,578,503 - 24,619,991 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in LCA5L
52 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3	copy number gain	See cases [RCV000050445]	Chr21:7749532..46670405 [GRCh38] Chr21:15499847..48090317 [GRCh37] Chr21:14421718..46914745 [NCBI36] Chr21:21p11.2-q22.3	pathogenic\|conflicting interpretations of pathogenicity\|conflicting data from submitters
GRCh38/hg38 21q22.13-22.3(chr21:37135738-42434515)x1	copy number loss	See cases [RCV000051047]	Chr21:37135738..42434515 [GRCh38] Chr21:38508038..43854625 [GRCh37] Chr21:37429908..42727694 [NCBI36] Chr21:21q22.13-22.3	pathogenic
GRCh37/hg19 21q22.1-22.3(chr21:35527952-44298520)x1	copy number loss	See cases [RCV000052807]	Chr21:35527952..44298520 [GRCh37] Chr21:34449822..43171589 [NCBI36] Chr21:21q22.1-22.3	pathogenic
GRCh38/hg38 21q22.12-22.3(chr21:35027972-46670405)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052836]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052836]\|See cases [RCV000052836]	Chr21:35027972..46670405 [GRCh38] Chr21:36400269..48090317 [GRCh37] Chr21:35322139..46914745 [NCBI36] Chr21:21q22.12-22.3	pathogenic
GRCh38/hg38 21q22.13-22.3(chr21:38273492-46670405)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052838]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052838]\|See cases [RCV000052838]	Chr21:38273492..46670405 [GRCh38] Chr21:39645414..48090317 [GRCh37] Chr21:38567284..46914745 [NCBI36] Chr21:21q22.13-22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3	copy number gain	See cases [RCV000053042]	Chr21:7749532..46623792 [GRCh38] Chr21:14595524..48043704 [GRCh37] Chr21:13517395..46868132 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3	copy number gain	See cases [RCV000053043]	Chr21:7749532..46623792 [GRCh38] Chr21:14629063..48043704 [GRCh37] Chr21:13550934..46868132 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670546)x3	copy number gain	See cases [RCV000053045]	Chr21:7749532..46670546 [GRCh38] Chr21:15499647..48090458 [GRCh37] Chr21:14421518..46914886 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46661140)x3	copy number gain	See cases [RCV000053065]	Chr21:7749532..46661140 [GRCh38] Chr21:15499647..48081052 [GRCh37] Chr21:14421518..46905480 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46661140)x3	copy number gain	See cases [RCV000053067]	Chr21:7749532..46661140 [GRCh38] Chr21:15499847..48081052 [GRCh37] Chr21:14421718..46905480 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3	copy number gain	See cases [RCV000053068]	Chr21:7749532..46670405 [GRCh38] Chr21:20655360..48090317 [GRCh37] Chr21:19577231..46914745 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3	copy number gain	See cases [RCV000053069]	Chr21:7749532..46670405 [GRCh38] Chr21:34423268..48090317 [GRCh37] Chr21:33345138..46914745 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3	copy number gain	See cases [RCV000053039]	Chr21:7749532..46623792 [GRCh38] Chr21:14524963..48043704 [GRCh37] Chr21:13446834..46868132 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46653090)x3	copy number gain	See cases [RCV000053040]	Chr21:7749532..46653090 [GRCh38] Chr21:14539679..48073002 [GRCh37] Chr21:13461550..46897430 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh37/hg19 21q22.13-22.2(chr21:37839410..41427526)	copy number loss	DYRK1A-related intellectual disability syndrome [RCV000190476]	Chr21:37839410..41427526 [GRCh37] Chr21:21q22.13-22.2	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-42971047)x3	copy number gain	See cases [RCV000133676]	Chr21:7749532..42971047 [GRCh38] Chr21:15499847..44391157 [GRCh37] Chr21:14421718..43264226 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46653084)x3	copy number gain	See cases [RCV000134727]	Chr21:7749532..46653084 [GRCh38] Chr21:15485038..48072996 [GRCh37] Chr21:14406909..46897424 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46649831)x3	copy number gain	See cases [RCV000134509]	Chr21:7749532..46649831 [GRCh38] Chr21:14577835..48069743 [GRCh37] Chr21:13499706..46894171 [NCBI36] Chr21:21q11.2-22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670440)x3	copy number gain	See cases [RCV000134119]	Chr21:7749532..46670440 [GRCh38] Chr21:15485038..48090352 [GRCh37] Chr21:14406909..46914780 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21q22.11-22.3(chr21:7749532-46670346)x3	copy number gain	See cases [RCV000135310]	Chr21:7749532..46670346 [GRCh38] Chr21:34111831..48090258 [GRCh37] Chr21:33033702..46914686 [NCBI36] Chr21:21q22.11-22.3	pathogenic
GRCh38/hg38 21q22.12-22.3(chr21:36206067-46670405)x3	copy number gain	See cases [RCV000134972]	Chr21:36206067..46670405 [GRCh38] Chr21:37578365..48090317 [GRCh37] Chr21:36500235..46914745 [NCBI36] Chr21:21q22.12-22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46664250)x3	copy number gain	See cases [RCV000134836]	Chr21:7749532..46664250 [GRCh38] Chr21:15485038..48084162 [GRCh37] Chr21:14406909..46908590 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670440)x3	copy number gain	See cases [RCV000134842]	Chr21:7749532..46670440 [GRCh38] Chr21:15513244..48090352 [GRCh37] Chr21:14435115..46914780 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46660999)x3	copy number gain	See cases [RCV000135448]	Chr21:7749532..46660999 [GRCh38] Chr21:15499847..48080911 [GRCh37] Chr21:14421718..46905339 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21q22.12-22.2(chr21:35543872-39993338)x1	copy number loss	See cases [RCV000135412]	Chr21:35543872..39993338 [GRCh38] Chr21:36916169..41365265 [GRCh37] Chr21:35838039..40287135 [NCBI36] Chr21:21q22.12-22.2	pathogenic
GRCh38/hg38 21q22.13-22.3(chr21:36519173-46670405)x3	copy number gain	See cases [RCV000136142]	Chr21:36519173..46670405 [GRCh38] Chr21:37891471..48090317 [GRCh37] Chr21:36813341..46914745 [NCBI36] Chr21:21q22.13-22.3	pathogenic
GRCh38/hg38 21q22.12-22.3(chr21:34789953-46636538)x1	copy number loss	See cases [RCV000136828]	Chr21:34789953..46636538 [GRCh38] Chr21:36162250..48056450 [GRCh37] Chr21:35084120..46880878 [NCBI36] Chr21:21q22.12-22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3	copy number gain	See cases [RCV000137337]	Chr21:7749532..46671060 [GRCh38] Chr21:10697897..48090972 [GRCh37] Chr21:1..46915400 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3	copy number gain	See cases [RCV000137255]	Chr21:7749532..46671060 [GRCh38] Chr21:35319225..48090972 [GRCh37] Chr21:34241095..46915400 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3	copy number gain	See cases [RCV000138216]	Chr21:7749532..46671060 [GRCh38] Chr21:10944001..48090972 [GRCh37] Chr21:9965872..46915400 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21q22.13-22.3(chr21:37669628-46671060)x1	copy number loss	See cases [RCV000138096]	Chr21:37669628..46671060 [GRCh38] Chr21:39041930..48090972 [GRCh37] Chr21:37963800..46915400 [NCBI36] Chr21:21q22.13-22.3	pathogenic
GRCh38/hg38 21q22.12-22.3(chr21:36066991-46671060)x3	copy number gain	See cases [RCV000138164]	Chr21:36066991..46671060 [GRCh38] Chr21:37439289..48090972 [GRCh37] Chr21:36361159..46915400 [NCBI36] Chr21:21q22.12-22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3	copy number gain	See cases [RCV000138436]	Chr21:7749532..46671060 [GRCh38] Chr21:15451032..48090972 [GRCh37] Chr21:14372903..46915400 [NCBI36] Chr21:21p11.2-q22.3	pathogenic\|conflicting data from submitters
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46670346)x3	copy number gain	See cases [RCV000140103]	Chr21:7749532..46670346 [GRCh38] Chr21:14577894..48090258 [GRCh37] Chr21:13499765..46914686 [NCBI36] Chr21:21q11.2-22.3	pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46698247)x3	copy number gain	See cases [RCV000141346]	Chr21:7749532..46698247 [GRCh38] Chr21:14577835..48118159 [GRCh37] Chr21:13499706..46942587 [NCBI36] Chr21:21q11.2-22.3	pathogenic
GRCh38/hg38 21q21.3-22.3(chr21:7749532-46677460)x3	copy number gain	See cases [RCV000141827]	Chr21:7749532..46677460 [GRCh38] Chr21:28285299..48097372 [GRCh37] Chr21:27207170..46921800 [NCBI36] Chr21:21q21.3-22.3	uncertain significance
GRCh38/hg38 21q22.2-22.3(chr21:38816399-46677460)x1	copy number loss	See cases [RCV000142311]	Chr21:38816399..46677460 [GRCh38] Chr21:40188323..48097372 [GRCh37] Chr21:39110193..46921800 [NCBI36] Chr21:21q22.2-22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7817158-46670440)x1	copy number loss	See cases [RCV000142427]	Chr21:7817158..46670440 [GRCh38] Chr21:15485038..48090352 [GRCh37] Chr21:14406909..46914780 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh38/hg38 21q22.2-22.3(chr21:39375937-44246148)x1	copy number loss	See cases [RCV000142650]	Chr21:39375937..44246148 [GRCh38] Chr21:40747863..45666031 [GRCh37] Chr21:39669733..44490459 [NCBI36] Chr21:21q22.2-22.3	pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460)x3	copy number gain	See cases [RCV000143376]	Chr21:7749532..46677460 [GRCh38] Chr21:15006458..48097372 [GRCh37] Chr21:13928329..46921800 [NCBI36] Chr21:21q11.2-22.3	pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460)	copy number gain	See cases [RCV000143160]	Chr21:7749532..46677460 [GRCh38] Chr21:14386013..48097372 [GRCh37] Chr21:13307884..46921800 [NCBI36] Chr21:21q11.2-22.3	pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460)x3	copy number gain	See cases [RCV000143120]	Chr21:7749532..46677460 [GRCh38] Chr21:15006457..48097372 [GRCh37] Chr21:13928328..46921800 [NCBI36] Chr21:21q11.2-22.3	pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3	copy number gain	See cases [RCV000148131]	Chr21:7749532..46670405 [GRCh38] Chr21:15499847..48090317 [GRCh37] Chr21:14421718..46914745 [NCBI36] Chr21:21p11.2-q22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15538655-48080926)x1	copy number loss	See cases [RCV000239948]	Chr21:15538655..48080926 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q22.2-22.3(chr21:39841248-44652723)x3	copy number gain	See cases [RCV000239953]	Chr21:39841248..44652723 [GRCh37] Chr21:21q22.2-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15410701-48090317)x3	copy number gain	See cases [RCV000240397]	Chr21:15410701..48090317 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q22.2(chr21:40802860-41301131)x3	copy number gain	See cases [RCV000240283]	Chr21:40802860..41301131 [GRCh37] Chr21:21q22.2	uncertain significance
GRCh37/hg19 21q22.13-22.2(chr21:38176362-41901945)x1	copy number loss	See cases [RCV000449183]	Chr21:38176362..41901945 [GRCh37] Chr21:21q22.13-22.2	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-43598570)x3	copy number gain	See cases [RCV000446716]	Chr21:15006457..43598570 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q22.13-22.3(chr21:38790552-43619940)x1	copy number loss	See cases [RCV000446516]	Chr21:38790552..43619940 [GRCh37] Chr21:21q22.13-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:14771770-48080867)x3	copy number gain	See cases [RCV000447884]	Chr21:14771770..48080867 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15285841-48097372)x3	copy number gain	See cases [RCV000447729]	Chr21:15285841..48097372 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-44827632)x3	copy number gain	See cases [RCV000448199]	Chr21:15006457..44827632 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3	copy number gain	See cases [RCV000447749]	Chr21:15006457..48097372 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q22.13-22.3(chr21:38699545-48097372)x1	copy number loss	See cases [RCV000510684]	Chr21:38699545..48097372 [GRCh37] Chr21:21q22.13-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006458-48097372)	copy number gain	See cases [RCV000511589]	Chr21:15006458..48097372 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q22.13-22.3(chr21:37914123-48097372)x1	copy number loss	See cases [RCV000510798]	Chr21:37914123..48097372 [GRCh37] Chr21:21q22.13-22.3	pathogenic
GRCh37/hg19 21q22.12-22.2(chr21:36183329-42311538)x3	copy number gain	See cases [RCV000512585]	Chr21:36183329..42311538 [GRCh37] Chr21:21q22.12-22.2	likely pathogenic
GRCh37/hg19 21q22.11-22.2(chr21:33980213-42542987)x3	copy number gain	not provided [RCV000684166]	Chr21:33980213..42542987 [GRCh37] Chr21:21q22.11-22.2	pathogenic
GRCh37/hg19 21q22.2(chr21:40039202-41278694)x1	copy number loss	not provided [RCV000684157]	Chr21:40039202..41278694 [GRCh37] Chr21:21q22.2	uncertain significance
NC_000021.9:g.(?_38981673)_(41568791_?)del	deletion	Autism [RCV000754228]	Chr21:38981673..41568791 [GRCh38] Chr21:21q22.2-22.3	likely pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10827533-48100155)x3	copy number gain	not provided [RCV000741419]	Chr21:10827533..48100155 [GRCh37] Chr21:21p11.2-q22.3	pathogenic
GRCh37/hg19 21q22.2-22.3(chr21:40364245-44169928)x1	copy number loss	not provided [RCV000741567]	Chr21:40364245..44169928 [GRCh37] Chr21:21q22.2-22.3	pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10699330-48117896)x3	copy number gain	not provided [RCV000741413]	Chr21:10699330..48117896 [GRCh37] Chr21:21p11.2-q22.3	pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10704198-48117896)x3	copy number gain	not provided [RCV000741415]	Chr21:10704198..48117896 [GRCh37] Chr21:21p11.2-q22.3	pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10824040-48090629)x3	copy number gain	not provided [RCV000741418]	Chr21:10824040..48090629 [GRCh37] Chr21:21p11.2-q22.3	pathogenic
GRCh37/hg19 21q22.2(chr21:40726882-41265009)x3	copy number gain	not provided [RCV000849872]	Chr21:40726882..41265009 [GRCh37] Chr21:21q22.2	uncertain significance
GRCh37/hg19 21q22.2(chr21:40726882-41265009)x3	copy number gain	not provided [RCV000849873]	Chr21:40726882..41265009 [GRCh37] Chr21:21q22.2	uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3	copy number gain	not provided [RCV000846937]	Chr21:15006457..48097372 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q22.2(chr21:40067081-40841948)x3	copy number gain	not provided [RCV000848786]	Chr21:40067081..40841948 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.994G>C (p.Glu332Gln)	single nucleotide variant	not specified [RCV004316650]	Chr21:39411784 [GRCh38] Chr21:40783710 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.545A>G (p.His182Arg)	single nucleotide variant	not specified [RCV004292354]	Chr21:39423268 [GRCh38] Chr21:40795194 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.45C>A (p.Phe15Leu)	single nucleotide variant	not specified [RCV004289331]	Chr21:39428449 [GRCh38] Chr21:40800375 [GRCh37] Chr21:21q22.2	uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:14420615-48080926)x3	copy number gain	Down syndrome [RCV002284306]	Chr21:14420615..48080926 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q22.13-22.3(chr21:39410438-45171756)x1	copy number loss	not provided [RCV001007132]	Chr21:39410438..45171756 [GRCh37] Chr21:21q22.13-22.3	pathogenic
GRCh37/hg19 21q22.13-22.2(chr21:39270345-41091831)x1	copy number loss	not provided [RCV001259411]	Chr21:39270345..41091831 [GRCh37] Chr21:21q22.13-22.2	uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:14629063-48090317)x3	copy number gain	See cases [RCV001263025]	Chr21:14629063..48090317 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21p13-q22.3(chr21:1-48129895)x3	copy number gain	See cases [RCV001780078]	Chr21:1..48129895 [GRCh37] Chr21:21p13-q22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15041209-48097372)	copy number gain	not specified [RCV002052724]	Chr21:15041209..48097372 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15285841-48097372)	copy number gain	not specified [RCV002052725]	Chr21:15285841..48097372 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q22.2(chr21:39892114-40905632)x1	copy number loss	not provided [RCV001836600]	Chr21:39892114..40905632 [GRCh37] Chr21:21q22.2	uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3	copy number gain	not provided [RCV001829203]	Chr21:15006457..48097372 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)	copy number gain	not specified [RCV002052723]	Chr21:15006457..48097372 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q22.2(chr21:40219284-41569839)x3	copy number gain	not provided [RCV002472434]	Chr21:40219284..41569839 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.38A>C (p.Glu13Ala)	single nucleotide variant	not specified [RCV004117348]	Chr21:39428456 [GRCh38] Chr21:40800382 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1202A>G (p.Lys401Arg)	single nucleotide variant	not specified [RCV004187174]	Chr21:39410059 [GRCh38] Chr21:40781985 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1936G>A (p.Gly646Arg)	single nucleotide variant	not specified [RCV004111175]	Chr21:39405959 [GRCh38] Chr21:40777885 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.632G>C (p.Arg211Thr)	single nucleotide variant	not specified [RCV004188355]	Chr21:39423181 [GRCh38] Chr21:40795107 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1151C>G (p.Pro384Arg)	single nucleotide variant	not specified [RCV004182143]	Chr21:39410277 [GRCh38] Chr21:40782203 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.784C>G (p.His262Asp)	single nucleotide variant	not specified [RCV004084370]	Chr21:39423029 [GRCh38] Chr21:40794955 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1193A>C (p.His398Pro)	single nucleotide variant	not specified [RCV004245495]	Chr21:39410068 [GRCh38] Chr21:40781994 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.118C>T (p.Arg40Trp)	single nucleotide variant	not specified [RCV004163095]	Chr21:39428376 [GRCh38] Chr21:40800302 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.764C>G (p.Ala255Gly)	single nucleotide variant	not specified [RCV004102664]	Chr21:39423049 [GRCh38] Chr21:40794975 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1796T>C (p.Met599Thr)	single nucleotide variant	not specified [RCV004201028]	Chr21:39406099 [GRCh38] Chr21:40778025 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1337G>C (p.Gly446Ala)	single nucleotide variant	not specified [RCV004199445]	Chr21:39406558 [GRCh38] Chr21:40778484 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1502G>C (p.Gly501Ala)	single nucleotide variant	not specified [RCV004224102]	Chr21:39406393 [GRCh38] Chr21:40778319 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1470A>C (p.Arg490Ser)	single nucleotide variant	not specified [RCV004167087]	Chr21:39406425 [GRCh38] Chr21:40778351 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1985C>T (p.Thr662Ile)	single nucleotide variant	not specified [RCV004169762]	Chr21:39405910 [GRCh38] Chr21:40777836 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1541C>T (p.Thr514Met)	single nucleotide variant	not specified [RCV004180561]	Chr21:39406354 [GRCh38] Chr21:40778280 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.957C>A (p.His319Gln)	single nucleotide variant	not specified [RCV004174019]	Chr21:39420724 [GRCh38] Chr21:40792650 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.425G>A (p.Arg142Gln)	single nucleotide variant	not specified [RCV004086518]	Chr21:39423388 [GRCh38] Chr21:40795314 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1882A>G (p.Ser628Gly)	single nucleotide variant	not specified [RCV004260119]	Chr21:39406013 [GRCh38] Chr21:40777939 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1175C>T (p.Ala392Val)	single nucleotide variant	not specified [RCV004280150]	Chr21:39410086 [GRCh38] Chr21:40782012 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.974A>T (p.Lys325Met)	single nucleotide variant	not specified [RCV004277205]	Chr21:39420707 [GRCh38] Chr21:40792633 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1174G>A (p.Ala392Thr)	single nucleotide variant	not specified [RCV004280149]	Chr21:39410087 [GRCh38] Chr21:40782013 [GRCh37] Chr21:21q22.2	likely benign
NM_152505.4(LCA5L):c.274G>C (p.Glu92Gln)	single nucleotide variant	not specified [RCV004325788]	Chr21:39428220 [GRCh38] Chr21:40800146 [GRCh37] Chr21:21q22.2	uncertain significance
GRCh37/hg19 21q22.2-22.3(chr21:40681179-48097372)x1	copy number loss	not provided [RCV003483381]	Chr21:40681179..48097372 [GRCh37] Chr21:21q22.2-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006458-45674637)x3	copy number gain	not provided [RCV003485218]	Chr21:15006458..45674637 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q22.11-22.3(chr21:33015681-48097372)x3	copy number gain	not provided [RCV003485222]	Chr21:33015681..48097372 [GRCh37] Chr21:21q22.11-22.3	pathogenic
NM_152505.4(LCA5L):c.1722T>C (p.Tyr574=)	single nucleotide variant	not provided [RCV003431500]	Chr21:39406173 [GRCh38] Chr21:40778099 [GRCh37] Chr21:21q22.2	likely benign
NM_152505.4(LCA5L):c.1536C>G (p.Pro512=)	single nucleotide variant	not provided [RCV003431501]	Chr21:39406359 [GRCh38] Chr21:40778285 [GRCh37] Chr21:21q22.2	likely benign
NM_152505.4(LCA5L):c.1863C>G (p.Gly621=)	single nucleotide variant	not provided [RCV003431499]	Chr21:39406032 [GRCh38] Chr21:40777958 [GRCh37] Chr21:21q22.2	likely benign
GRCh37/hg19 21q22.11-22.3(chr21:34092685-48097372)x3	copy number gain	not specified [RCV003986158]	Chr21:34092685..48097372 [GRCh37] Chr21:21q22.11-22.3	pathogenic
GRCh37/hg19 21q21.3-22.3(chr21:26929299-48097372)x3	copy number gain	not specified [RCV003986152]	Chr21:26929299..48097372 [GRCh37] Chr21:21q21.3-22.3	pathogenic
GRCh37/hg19 21q22.12-22.3(chr21:35872675-48097372)x1	copy number loss	not specified [RCV003986157]	Chr21:35872675..48097372 [GRCh37] Chr21:21q22.12-22.3	pathogenic
GRCh37/hg19 21q21.3-22.3(chr21:30685776-48097372)x3	copy number gain	not specified [RCV003986149]	Chr21:30685776..48097372 [GRCh37] Chr21:21q21.3-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15023401-48097372)x3	copy number gain	not specified [RCV003986160]	Chr21:15023401..48097372 [GRCh37] Chr21:21q11.2-22.3	pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15380398-48100790)x3	copy number gain	not provided [RCV004577449]	Chr21:15380398..48100790 [GRCh37] Chr21:21q11.2-22.3	pathogenic
NM_152505.4(LCA5L):c.101G>A (p.Gly34Asp)	single nucleotide variant	not specified [RCV004410325]	Chr21:39428393 [GRCh38] Chr21:40800319 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1258G>A (p.Glu420Lys)	single nucleotide variant	not specified [RCV004410326]	Chr21:39410003 [GRCh38] Chr21:40781929 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1585G>C (p.Ala529Pro)	single nucleotide variant	not specified [RCV004410327]	Chr21:39406310 [GRCh38] Chr21:40778236 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.160T>G (p.Ser54Ala)	single nucleotide variant	not specified [RCV004410328]	Chr21:39428334 [GRCh38] Chr21:40800260 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.290A>G (p.Lys97Arg)	single nucleotide variant	not specified [RCV004410329]	Chr21:39428204 [GRCh38] Chr21:40800130 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.293A>G (p.Tyr98Cys)	single nucleotide variant	not specified [RCV004410330]	Chr21:39428201 [GRCh38] Chr21:40800127 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.198T>G (p.Asp66Glu)	single nucleotide variant	not specified [RCV004633895]	Chr21:39428296 [GRCh38] Chr21:40800222 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1124A>G (p.Gln375Arg)	single nucleotide variant	not specified [RCV004642151]	Chr21:39410304 [GRCh38] Chr21:40782230 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.743T>C (p.Leu248Pro)	single nucleotide variant	not specified [RCV004642152]	Chr21:39423070 [GRCh38] Chr21:40794996 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1136A>C (p.Lys379Thr)	single nucleotide variant	not specified [RCV004939879]	Chr21:39410292 [GRCh38] Chr21:40782218 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1717G>A (p.Gly573Arg)	single nucleotide variant	not specified [RCV004939881]	Chr21:39406178 [GRCh38] Chr21:40778104 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1055C>G (p.Pro352Arg)	single nucleotide variant	not specified [RCV004939883]	Chr21:39411723 [GRCh38] Chr21:40783649 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.52G>A (p.Val18Met)	single nucleotide variant	not specified [RCV004939878]	Chr21:39428442 [GRCh38] Chr21:40800368 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1928A>G (p.His643Arg)	single nucleotide variant	not specified [RCV004939882]	Chr21:39405967 [GRCh38] Chr21:40777893 [GRCh37] Chr21:21q22.2	uncertain significance
GRCh37/hg19 21q22.11-22.3(chr21:34586759-48097372)x3	copy number gain	not provided [RCV004819321]	Chr21:34586759..48097372 [GRCh37] Chr21:21q22.11-22.3	pathogenic
NM_152505.4(LCA5L):c.625A>C (p.Asn209His)	single nucleotide variant	not specified [RCV004939885]	Chr21:39423188 [GRCh38] Chr21:40795114 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1823T>A (p.Val608Asp)	single nucleotide variant	not specified [RCV004939880]	Chr21:39406072 [GRCh38] Chr21:40777998 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1502G>T (p.Gly501Val)	single nucleotide variant	not specified [RCV004934862]	Chr21:39406393 [GRCh38] Chr21:40778319 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1976C>T (p.Ser659Leu)	single nucleotide variant	not specified [RCV004934863]	Chr21:39405919 [GRCh38] Chr21:40777845 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.955C>T (p.His319Tyr)	single nucleotide variant	not specified [RCV004412403]	Chr21:39420726 [GRCh38] Chr21:40792652 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.1630G>A (p.Ala544Thr)	single nucleotide variant	not specified [RCV004329590]	Chr21:39406265 [GRCh38] Chr21:40778191 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.676A>T (p.Arg226Trp)	single nucleotide variant	not specified [RCV004410331]	Chr21:39423137 [GRCh38] Chr21:40795063 [GRCh37] Chr21:21q22.2	uncertain significance
NM_152505.4(LCA5L):c.806C>T (p.Thr269Ile)	single nucleotide variant	not specified [RCV004410332]	Chr21:39423007 [GRCh38] Chr21:40794933 [GRCh37] Chr21:21q22.2	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	2325
Count of miRNA genes:	916
Interacting mature miRNAs:	1070
Transcripts:	ENST00000288350, ENST00000358268, ENST00000380671, ENST00000411566, ENST00000415863, ENST00000418018, ENST00000426783, ENST00000434281, ENST00000438404, ENST00000448288, ENST00000451131, ENST00000456017, ENST00000459939, ENST00000466954, ENST00000468009, ENST00000480612, ENST00000484878, ENST00000485895, ENST00000490184, ENST00000491625, ENST00000495240
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597348232	GWAS1444306_H	systolic blood pressure QTL GWAS1444306 (human)		0.000005	systolic blood pressure	systolic blood pressure (CMO:0000004)	21	39445776	39445777	Human
597115681	GWAS1211755_H	pulse pressure measurement QTL GWAS1211755 (human)		1e-09	pulse pressure measurement	pulse pressure (CMO:0000292)	21	39445776	39445777	Human
2303081	MAMTS49_H	Mammary tumor susceptibility QTL 49 (human)	1.72		Mammary tumor susceptibility		21	17950448	43950448	Human
597359253	GWAS1455327_H	venous thromboembolism QTL GWAS1455327 (human)		0.000009	venous thromboembolism		21	39417758	39417759	Human

RH94177

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,800,236 - 40,800,358	UniSTS	GRCh37
Build 36	21	39,722,106 - 39,722,228	RGD	NCBI36
Celera	21	25,997,932 - 25,998,054	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,269,093 - 26,269,215	UniSTS

SHGC-6832

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,799,095 - 40,799,201	UniSTS	GRCh37
Build 36	21	39,720,965 - 39,721,071	RGD	NCBI36
Celera	21	25,996,791 - 25,996,897	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,267,952 - 26,268,058	UniSTS
TNG Radiation Hybrid Map	21	15106.0	UniSTS

PMC310729P1

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,780,587 - 40,780,746	UniSTS	GRCh37
Build 36	21	39,702,457 - 39,702,616	RGD	NCBI36
Celera	21	25,978,281 - 25,978,440	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,249,433 - 26,249,592	UniSTS

ECD05253

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,799,631 - 40,800,371	UniSTS	GRCh37
Build 36	21	39,721,501 - 39,722,241	RGD	NCBI36
Celera	21	25,997,327 - 25,998,067	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,268,488 - 26,269,228	UniSTS

ECD05296

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,800,868 - 40,801,607	UniSTS	GRCh37
Build 36	21	39,722,738 - 39,723,477	RGD	NCBI36
Celera	21	25,998,564 - 25,999,303	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,269,747 - 26,270,486	UniSTS

ECD06432

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,784,244 - 40,784,952	UniSTS	GRCh37
Build 36	21	39,706,114 - 39,706,822	RGD	NCBI36
Celera	21	25,981,938 - 25,982,646	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,253,090 - 26,253,798	UniSTS

ECD06780

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,785,699 - 40,786,398	UniSTS	GRCh37
Build 36	21	39,707,569 - 39,708,268	RGD	NCBI36
Celera	21	25,983,393 - 25,984,092	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,254,545 - 26,255,244	UniSTS

ECD07620

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,794,826 - 40,795,502	UniSTS	GRCh37
Build 36	21	39,716,696 - 39,717,372	RGD	NCBI36
Celera	21	25,992,522 - 25,993,198	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,263,683 - 26,264,359	UniSTS

ECD07695

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,794,081 - 40,794,755	UniSTS	GRCh37
Build 36	21	39,715,951 - 39,716,625	RGD	NCBI36
Celera	21	25,991,777 - 25,992,451	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,262,941 - 26,263,612	UniSTS

ECD07729

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,793,315 - 40,793,988	UniSTS	GRCh37
Build 36	21	39,715,185 - 39,715,858	RGD	NCBI36
Celera	21	25,991,011 - 25,991,684	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,262,175 - 26,262,848	UniSTS

ECD08030

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,784,971 - 40,785,636	UniSTS	GRCh37
Build 36	21	39,706,841 - 39,707,506	RGD	NCBI36
Celera	21	25,982,665 - 25,983,330	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,253,817 - 26,254,482	UniSTS

ECD08392

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,803,760 - 40,804,415	UniSTS	GRCh37
Build 36	21	39,725,630 - 39,726,285	RGD	NCBI36
Celera	21	26,001,456 - 26,002,111	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,272,639 - 26,273,294	UniSTS

ECD08894

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,783,368 - 40,784,010	UniSTS	GRCh37
Build 36	21	39,705,238 - 39,705,880	RGD	NCBI36
Celera	21	25,981,062 - 25,981,704	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,252,214 - 26,252,856	UniSTS

ECD09713

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,806,797 - 40,807,418	UniSTS	GRCh37
Build 36	21	39,728,667 - 39,729,288	RGD	NCBI36
Celera	21	26,004,492 - 26,005,113	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,275,675 - 26,276,296	UniSTS

ECD10065

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,817,009 - 40,817,620	UniSTS	GRCh37
Build 36	21	39,738,879 - 39,739,490	RGD	NCBI36
Celera	21	26,014,704 - 26,015,318	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,285,887 - 26,286,498	UniSTS

ECD10321

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,797,096 - 40,797,700	UniSTS	GRCh37
Build 36	21	39,718,966 - 39,719,570	RGD	NCBI36
Celera	21	25,994,792 - 25,995,396	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,265,953 - 26,266,557	UniSTS

ECD10322

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,797,727 - 40,798,331	UniSTS	GRCh37
Build 36	21	39,719,597 - 39,720,201	RGD	NCBI36
Celera	21	25,995,423 - 25,996,027	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,266,584 - 26,267,188	UniSTS

ECD11691

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,798,714 - 40,799,278	UniSTS	GRCh37
Build 36	21	39,720,584 - 39,721,148	RGD	NCBI36
Celera	21	25,996,410 - 25,996,974	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,267,571 - 26,268,135	UniSTS

ECD11826

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,813,246 - 40,813,806	UniSTS	GRCh37
Build 36	21	39,735,116 - 39,735,676	RGD	NCBI36
Celera	21	26,010,941 - 26,011,501	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,282,124 - 26,282,684	UniSTS

ECD11864

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,802,863 - 40,803,422	UniSTS	GRCh37
Build 36	21	39,724,733 - 39,725,292	RGD	NCBI36
Celera	21	26,000,559 - 26,001,118	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,271,742 - 26,272,301	UniSTS

ECD12626

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,805,904 - 40,806,442	UniSTS	GRCh37
Build 36	21	39,727,774 - 39,728,312	RGD	NCBI36
Celera	21	26,003,599 - 26,004,137	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,274,782 - 26,275,320	UniSTS

ECD13158

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,807,865 - 40,808,389	UniSTS	GRCh37
Build 36	21	39,729,735 - 39,730,259	RGD	NCBI36
Celera	21	26,005,560 - 26,006,084	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,276,743 - 26,277,267	UniSTS

ECD13954

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,777,829 - 40,778,333	UniSTS	GRCh37
Build 36	21	39,699,699 - 39,700,203	RGD	NCBI36
Celera	21	25,975,523 - 25,976,027	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,246,675 - 26,247,179	UniSTS

ECD14159

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,792,497 - 40,792,996	UniSTS	GRCh37
Build 36	21	39,714,367 - 39,714,866	RGD	NCBI36
Celera	21	25,990,193 - 25,990,692	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,261,357 - 26,261,856	UniSTS

ECD14253

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,778,368 - 40,778,865	UniSTS	GRCh37
Build 36	21	39,700,238 - 39,700,735	RGD	NCBI36
Celera	21	25,976,062 - 25,976,559	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,247,214 - 26,247,711	UniSTS

ECD16640

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,782,479 - 40,782,910	UniSTS	GRCh37
Build 36	21	39,704,349 - 39,704,780	RGD	NCBI36
Celera	21	25,980,173 - 25,980,604	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,251,325 - 26,251,756	UniSTS

ECD16701

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,780,425 - 40,780,853	UniSTS	GRCh37
Build 36	21	39,702,295 - 39,702,723	RGD	NCBI36
Celera	21	25,978,119 - 25,978,547	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,249,271 - 26,249,699	UniSTS

ECD17137

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,816,080 - 40,816,491	UniSTS	GRCh37
Build 36	21	39,737,950 - 39,738,361	RGD	NCBI36
Celera	21	26,013,775 - 26,014,186	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,284,958 - 26,285,369	UniSTS

ECD17606

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,781,917 - 40,782,308	UniSTS	GRCh37
Build 36	21	39,703,787 - 39,704,178	RGD	NCBI36
Celera	21	25,979,611 - 25,980,002	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,250,763 - 26,251,154	UniSTS

ECD18059

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,801,987 - 40,802,361	UniSTS	GRCh37
Build 36	21	39,723,857 - 39,724,231	RGD	NCBI36
Celera	21	25,999,683 - 26,000,057	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,270,866 - 26,271,240	UniSTS

ECD19065

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,779,718 - 40,780,053	UniSTS	GRCh37
Build 36	21	39,701,588 - 39,701,923	RGD	NCBI36
Celera	21	25,977,412 - 25,977,747	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,248,564 - 26,248,899	UniSTS

ECD19525

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,790,823 - 40,791,141	UniSTS	GRCh37
Build 36	21	39,712,693 - 39,713,011	RGD	NCBI36
Celera	21	25,988,517 - 25,988,835	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,259,675 - 26,259,993	UniSTS

ECD19849

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,811,469 - 40,811,775	UniSTS	GRCh37
Build 36	21	39,733,339 - 39,733,645	RGD	NCBI36
Celera	21	26,009,164 - 26,009,470	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,280,347 - 26,280,653	UniSTS

ECD20340

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,777,479 - 40,777,766	UniSTS	GRCh37
Build 36	21	39,699,349 - 39,699,636	RGD	NCBI36
Celera	21	25,975,173 - 25,975,460	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,246,325 - 26,246,612	UniSTS

ECD24228

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,796,583 - 40,796,733	UniSTS	GRCh37
Build 36	21	39,718,453 - 39,718,603	RGD	NCBI36
Celera	21	25,994,279 - 25,994,429	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,265,440 - 26,265,590	UniSTS

SHGC-32517

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,807,952 - 40,808,053	UniSTS	GRCh37
Build 36	21	39,729,822 - 39,729,923	RGD	NCBI36
Celera	21	26,005,647 - 26,005,748	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,276,830 - 26,276,931	UniSTS
TNG Radiation Hybrid Map	21	15098.0	UniSTS
Stanford-G3 RH Map	21	1324.0	UniSTS
Whitehead-RH Map	21	191.3	UniSTS
NCBI RH Map	21	329.7	UniSTS
GeneMap99-G3 RH Map	21	1324.0	UniSTS

REN20453

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,777,391 - 40,777,627	UniSTS	GRCh37
Build 36	21	39,699,261 - 39,699,497	RGD	NCBI36
Celera	21	25,975,085 - 25,975,321	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,246,237 - 26,246,473	UniSTS

REN20454

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,777,603 - 40,777,854	UniSTS	GRCh37
Build 36	21	39,699,473 - 39,699,724	RGD	NCBI36
Celera	21	25,975,297 - 25,975,548	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,246,449 - 26,246,700	UniSTS

REN20455

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,777,832 - 40,778,083	UniSTS	GRCh37
Build 36	21	39,699,702 - 39,699,953	RGD	NCBI36
Celera	21	25,975,526 - 25,975,777	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,246,678 - 26,246,929	UniSTS

REN20456

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,778,080 - 40,778,342	UniSTS	GRCh37
Build 36	21	39,699,950 - 39,700,212	RGD	NCBI36
Celera	21	25,975,774 - 25,976,036	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,246,926 - 26,247,188	UniSTS

REN20457

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,778,319 - 40,778,588	UniSTS	GRCh37
Build 36	21	39,700,189 - 39,700,458	RGD	NCBI36
Celera	21	25,976,013 - 25,976,282	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,247,165 - 26,247,434	UniSTS

REN20458

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,778,577 - 40,778,816	UniSTS	GRCh37
Build 36	21	39,700,447 - 39,700,686	RGD	NCBI36
Celera	21	25,976,271 - 25,976,510	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,247,423 - 26,247,662	UniSTS

REN20459

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,778,787 - 40,779,044	UniSTS	GRCh37
Build 36	21	39,700,657 - 39,700,914	RGD	NCBI36
Celera	21	25,976,481 - 25,976,738	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,247,633 - 26,247,890	UniSTS

REN20460

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,779,017 - 40,779,266	UniSTS	GRCh37
Build 36	21	39,700,887 - 39,701,136	RGD	NCBI36
Celera	21	25,976,711 - 25,976,960	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,247,863 - 26,248,112	UniSTS

REN20461

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,779,260 - 40,779,511	UniSTS	GRCh37
Build 36	21	39,701,130 - 39,701,381	RGD	NCBI36
Celera	21	25,976,954 - 25,977,205	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,248,106 - 26,248,357	UniSTS

REN20462

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,779,495 - 40,779,742	UniSTS	GRCh37
Build 36	21	39,701,365 - 39,701,612	RGD	NCBI36
Celera	21	25,977,189 - 25,977,436	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,248,341 - 26,248,588	UniSTS

REN20463

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,779,718 - 40,779,950	UniSTS	GRCh37
Build 36	21	39,701,588 - 39,701,820	RGD	NCBI36
Celera	21	25,977,412 - 25,977,644	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,248,564 - 26,248,796	UniSTS

REN20464

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,779,914 - 40,780,149	UniSTS	GRCh37
Build 36	21	39,701,784 - 39,702,019	RGD	NCBI36
Celera	21	25,977,608 - 25,977,843	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,248,760 - 26,248,995	UniSTS

REN20465

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,780,126 - 40,780,374	UniSTS	GRCh37
Build 36	21	39,701,996 - 39,702,244	RGD	NCBI36
Celera	21	25,977,820 - 25,978,068	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,248,972 - 26,249,220	UniSTS

REN20466

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,780,351 - 40,780,595	UniSTS	GRCh37
Build 36	21	39,702,221 - 39,702,465	RGD	NCBI36
Celera	21	25,978,045 - 25,978,289	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,249,197 - 26,249,441	UniSTS

REN20467

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,780,586 - 40,780,856	UniSTS	GRCh37
Build 36	21	39,702,456 - 39,702,726	RGD	NCBI36
Celera	21	25,978,280 - 25,978,550	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,249,432 - 26,249,702	UniSTS

REN20468

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,780,833 - 40,781,085	UniSTS	GRCh37
Build 36	21	39,702,703 - 39,702,955	RGD	NCBI36
Celera	21	25,978,527 - 25,978,779	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,249,679 - 26,249,931	UniSTS

REN20469

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,781,035 - 40,781,271	UniSTS	GRCh37
Build 36	21	39,702,905 - 39,703,141	RGD	NCBI36
Celera	21	25,978,729 - 25,978,965	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,249,881 - 26,250,117	UniSTS

REN20470

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,781,248 - 40,781,483	UniSTS	GRCh37
Build 36	21	39,703,118 - 39,703,353	RGD	NCBI36
Celera	21	25,978,942 - 25,979,177	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,250,094 - 26,250,329	UniSTS

REN20471

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,781,447 - 40,781,695	UniSTS	GRCh37
Build 36	21	39,703,317 - 39,703,565	RGD	NCBI36
Celera	21	25,979,141 - 25,979,389	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,250,293 - 26,250,541	UniSTS

REN20472

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,781,671 - 40,781,938	UniSTS	GRCh37
Build 36	21	39,703,541 - 39,703,808	RGD	NCBI36
Celera	21	25,979,365 - 25,979,632	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,250,517 - 26,250,784	UniSTS

REN20473

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,781,926 - 40,782,181	UniSTS	GRCh37
Build 36	21	39,703,796 - 39,704,051	RGD	NCBI36
Celera	21	25,979,620 - 25,979,875	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,250,772 - 26,251,027	UniSTS

REN20474

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,782,021 - 40,782,286	UniSTS	GRCh37
Build 36	21	39,703,891 - 39,704,156	RGD	NCBI36
Celera	21	25,979,715 - 25,979,980	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,250,867 - 26,251,132	UniSTS

REN20475

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,782,280 - 40,782,545	UniSTS	GRCh37
Build 36	21	39,704,150 - 39,704,415	RGD	NCBI36
Celera	21	25,979,974 - 25,980,239	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,251,126 - 26,251,391	UniSTS

REN20476

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,782,526 - 40,782,795	UniSTS	GRCh37
Build 36	21	39,704,396 - 39,704,665	RGD	NCBI36
Celera	21	25,980,220 - 25,980,489	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,251,372 - 26,251,641	UniSTS

REN20477

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,782,768 - 40,782,992	UniSTS	GRCh37
Build 36	21	39,704,638 - 39,704,862	RGD	NCBI36
Celera	21	25,980,462 - 25,980,686	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,251,614 - 26,251,838	UniSTS

REN20478

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,782,955 - 40,783,197	UniSTS	GRCh37
Build 36	21	39,704,825 - 39,705,067	RGD	NCBI36
Celera	21	25,980,649 - 25,980,891	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,251,801 - 26,252,043	UniSTS

REN20479

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,783,195 - 40,783,438	UniSTS	GRCh37
Build 36	21	39,705,065 - 39,705,308	RGD	NCBI36
Celera	21	25,980,889 - 25,981,132	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,252,041 - 26,252,284	UniSTS

REN20480

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,783,415 - 40,783,666	UniSTS	GRCh37
Build 36	21	39,705,285 - 39,705,536	RGD	NCBI36
Celera	21	25,981,109 - 25,981,360	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,252,261 - 26,252,512	UniSTS

REN20481

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,783,643 - 40,783,893	UniSTS	GRCh37
Build 36	21	39,705,513 - 39,705,763	RGD	NCBI36
Celera	21	25,981,337 - 25,981,587	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,252,489 - 26,252,739	UniSTS

REN20482

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,783,870 - 40,784,118	UniSTS	GRCh37
Build 36	21	39,705,740 - 39,705,988	RGD	NCBI36
Celera	21	25,981,564 - 25,981,812	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,252,716 - 26,252,964	UniSTS

REN20483

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,784,095 - 40,784,357	UniSTS	GRCh37
Build 36	21	39,705,965 - 39,706,227	RGD	NCBI36
Celera	21	25,981,789 - 25,982,051	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,252,941 - 26,253,203	UniSTS

REN20484

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,784,337 - 40,784,593	UniSTS	GRCh37
Build 36	21	39,706,207 - 39,706,463	RGD	NCBI36
Celera	21	25,982,031 - 25,982,287	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,253,183 - 26,253,439	UniSTS

REN20485

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,784,572 - 40,784,826	UniSTS	GRCh37
Build 36	21	39,706,442 - 39,706,696	RGD	NCBI36
Celera	21	25,982,266 - 25,982,520	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,253,418 - 26,253,672	UniSTS

REN20486

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,784,805 - 40,785,054	UniSTS	GRCh37
Build 36	21	39,706,675 - 39,706,924	RGD	NCBI36
Celera	21	25,982,499 - 25,982,748	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,253,651 - 26,253,900	UniSTS

REN20487

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,785,031 - 40,785,267	UniSTS	GRCh37
Build 36	21	39,706,901 - 39,707,137	RGD	NCBI36
Celera	21	25,982,725 - 25,982,961	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,253,877 - 26,254,113	UniSTS

REN20488

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,785,244 - 40,785,500	UniSTS	GRCh37
Build 36	21	39,707,114 - 39,707,370	RGD	NCBI36
Celera	21	25,982,938 - 25,983,194	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,254,090 - 26,254,346	UniSTS

REN20489

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,785,475 - 40,785,721	UniSTS	GRCh37
Build 36	21	39,707,345 - 39,707,591	RGD	NCBI36
Celera	21	25,983,169 - 25,983,415	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,254,321 - 26,254,567	UniSTS

REN20490

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,785,687 - 40,785,934	UniSTS	GRCh37
Build 36	21	39,707,557 - 39,707,804	RGD	NCBI36
Celera	21	25,983,381 - 25,983,628	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,254,533 - 26,254,780	UniSTS

REN20491

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,785,913 - 40,786,144	UniSTS	GRCh37
Build 36	21	39,707,783 - 39,708,014	RGD	NCBI36
Celera	21	25,983,607 - 25,983,838	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,254,759 - 26,254,990	UniSTS

REN20492

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,786,121 - 40,786,357	UniSTS	GRCh37
Build 36	21	39,707,991 - 39,708,227	RGD	NCBI36
Celera	21	25,983,815 - 25,984,051	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,254,967 - 26,255,203	UniSTS

REN20493

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,786,333 - 40,786,579	UniSTS	GRCh37
Build 36	21	39,708,203 - 39,708,449	RGD	NCBI36
Celera	21	25,984,027 - 25,984,273	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,255,179 - 26,255,425	UniSTS

REN20494

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,786,557 - 40,786,805	UniSTS	GRCh37
Build 36	21	39,708,427 - 39,708,675	RGD	NCBI36
Celera	21	25,984,251 - 25,984,499	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,255,403 - 26,255,657	UniSTS

REN20495

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,786,803 - 40,787,034	UniSTS	GRCh37
Build 36	21	39,708,673 - 39,708,904	RGD	NCBI36
Celera	21	25,984,497 - 25,984,728	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,255,655 - 26,255,886	UniSTS

REN20496

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,787,006 - 40,787,230	UniSTS	GRCh37
Build 36	21	39,708,876 - 39,709,100	RGD	NCBI36
Celera	21	25,984,700 - 25,984,924	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,255,858 - 26,256,082	UniSTS

REN20497

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,787,186 - 40,787,410	UniSTS	GRCh37
Build 36	21	39,709,056 - 39,709,280	RGD	NCBI36
Celera	21	25,984,880 - 25,985,104	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,256,038 - 26,256,262	UniSTS

REN20498

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,787,381 - 40,787,637	UniSTS	GRCh37
Build 36	21	39,709,251 - 39,709,507	RGD	NCBI36
Celera	21	25,985,075 - 25,985,331	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,256,233 - 26,256,489	UniSTS

REN20499

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,787,622 - 40,787,864	UniSTS	GRCh37
Build 36	21	39,709,492 - 39,709,734	RGD	NCBI36
Celera	21	25,985,316 - 25,985,558	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,256,474 - 26,256,716	UniSTS

REN20500

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,787,841 - 40,788,087	UniSTS	GRCh37
Build 36	21	39,709,711 - 39,709,957	RGD	NCBI36
Celera	21	25,985,535 - 25,985,781	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,256,693 - 26,256,939	UniSTS

REN20501

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,788,077 - 40,788,323	UniSTS	GRCh37
Build 36	21	39,709,947 - 39,710,193	RGD	NCBI36
Celera	21	25,985,771 - 25,986,017	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,256,929 - 26,257,175	UniSTS

REN20502

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,788,300 - 40,788,550	UniSTS	GRCh37
Build 36	21	39,710,170 - 39,710,420	RGD	NCBI36
Celera	21	25,985,994 - 25,986,244	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,257,152 - 26,257,402	UniSTS

REN20503

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,788,527 - 40,788,780	UniSTS	GRCh37
Build 36	21	39,710,397 - 39,710,650	RGD	NCBI36
Celera	21	25,986,221 - 25,986,474	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,257,379 - 26,257,632	UniSTS

REN20504

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,788,738 - 40,788,962	UniSTS	GRCh37
Build 36	21	39,710,608 - 39,710,832	RGD	NCBI36
Celera	21	25,986,432 - 25,986,656	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,257,590 - 26,257,814	UniSTS

REN20505

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,788,806 - 40,789,049	UniSTS	GRCh37
Build 36	21	39,710,676 - 39,710,919	RGD	NCBI36
Celera	21	25,986,500 - 25,986,743	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,257,658 - 26,257,901	UniSTS

REN20506

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,789,350 - 40,789,615	UniSTS	GRCh37
Build 36	21	39,711,220 - 39,711,485	RGD	NCBI36
Celera	21	25,987,044 - 25,987,309	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,258,202 - 26,258,467	UniSTS

REN20507

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,789,437 - 40,789,668	UniSTS	GRCh37
Build 36	21	39,711,307 - 39,711,538	RGD	NCBI36
Celera	21	25,987,131 - 25,987,362	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,258,289 - 26,258,520	UniSTS

REN20508

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,790,057 - 40,790,311	UniSTS	GRCh37
Build 36	21	39,711,927 - 39,712,181	RGD	NCBI36
Celera	21	25,987,751 - 25,988,005	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,258,909 - 26,259,163	UniSTS

REN20509

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,790,760 - 40,791,008	UniSTS	GRCh37
Build 36	21	39,712,630 - 39,712,878	RGD	NCBI36
Celera	21	25,988,454 - 25,988,702	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,259,612 - 26,259,860	UniSTS

REN20510

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,790,922 - 40,791,177	UniSTS	GRCh37
Build 36	21	39,712,792 - 39,713,047	RGD	NCBI36
Celera	21	25,988,616 - 25,988,871	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,259,774 - 26,260,029	UniSTS

REN20511

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,791,476 - 40,791,704	UniSTS	GRCh37
Build 36	21	39,713,346 - 39,713,574	RGD	NCBI36
Celera	21	25,989,171 - 25,989,399	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,260,329 - 26,260,557	UniSTS

REN20512

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,791,570 - 40,791,796	UniSTS	GRCh37
Build 36	21	39,713,440 - 39,713,666	RGD	NCBI36
Celera	21	25,989,265 - 25,989,491	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,260,423 - 26,260,649	UniSTS

REN20513

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,791,763 - 40,792,023	UniSTS	GRCh37
Build 36	21	39,713,633 - 39,713,893	RGD	NCBI36
Celera	21	25,989,458 - 25,989,718	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,260,616 - 26,260,876	UniSTS

REN20514

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,791,952 - 40,792,176	UniSTS	GRCh37
Build 36	21	39,713,822 - 39,714,046	RGD	NCBI36
Celera	21	25,989,647 - 25,989,871	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,260,805 - 26,261,029	UniSTS

REN20515

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,792,098 - 40,792,339	UniSTS	GRCh37
Build 36	21	39,713,968 - 39,714,209	RGD	NCBI36
Celera	21	25,989,793 - 25,990,034	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,260,951 - 26,261,192	UniSTS

REN20516

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,792,335 - 40,792,598	UniSTS	GRCh37
Build 36	21	39,714,205 - 39,714,468	RGD	NCBI36
Celera	21	25,990,030 - 25,990,294	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,261,188 - 26,261,458	UniSTS

REN20517

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,792,582 - 40,792,821	UniSTS	GRCh37
Build 36	21	39,714,452 - 39,714,691	RGD	NCBI36
Celera	21	25,990,278 - 25,990,517	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,261,442 - 26,261,681	UniSTS

REN20518

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,792,738 - 40,792,988	UniSTS	GRCh37
Build 36	21	39,714,608 - 39,714,858	RGD	NCBI36
Celera	21	25,990,434 - 25,990,684	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,261,598 - 26,261,848	UniSTS

REN20519

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,792,835 - 40,793,069	UniSTS	GRCh37
Build 36	21	39,714,705 - 39,714,939	RGD	NCBI36
Celera	21	25,990,531 - 25,990,765	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,261,695 - 26,261,929	UniSTS

REN20520

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,793,148 - 40,793,390	UniSTS	GRCh37
Build 36	21	39,715,018 - 39,715,260	RGD	NCBI36
Celera	21	25,990,844 - 25,991,086	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,262,008 - 26,262,250	UniSTS

REN20521

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,793,370 - 40,793,637	UniSTS	GRCh37
Build 36	21	39,715,240 - 39,715,507	RGD	NCBI36
Celera	21	25,991,066 - 25,991,333	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,262,230 - 26,262,497	UniSTS

REN20522

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,793,611 - 40,793,846	UniSTS	GRCh37
Build 36	21	39,715,481 - 39,715,716	RGD	NCBI36
Celera	21	25,991,307 - 25,991,542	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,262,471 - 26,262,706	UniSTS

REN20523

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,793,814 - 40,794,060	UniSTS	GRCh37
Build 36	21	39,715,684 - 39,715,930	RGD	NCBI36
Celera	21	25,991,510 - 25,991,756	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,262,674 - 26,262,920	UniSTS

REN20524

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,794,035 - 40,794,281	UniSTS	GRCh37
Build 36	21	39,715,905 - 39,716,151	RGD	NCBI36
Celera	21	25,991,731 - 25,991,977	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,262,895 - 26,263,138	UniSTS

REN20525

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,794,248 - 40,794,500	UniSTS	GRCh37
Build 36	21	39,716,118 - 39,716,370	RGD	NCBI36
Celera	21	25,991,944 - 25,992,196	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,263,105 - 26,263,357	UniSTS

REN20526

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,794,477 - 40,794,749	UniSTS	GRCh37
Build 36	21	39,716,347 - 39,716,619	RGD	NCBI36
Celera	21	25,992,173 - 25,992,445	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,263,334 - 26,263,606	UniSTS

REN20527

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,794,740 - 40,794,979	UniSTS	GRCh37
Build 36	21	39,716,610 - 39,716,849	RGD	NCBI36
Celera	21	25,992,436 - 25,992,675	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,263,597 - 26,263,836	UniSTS

REN20528

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,794,953 - 40,795,211	UniSTS	GRCh37
Build 36	21	39,716,823 - 39,717,081	RGD	NCBI36
Celera	21	25,992,649 - 25,992,907	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,263,810 - 26,264,068	UniSTS

REN20529

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,795,187 - 40,795,423	UniSTS	GRCh37
Build 36	21	39,717,057 - 39,717,293	RGD	NCBI36
Celera	21	25,992,883 - 25,993,119	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,264,044 - 26,264,280	UniSTS

REN20530

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,795,416 - 40,795,685	UniSTS	GRCh37
Build 36	21	39,717,286 - 39,717,555	RGD	NCBI36
Celera	21	25,993,112 - 25,993,381	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,264,273 - 26,264,542	UniSTS

REN20531

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,795,683 - 40,795,910	UniSTS	GRCh37
Build 36	21	39,717,553 - 39,717,780	RGD	NCBI36
Celera	21	25,993,379 - 25,993,606	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,264,540 - 26,264,767	UniSTS

REN20532

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,795,696 - 40,795,920	UniSTS	GRCh37
Build 36	21	39,717,566 - 39,717,790	RGD	NCBI36
Celera	21	25,993,392 - 25,993,616	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,264,553 - 26,264,777	UniSTS

REN20533

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,796,073 - 40,796,307	UniSTS	GRCh37
Build 36	21	39,717,943 - 39,718,177	RGD	NCBI36
Celera	21	25,993,769 - 25,994,003	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,264,930 - 26,265,164	UniSTS

REN20534

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,796,291 - 40,796,532	UniSTS	GRCh37
Build 36	21	39,718,161 - 39,718,402	RGD	NCBI36
Celera	21	25,993,987 - 25,994,228	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,265,148 - 26,265,389	UniSTS

REN20535

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,796,528 - 40,796,787	UniSTS	GRCh37
Build 36	21	39,718,398 - 39,718,657	RGD	NCBI36
Celera	21	25,994,224 - 25,994,483	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,265,385 - 26,265,644	UniSTS

REN20536

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,796,760 - 40,797,003	UniSTS	GRCh37
Build 36	21	39,718,630 - 39,718,873	RGD	NCBI36
Celera	21	25,994,456 - 25,994,699	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,265,617 - 26,265,860	UniSTS

REN20537

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,796,980 - 40,797,237	UniSTS	GRCh37
Build 36	21	39,718,850 - 39,719,107	RGD	NCBI36
Celera	21	25,994,676 - 25,994,933	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,265,837 - 26,266,094	UniSTS

REN20538

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,797,219 - 40,797,467	UniSTS	GRCh37
Build 36	21	39,719,089 - 39,719,337	RGD	NCBI36
Celera	21	25,994,915 - 25,995,163	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,266,076 - 26,266,324	UniSTS

REN20539

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,797,444 - 40,797,697	UniSTS	GRCh37
Build 36	21	39,719,314 - 39,719,567	RGD	NCBI36
Celera	21	25,995,140 - 25,995,393	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,266,301 - 26,266,554	UniSTS

REN20540

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,797,629 - 40,797,894	UniSTS	GRCh37
Build 36	21	39,719,499 - 39,719,764	RGD	NCBI36
Celera	21	25,995,325 - 25,995,590	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,266,486 - 26,266,751	UniSTS

REN20541

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,797,872 - 40,798,104	UniSTS	GRCh37
Build 36	21	39,719,742 - 39,719,974	RGD	NCBI36
Celera	21	25,995,568 - 25,995,800	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,266,729 - 26,266,961	UniSTS

REN20542

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,798,063 - 40,798,319	UniSTS	GRCh37
Build 36	21	39,719,933 - 39,720,189	RGD	NCBI36
Celera	21	25,995,759 - 25,996,015	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,266,920 - 26,267,176	UniSTS

REN20543

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,798,299 - 40,798,539	UniSTS	GRCh37
Build 36	21	39,720,169 - 39,720,409	RGD	NCBI36
Celera	21	25,995,995 - 25,996,235	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,267,156 - 26,267,396	UniSTS

REN20544

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,798,537 - 40,798,785	UniSTS	GRCh37
Build 36	21	39,720,407 - 39,720,655	RGD	NCBI36
Celera	21	25,996,233 - 25,996,481	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,267,394 - 26,267,642	UniSTS

REN20545

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,798,765 - 40,798,995	UniSTS	GRCh37
Build 36	21	39,720,635 - 39,720,865	RGD	NCBI36
Celera	21	25,996,461 - 25,996,691	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,267,622 - 26,267,852	UniSTS

REN20546

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,798,953 - 40,799,203	UniSTS	GRCh37
Build 36	21	39,720,823 - 39,721,073	RGD	NCBI36
Celera	21	25,996,649 - 25,996,899	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,267,810 - 26,268,060	UniSTS

REN20547

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,799,078 - 40,799,314	UniSTS	GRCh37
Build 36	21	39,720,948 - 39,721,184	RGD	NCBI36
Celera	21	25,996,774 - 25,997,010	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,267,935 - 26,268,171	UniSTS

REN20548

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,799,560 - 40,799,787	UniSTS	GRCh37
Build 36	21	39,721,430 - 39,721,657	RGD	NCBI36
Celera	21	25,997,256 - 25,997,483	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,268,417 - 26,268,644	UniSTS

REN20549

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,799,776 - 40,800,039	UniSTS	GRCh37
Build 36	21	39,721,646 - 39,721,909	RGD	NCBI36
Celera	21	25,997,472 - 25,997,735	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,268,633 - 26,268,896	UniSTS

REN20550

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,800,017 - 40,800,268	UniSTS	GRCh37
Build 36	21	39,721,887 - 39,722,138	RGD	NCBI36
Celera	21	25,997,713 - 25,997,964	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,268,874 - 26,269,125	UniSTS

REN20551

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,800,236 - 40,800,504	UniSTS	GRCh37
Build 36	21	39,722,106 - 39,722,374	RGD	NCBI36
Celera	21	25,997,932 - 25,998,200	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,269,093 - 26,269,361	UniSTS

REN20552

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,800,472 - 40,800,696	UniSTS	GRCh37
Build 36	21	39,722,342 - 39,722,566	RGD	NCBI36
Celera	21	25,998,168 - 25,998,392	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,269,329 - 26,269,575	UniSTS

REN20553

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,800,689 - 40,800,941	UniSTS	GRCh37
Build 36	21	39,722,559 - 39,722,811	RGD	NCBI36
Celera	21	25,998,385 - 25,998,637	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,269,568 - 26,269,820	UniSTS

REN20554

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,800,926 - 40,801,191	UniSTS	GRCh37
Build 36	21	39,722,796 - 39,723,061	RGD	NCBI36
Celera	21	25,998,622 - 25,998,887	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,269,805 - 26,270,070	UniSTS

REN20555

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,801,182 - 40,801,444	UniSTS	GRCh37
Build 36	21	39,723,052 - 39,723,314	RGD	NCBI36
Celera	21	25,998,878 - 25,999,140	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,270,061 - 26,270,323	UniSTS

REN20556

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,801,428 - 40,801,699	UniSTS	GRCh37
Build 36	21	39,723,298 - 39,723,569	RGD	NCBI36
Celera	21	25,999,124 - 25,999,395	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,270,307 - 26,270,578	UniSTS

REN20557

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,801,670 - 40,801,938	UniSTS	GRCh37
Build 36	21	39,723,540 - 39,723,808	RGD	NCBI36
Celera	21	25,999,366 - 25,999,634	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,270,549 - 26,270,817	UniSTS

REN20558

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,801,921 - 40,802,158	UniSTS	GRCh37
Build 36	21	39,723,791 - 39,724,028	RGD	NCBI36
Celera	21	25,999,617 - 25,999,854	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,270,800 - 26,271,037	UniSTS

REN20559

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,802,135 - 40,802,394	UniSTS	GRCh37
Build 36	21	39,724,005 - 39,724,264	RGD	NCBI36
Celera	21	25,999,831 - 26,000,090	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,271,014 - 26,271,273	UniSTS

REN20560

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,802,385 - 40,802,640	UniSTS	GRCh37
Build 36	21	39,724,255 - 39,724,510	RGD	NCBI36
Celera	21	26,000,081 - 26,000,336	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,271,264 - 26,271,519	UniSTS

REN20561

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,802,600 - 40,802,860	UniSTS	GRCh37
Build 36	21	39,724,470 - 39,724,730	RGD	NCBI36
Celera	21	26,000,296 - 26,000,556	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,271,479 - 26,271,739	UniSTS

REN20562

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,802,837 - 40,803,092	UniSTS	GRCh37
Build 36	21	39,724,707 - 39,724,962	RGD	NCBI36
Celera	21	26,000,533 - 26,000,788	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,271,716 - 26,271,971	UniSTS

REN20563

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,803,086 - 40,803,331	UniSTS	GRCh37
Build 36	21	39,724,956 - 39,725,201	RGD	NCBI36
Celera	21	26,000,782 - 26,001,027	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,271,965 - 26,272,210	UniSTS

REN20564

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,803,187 - 40,803,430	UniSTS	GRCh37
Build 36	21	39,725,057 - 39,725,300	RGD	NCBI36
Celera	21	26,000,883 - 26,001,126	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,272,066 - 26,272,309	UniSTS

REN20565

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,803,736 - 40,803,978	UniSTS	GRCh37
Build 36	21	39,725,606 - 39,725,848	RGD	NCBI36
Celera	21	26,001,432 - 26,001,674	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,272,615 - 26,272,857	UniSTS

REN20566

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,803,946 - 40,804,183	UniSTS	GRCh37
Build 36	21	39,725,816 - 39,726,053	RGD	NCBI36
Celera	21	26,001,642 - 26,001,879	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,272,825 - 26,273,062	UniSTS

REN20567

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,804,159 - 40,804,412	UniSTS	GRCh37
Build 36	21	39,726,029 - 39,726,282	RGD	NCBI36
Celera	21	26,001,855 - 26,002,108	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,273,038 - 26,273,291	UniSTS

REN20568

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,804,400 - 40,804,624	UniSTS	GRCh37
Build 36	21	39,726,270 - 39,726,494	RGD	NCBI36
Celera	21	26,002,096 - 26,002,320	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,273,279 - 26,273,503	UniSTS

REN20569

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,804,612 - 40,804,875	UniSTS	GRCh37
Build 36	21	39,726,482 - 39,726,745	RGD	NCBI36
Celera	21	26,002,308 - 26,002,571	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,273,491 - 26,273,754	UniSTS

REN20570

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,804,835 - 40,805,059	UniSTS	GRCh37
Build 36	21	39,726,705 - 39,726,929	RGD	NCBI36
Celera	21	26,002,531 - 26,002,755	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,273,714 - 26,273,938	UniSTS

REN20571

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,804,940 - 40,805,177	UniSTS	GRCh37
Build 36	21	39,726,810 - 39,727,047	RGD	NCBI36
Celera	21	26,002,636 - 26,002,873	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,273,819 - 26,274,056	UniSTS

REN20572

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,805,154 - 40,805,390	UniSTS	GRCh37
Build 36	21	39,727,024 - 39,727,260	RGD	NCBI36
Celera	21	26,002,850 - 26,003,086	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,274,033 - 26,274,269	UniSTS

REN20573

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,805,366 - 40,805,625	UniSTS	GRCh37
Build 36	21	39,727,236 - 39,727,495	RGD	NCBI36
Celera	21	26,003,062 - 26,003,321	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,274,245 - 26,274,504	UniSTS

REN20574

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,805,513 - 40,805,737	UniSTS	GRCh37
Build 36	21	39,727,383 - 39,727,607	RGD	NCBI36
Celera	21	26,003,209 - 26,003,433	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,274,392 - 26,274,616	UniSTS

REN20575

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,805,707 - 40,805,940	UniSTS	GRCh37
Build 36	21	39,727,577 - 39,727,810	RGD	NCBI36
Celera	21	26,003,403 - 26,003,635	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,274,586 - 26,274,818	UniSTS

REN20576

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,805,910 - 40,806,158	UniSTS	GRCh37
Build 36	21	39,727,780 - 39,728,028	RGD	NCBI36
Celera	21	26,003,605 - 26,003,853	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,274,788 - 26,275,036	UniSTS

REN20577

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,806,137 - 40,806,400	UniSTS	GRCh37
Build 36	21	39,728,007 - 39,728,270	RGD	NCBI36
Celera	21	26,003,832 - 26,004,095	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,275,015 - 26,275,278	UniSTS

REN20578

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,806,233 - 40,806,473	UniSTS	GRCh37
Build 36	21	39,728,103 - 39,728,343	RGD	NCBI36
Celera	21	26,003,928 - 26,004,168	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,275,111 - 26,275,351	UniSTS

REN20579

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,806,560 - 40,806,799	UniSTS	GRCh37
Build 36	21	39,728,430 - 39,728,669	RGD	NCBI36
Celera	21	26,004,255 - 26,004,494	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,275,438 - 26,275,677	UniSTS

REN20580

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,806,772 - 40,806,996	UniSTS	GRCh37
Build 36	21	39,728,642 - 39,728,866	RGD	NCBI36
Celera	21	26,004,467 - 26,004,691	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,275,650 - 26,275,874	UniSTS

REN20581

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,806,970 - 40,807,233	UniSTS	GRCh37
Build 36	21	39,728,840 - 39,729,103	RGD	NCBI36
Celera	21	26,004,665 - 26,004,928	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,275,848 - 26,276,111	UniSTS

REN20582

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,807,215 - 40,807,441	UniSTS	GRCh37
Build 36	21	39,729,085 - 39,729,311	RGD	NCBI36
Celera	21	26,004,910 - 26,005,136	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,276,093 - 26,276,319	UniSTS

REN20583

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,807,398 - 40,807,632	UniSTS	GRCh37
Build 36	21	39,729,268 - 39,729,502	RGD	NCBI36
Celera	21	26,005,093 - 26,005,327	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,276,276 - 26,276,510	UniSTS

REN20584

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,807,879 - 40,808,104	UniSTS	GRCh37
Build 36	21	39,729,749 - 39,729,974	RGD	NCBI36
Celera	21	26,005,574 - 26,005,799	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,276,757 - 26,276,982	UniSTS

REN20585

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,808,018 - 40,808,242	UniSTS	GRCh37
Build 36	21	39,729,888 - 39,730,112	RGD	NCBI36
Celera	21	26,005,713 - 26,005,937	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,276,896 - 26,277,120	UniSTS

REN20586

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,808,163 - 40,808,389	UniSTS	GRCh37
Build 36	21	39,730,033 - 39,730,259	RGD	NCBI36
Celera	21	26,005,858 - 26,006,084	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,277,041 - 26,277,267	UniSTS

REN20587

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,808,364 - 40,808,614	UniSTS	GRCh37
Build 36	21	39,730,234 - 39,730,484	RGD	NCBI36
Celera	21	26,006,059 - 26,006,309	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,277,242 - 26,277,492	UniSTS

REN20588

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,808,586 - 40,808,817	UniSTS	GRCh37
Build 36	21	39,730,456 - 39,730,687	RGD	NCBI36
Celera	21	26,006,281 - 26,006,512	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,277,464 - 26,277,695	UniSTS

REN20589

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,808,794 - 40,809,057	UniSTS	GRCh37
Build 36	21	39,730,664 - 39,730,927	RGD	NCBI36
Celera	21	26,006,489 - 26,006,752	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,277,672 - 26,277,935	UniSTS

REN20590

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,809,030 - 40,809,292	UniSTS	GRCh37
Build 36	21	39,730,900 - 39,731,162	RGD	NCBI36
Celera	21	26,006,725 - 26,006,987	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,277,908 - 26,278,170	UniSTS

REN20591

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,809,120 - 40,809,383	UniSTS	GRCh37
Build 36	21	39,730,990 - 39,731,253	RGD	NCBI36
Celera	21	26,006,815 - 26,007,078	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,277,998 - 26,278,261	UniSTS

REN20592

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,809,648 - 40,809,901	UniSTS	GRCh37
Build 36	21	39,731,518 - 39,731,771	RGD	NCBI36
Celera	21	26,007,343 - 26,007,596	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,278,526 - 26,278,779	UniSTS

REN20593

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,809,863 - 40,810,092	UniSTS	GRCh37
Build 36	21	39,731,733 - 39,731,962	RGD	NCBI36
Celera	21	26,007,558 - 26,007,787	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,278,741 - 26,278,970	UniSTS

REN20594

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,810,066 - 40,810,290	UniSTS	GRCh37
Build 36	21	39,731,936 - 39,732,160	RGD	NCBI36
Celera	21	26,007,761 - 26,007,985	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,278,944 - 26,279,168	UniSTS

REN20595

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,810,260 - 40,810,501	UniSTS	GRCh37
Build 36	21	39,732,130 - 39,732,371	RGD	NCBI36
Celera	21	26,007,955 - 26,008,196	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,279,138 - 26,279,379	UniSTS

REN20596

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,810,419 - 40,810,661	UniSTS	GRCh37
Build 36	21	39,732,289 - 39,732,531	RGD	NCBI36
Celera	21	26,008,114 - 26,008,356	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,279,297 - 26,279,539	UniSTS

REN20597

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,810,638 - 40,810,893	UniSTS	GRCh37
Build 36	21	39,732,508 - 39,732,763	RGD	NCBI36
Celera	21	26,008,333 - 26,008,588	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,279,516 - 26,279,771	UniSTS

REN20598

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,810,869 - 40,811,111	UniSTS	GRCh37
Build 36	21	39,732,739 - 39,732,981	RGD	NCBI36
Celera	21	26,008,564 - 26,008,806	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,279,747 - 26,279,989	UniSTS

REN20599

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,811,088 - 40,811,328	UniSTS	GRCh37
Build 36	21	39,732,958 - 39,733,198	RGD	NCBI36
Celera	21	26,008,783 - 26,009,023	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,279,966 - 26,280,206	UniSTS

REN20600

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,811,236 - 40,811,493	UniSTS	GRCh37
Build 36	21	39,733,106 - 39,733,363	RGD	NCBI36
Celera	21	26,008,931 - 26,009,188	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,280,114 - 26,280,371	UniSTS

REN20601

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,811,481 - 40,811,731	UniSTS	GRCh37
Build 36	21	39,733,351 - 39,733,601	RGD	NCBI36
Celera	21	26,009,176 - 26,009,426	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,280,359 - 26,280,609	UniSTS

REN20602

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,811,729 - 40,811,957	UniSTS	GRCh37
Build 36	21	39,733,599 - 39,733,827	RGD	NCBI36
Celera	21	26,009,424 - 26,009,652	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,280,607 - 26,280,835	UniSTS

REN20603

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,811,928 - 40,812,172	UniSTS	GRCh37
Build 36	21	39,733,798 - 39,734,042	RGD	NCBI36
Celera	21	26,009,623 - 26,009,867	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,280,806 - 26,281,050	UniSTS

REN20604

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,812,039 - 40,812,296	UniSTS	GRCh37
Build 36	21	39,733,909 - 39,734,166	RGD	NCBI36
Celera	21	26,009,734 - 26,009,991	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,280,917 - 26,281,174	UniSTS

REN20605

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,812,277 - 40,812,533	UniSTS	GRCh37
Build 36	21	39,734,147 - 39,734,403	RGD	NCBI36
Celera	21	26,009,972 - 26,010,228	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,281,155 - 26,281,411	UniSTS

REN20606

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,812,510 - 40,812,752	UniSTS	GRCh37
Build 36	21	39,734,380 - 39,734,622	RGD	NCBI36
Celera	21	26,010,205 - 26,010,447	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,281,388 - 26,281,630	UniSTS

REN20607

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,812,728 - 40,812,986	UniSTS	GRCh37
Build 36	21	39,734,598 - 39,734,856	RGD	NCBI36
Celera	21	26,010,423 - 26,010,681	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,281,606 - 26,281,864	UniSTS

REN20608

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,812,943 - 40,813,210	UniSTS	GRCh37
Build 36	21	39,734,813 - 39,735,080	RGD	NCBI36
Celera	21	26,010,638 - 26,010,905	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,281,821 - 26,282,088	UniSTS

REN20609

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,813,194 - 40,813,460	UniSTS	GRCh37
Build 36	21	39,735,064 - 39,735,330	RGD	NCBI36
Celera	21	26,010,889 - 26,011,155	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,282,072 - 26,282,338	UniSTS

REN20610

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,813,458 - 40,813,688	UniSTS	GRCh37
Build 36	21	39,735,328 - 39,735,558	RGD	NCBI36
Celera	21	26,011,153 - 26,011,383	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,282,336 - 26,282,566	UniSTS

REN20611

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,813,647 - 40,813,898	UniSTS	GRCh37
Build 36	21	39,735,517 - 39,735,768	RGD	NCBI36
Celera	21	26,011,342 - 26,011,593	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,282,525 - 26,282,776	UniSTS

REN20612

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,813,883 - 40,814,126	UniSTS	GRCh37
Build 36	21	39,735,753 - 39,735,996	RGD	NCBI36
Celera	21	26,011,578 - 26,011,821	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,282,761 - 26,283,004	UniSTS

REN20613

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,814,079 - 40,814,345	UniSTS	GRCh37
Build 36	21	39,735,949 - 39,736,215	RGD	NCBI36
Celera	21	26,011,774 - 26,012,040	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,282,957 - 26,283,223	UniSTS

REN20614

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,814,317 - 40,814,560	UniSTS	GRCh37
Build 36	21	39,736,187 - 39,736,430	RGD	NCBI36
Celera	21	26,012,012 - 26,012,255	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,283,195 - 26,283,438	UniSTS

REN20615

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,814,545 - 40,814,771	UniSTS	GRCh37
Build 36	21	39,736,415 - 39,736,641	RGD	NCBI36
Celera	21	26,012,240 - 26,012,466	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,283,423 - 26,283,649	UniSTS

REN20616

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,814,735 - 40,814,987	UniSTS	GRCh37
Build 36	21	39,736,605 - 39,736,857	RGD	NCBI36
Celera	21	26,012,430 - 26,012,682	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,283,613 - 26,283,865	UniSTS

REN20617

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,814,957 - 40,815,197	UniSTS	GRCh37
Build 36	21	39,736,827 - 39,737,067	RGD	NCBI36
Celera	21	26,012,652 - 26,012,892	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,283,835 - 26,284,075	UniSTS

REN20618

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,815,163 - 40,815,411	UniSTS	GRCh37
Build 36	21	39,737,033 - 39,737,281	RGD	NCBI36
Celera	21	26,012,858 - 26,013,106	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,284,041 - 26,284,289	UniSTS

REN20619

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,815,395 - 40,815,644	UniSTS	GRCh37
Build 36	21	39,737,265 - 39,737,514	RGD	NCBI36
Celera	21	26,013,090 - 26,013,339	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,284,273 - 26,284,522	UniSTS

REN20620

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,815,432 - 40,815,678	UniSTS	GRCh37
Build 36	21	39,737,302 - 39,737,548	RGD	NCBI36
Celera	21	26,013,127 - 26,013,373	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,284,310 - 26,284,556	UniSTS

REN20621

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,815,644 - 40,815,893	UniSTS	GRCh37
Build 36	21	39,737,514 - 39,737,763	RGD	NCBI36
Celera	21	26,013,339 - 26,013,588	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,284,522 - 26,284,771	UniSTS

REN20622

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,815,868 - 40,816,118	UniSTS	GRCh37
Build 36	21	39,737,738 - 39,737,988	RGD	NCBI36
Celera	21	26,013,563 - 26,013,813	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,284,746 - 26,284,996	UniSTS

REN20623

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,816,078 - 40,816,336	UniSTS	GRCh37
Build 36	21	39,737,948 - 39,738,206	RGD	NCBI36
Celera	21	26,013,773 - 26,014,031	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,284,956 - 26,285,214	UniSTS

REN20624

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,816,335 - 40,816,575	UniSTS	GRCh37
Build 36	21	39,738,205 - 39,738,445	RGD	NCBI36
Celera	21	26,014,030 - 26,014,270	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,285,213 - 26,285,453	UniSTS

REN20625

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,816,531 - 40,816,776	UniSTS	GRCh37
Build 36	21	39,738,401 - 39,738,646	RGD	NCBI36
Celera	21	26,014,226 - 26,014,471	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,285,409 - 26,285,654	UniSTS

REN20626

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,816,753 - 40,817,019	UniSTS	GRCh37
Build 36	21	39,738,623 - 39,738,889	RGD	NCBI36
Celera	21	26,014,448 - 26,014,714	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,285,631 - 26,285,897	UniSTS

REN20627

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,816,997 - 40,817,248	UniSTS	GRCh37
Build 36	21	39,738,867 - 39,739,118	RGD	NCBI36
Celera	21	26,014,692 - 26,014,946	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,285,875 - 26,286,126	UniSTS

REN20628

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,817,225 - 40,817,477	UniSTS	GRCh37
Build 36	21	39,739,095 - 39,739,347	RGD	NCBI36
Celera	21	26,014,923 - 26,015,175	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,286,103 - 26,286,355	UniSTS

REN20629

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,817,404 - 40,817,664	UniSTS	GRCh37
Build 36	21	39,739,274 - 39,739,534	RGD	NCBI36
Celera	21	26,015,102 - 26,015,362	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,286,282 - 26,286,542	UniSTS

REN20630

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,817,646 - 40,817,896	UniSTS	GRCh37
Build 36	21	39,739,516 - 39,739,766	RGD	NCBI36
Celera	21	26,015,344 - 26,015,594	RGD
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
HuRef	21	26,286,524 - 26,286,774	UniSTS

G34554

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,798,972 - 40,799,131	UniSTS	GRCh37
Build 36	21	39,720,842 - 39,721,001	RGD	NCBI36
Celera	21	25,996,668 - 25,996,827	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,267,829 - 26,267,988	UniSTS

stSG622756

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,777,752 - 40,778,753	UniSTS	GRCh37
Build 36	21	39,699,622 - 39,700,623	RGD	NCBI36
Celera	21	25,975,446 - 25,976,447	RGD
HuRef	21	26,246,598 - 26,247,599	UniSTS

stSG622757

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,778,739 - 40,779,937	UniSTS	GRCh37
Build 36	21	39,700,609 - 39,701,807	RGD	NCBI36
Celera	21	25,976,433 - 25,977,631	RGD
HuRef	21	26,247,585 - 26,248,783	UniSTS

stSG622758

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,779,918 - 40,781,363	UniSTS	GRCh37
Build 36	21	39,701,788 - 39,703,233	RGD	NCBI36
Celera	21	25,977,612 - 25,979,057	RGD
HuRef	21	26,248,764 - 26,250,209	UniSTS

stSG622759

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,781,352 - 40,782,809	UniSTS	GRCh37
Build 36	21	39,703,222 - 39,704,679	RGD	NCBI36
Celera	21	25,979,046 - 25,980,503	RGD
HuRef	21	26,250,198 - 26,251,655	UniSTS

stSG622760

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,782,808 - 40,783,964	UniSTS	GRCh37
Build 36	21	39,704,678 - 39,705,834	RGD	NCBI36
Celera	21	25,980,502 - 25,981,658	RGD
HuRef	21	26,251,654 - 26,252,810	UniSTS

stSG622761

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,783,945 - 40,785,081	UniSTS	GRCh37
Build 36	21	39,705,815 - 39,706,951	RGD	NCBI36
Celera	21	25,981,639 - 25,982,775	RGD
HuRef	21	26,252,791 - 26,253,927	UniSTS

stSG622762

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,785,062 - 40,786,344	UniSTS	GRCh37
Build 36	21	39,706,932 - 39,708,214	RGD	NCBI36
Celera	21	25,982,756 - 25,984,038	RGD
HuRef	21	26,253,908 - 26,255,190	UniSTS

stSG622763

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,786,208 - 40,787,211	UniSTS	GRCh37
Build 36	21	39,708,078 - 39,709,081	RGD	NCBI36
Celera	21	25,983,902 - 25,984,905	RGD
HuRef	21	26,255,054 - 26,256,063	UniSTS

stSG622764

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,787,193 - 40,788,612	UniSTS	GRCh37
Build 36	21	39,709,063 - 39,710,482	RGD	NCBI36
Celera	21	25,984,887 - 25,986,306	RGD
HuRef	21	26,256,045 - 26,257,464	UniSTS

stSG622765

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,788,594 - 40,788,838	UniSTS	GRCh37
Build 36	21	39,710,464 - 39,710,708	RGD	NCBI36
Celera	21	25,986,288 - 25,986,532	RGD
HuRef	21	26,257,446 - 26,257,690	UniSTS

stSG622766

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,790,825 - 40,792,021	UniSTS	GRCh37
Build 36	21	39,712,695 - 39,713,891	RGD	NCBI36
Celera	21	25,988,519 - 25,989,716	RGD
HuRef	21	26,259,677 - 26,260,874	UniSTS

stSG622767

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,792,062 - 40,793,370	UniSTS	GRCh37
Build 36	21	39,713,932 - 39,715,240	RGD	NCBI36
Celera	21	25,989,757 - 25,991,066	RGD
HuRef	21	26,260,915 - 26,262,230	UniSTS

stSG622768

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,793,351 - 40,794,672	UniSTS	GRCh37
Build 36	21	39,715,221 - 39,716,542	RGD	NCBI36
Celera	21	25,991,047 - 25,992,368	RGD
HuRef	21	26,262,211 - 26,263,529	UniSTS

stSG622769

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,794,586 - 40,795,593	UniSTS	GRCh37
Build 36	21	39,716,456 - 39,717,463	RGD	NCBI36
Celera	21	25,992,282 - 25,993,289	RGD
Cytogenetic Map	21	q22.2	UniSTS
HuRef	21	26,263,443 - 26,264,450	UniSTS

stSG622770

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,795,573 - 40,796,940	UniSTS	GRCh37
Build 36	21	39,717,443 - 39,718,810	RGD	NCBI36
Celera	21	25,993,269 - 25,994,636	RGD
HuRef	21	26,264,430 - 26,265,797	UniSTS

stSG622772

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,798,714 - 40,799,785	UniSTS	GRCh37
Build 36	21	39,720,584 - 39,721,655	RGD	NCBI36
Celera	21	25,996,410 - 25,997,481	RGD
HuRef	21	26,267,571 - 26,268,642	UniSTS

stSG622773

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,799,772 - 40,801,262	UniSTS	GRCh37
Build 36	21	39,721,642 - 39,723,132	RGD	NCBI36
Celera	21	25,997,468 - 25,998,958	RGD
HuRef	21	26,268,629 - 26,270,141	UniSTS

stSG622774

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,801,413 - 40,802,496	UniSTS	GRCh37
Build 36	21	39,723,283 - 39,724,366	RGD	NCBI36
Celera	21	25,999,109 - 26,000,192	RGD
HuRef	21	26,270,292 - 26,271,375	UniSTS

stSG622775

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,802,479 - 40,803,912	UniSTS	GRCh37
Build 36	21	39,724,349 - 39,725,782	RGD	NCBI36
Celera	21	26,000,175 - 26,001,608	RGD
HuRef	21	26,271,358 - 26,272,791	UniSTS

stSG622776

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,803,404 - 40,804,415	UniSTS	GRCh37
Build 36	21	39,725,274 - 39,726,285	RGD	NCBI36
Celera	21	26,001,100 - 26,002,111	RGD
HuRef	21	26,272,283 - 26,273,294	UniSTS

stSG622777

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,805,904 - 40,807,060	UniSTS	GRCh37
Build 36	21	39,727,774 - 39,728,930	RGD	NCBI36
Celera	21	26,003,599 - 26,004,755	RGD
HuRef	21	26,274,782 - 26,275,938	UniSTS

stSG622778

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,807,051 - 40,808,132	UniSTS	GRCh37
Build 36	21	39,728,921 - 39,730,002	RGD	NCBI36
Celera	21	26,004,746 - 26,005,827	RGD
HuRef	21	26,275,929 - 26,277,010	UniSTS

stSG622779

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,808,116 - 40,809,115	UniSTS	GRCh37
Build 36	21	39,729,986 - 39,730,985	RGD	NCBI36
Celera	21	26,005,811 - 26,006,810	RGD
HuRef	21	26,276,994 - 26,277,993	UniSTS

stSG622780

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,809,096 - 40,810,280	UniSTS	GRCh37
Build 36	21	39,730,966 - 39,732,150	RGD	NCBI36
Celera	21	26,006,791 - 26,007,975	RGD
HuRef	21	26,277,974 - 26,279,158	UniSTS

stSG622781

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,810,261 - 40,811,520	UniSTS	GRCh37
Build 36	21	39,732,131 - 39,733,390	RGD	NCBI36
Celera	21	26,007,956 - 26,009,215	RGD
HuRef	21	26,279,139 - 26,280,398	UniSTS

stSG622782

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,811,515 - 40,812,932	UniSTS	GRCh37
Build 36	21	39,733,385 - 39,734,802	RGD	NCBI36
Celera	21	26,009,210 - 26,010,627	RGD
HuRef	21	26,280,393 - 26,281,810	UniSTS

stSG622783

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,812,911 - 40,813,276	UniSTS	GRCh37
Build 36	21	39,734,781 - 39,735,146	RGD	NCBI36
Celera	21	26,010,606 - 26,010,971	RGD
HuRef	21	26,281,789 - 26,282,154	UniSTS

stSG622784

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,813,296 - 40,813,582	UniSTS	GRCh37
Build 36	21	39,735,166 - 39,735,452	RGD	NCBI36
Celera	21	26,010,991 - 26,011,277	RGD
HuRef	21	26,282,174 - 26,282,460	UniSTS

stSG622785

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,813,563 - 40,813,807	UniSTS	GRCh37
Build 36	21	39,735,433 - 39,735,677	RGD	NCBI36
Celera	21	26,011,258 - 26,011,502	RGD
HuRef	21	26,282,441 - 26,282,685	UniSTS

stSG622786

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	21	40,815,573 - 40,817,028	UniSTS	GRCh37
Build 36	21	39,737,443 - 39,738,898	RGD	NCBI36
Celera	21	26,013,268 - 26,014,723	RGD
HuRef	21	26,284,451 - 26,285,906	UniSTS

D8S2278

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	5	p15.33	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	4	q32.1	UniSTS
Cytogenetic Map	6	q22	UniSTS
Cytogenetic Map	15	q15	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	16	q13	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	13	q14.3	UniSTS
Cytogenetic Map	12	q21.33	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	6	q25.3	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	3	p25.3-p24.1	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	2	q11.2-q12.1	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	10	q11	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	12	q21.31	UniSTS
Cytogenetic Map	2	q33-q34	UniSTS
Cytogenetic Map	22	q12.1	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	7	q34-q35	UniSTS
Cytogenetic Map	X	p22.1	UniSTS
Cytogenetic Map	1	q23.1	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	16	q24.3	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	2	q37	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	20	q13.31	UniSTS
Cytogenetic Map	6	p21.33	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	2	q37.1	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	12	p13.31	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	4	q34.1	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	6	q25	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	6	p22	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	8	q24	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	2	p23.1	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	12	p12.3	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	15	q22.1	UniSTS
Cytogenetic Map	1	p34-p33	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	17	q21.1	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	2	q12.3	UniSTS
Cytogenetic Map	3	q25.31	UniSTS
Cytogenetic Map	14	q22	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	12	p13.3	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	12	q21.1	UniSTS
Cytogenetic Map	X	p11.23	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	3	q26.32	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	13	q11	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	14	q12-q13	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	17	q11.2-q12	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	11	p15	UniSTS
Cytogenetic Map	4	q31	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	7	p22	UniSTS
Cytogenetic Map	15	q15-q21.1	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	10	q25.3	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	10	q24.32	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	6	q27	UniSTS
Cytogenetic Map	11	p15.3	UniSTS
Cytogenetic Map	4	q22.1-q23	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	17	q22-q23.2	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	18	q22.3	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	6	q22.31	UniSTS
Cytogenetic Map	1	p34.1	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	X	q26.1	UniSTS
Cytogenetic Map	4	q21.21	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	X	q13.2	UniSTS
Cytogenetic Map	2	q32.1	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.32	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	3	q27.3	UniSTS
Cytogenetic Map	10	p11.23	UniSTS
Cytogenetic Map	14	q32.11	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	X	p22.2	UniSTS
Cytogenetic Map	11	q14	UniSTS
Cytogenetic Map	13	q33.1	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	1	p31.3	UniSTS
Cytogenetic Map	1	q31-q41	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	14	q23	UniSTS
Cytogenetic Map	2	q24.2	UniSTS
Cytogenetic Map	7	q31	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	11	q12.2	UniSTS
Cytogenetic Map	14	q24.2	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	20	q11.22-q11.23	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	6	p24.3	UniSTS
Cytogenetic Map	9	p24.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	9	p21	UniSTS
Cytogenetic Map	6	p12.3	UniSTS
Cytogenetic Map	3	p12.1	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	17	q24.1	UniSTS
Cytogenetic Map	15	q13.1	UniSTS
Cytogenetic Map	12	q14.3-q15	UniSTS
Cytogenetic Map	15	q11-q13	UniSTS
Cytogenetic Map	12	q15	UniSTS
Cytogenetic Map	3	q28	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	2	p14	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	1	q44	UniSTS
Cytogenetic Map	14	q32.2	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	13	q32.2	UniSTS
Cytogenetic Map	2	q23.3	UniSTS
Cytogenetic Map	7	p21.1	UniSTS
Cytogenetic Map	8	p12-p11	UniSTS
Cytogenetic Map	1	q25	UniSTS
Cytogenetic Map	3	p21.32	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	10	q24	UniSTS
Cytogenetic Map	15	q13.3	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	13	q32.3	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	12	q24.33	UniSTS
Cytogenetic Map	5	q31.3	UniSTS
Cytogenetic Map	3	q13.2	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	5	q21.2	UniSTS
Cytogenetic Map	5	q15	UniSTS
Cytogenetic Map	3	p26.1	UniSTS
Cytogenetic Map	19	p13.13	UniSTS
Cytogenetic Map	19	q13.13	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	3	p22-p21.3	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	20	p11	UniSTS
Cytogenetic Map	2	p12	UniSTS
Cytogenetic Map	7	q21.13	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	5	q33.1	UniSTS
Cytogenetic Map	3	p21.1-p14.3	UniSTS
Cytogenetic Map	6	p12.1	UniSTS
Cytogenetic Map	7	q36.1	UniSTS
Cytogenetic Map	1	q32.3	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	6	q16.1	UniSTS
Cytogenetic Map	5	p13.1	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	9	q33.1	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	7	q35	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	2	p25.3	UniSTS
Cytogenetic Map	1	q22-q23	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	3	p26	UniSTS
Cytogenetic Map	4	q32.3	UniSTS
Cytogenetic Map	3	p14.2	UniSTS
Cytogenetic Map	18	q12.1	UniSTS
Cytogenetic Map	1	p36.3-p36.2	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	13	q14.11	UniSTS
Cytogenetic Map	12	p11.21	UniSTS
Cytogenetic Map	8	p21.1	UniSTS
Cytogenetic Map	7	p12.3	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	21	q21.1	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	20	p12.1	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	5	p13.2	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	16	q23.1	UniSTS
Cytogenetic Map	12	q23.3	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	1	p22.2	UniSTS
Cytogenetic Map	8	q23.3	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	2	q12	UniSTS
Cytogenetic Map	11	q25	UniSTS
Cytogenetic Map	X	p21.1	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	6	p21.31	UniSTS
Cytogenetic Map	5	p15.3	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	10	q21-q22	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	17	q24	UniSTS
Cytogenetic Map	1	p33-p32	UniSTS
Cytogenetic Map	7	p13-p11.1	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	7	q31.3	UniSTS
Cytogenetic Map	X	p22.13	UniSTS
Cytogenetic Map	14	q24	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	1	p13-p12	UniSTS
Cytogenetic Map	4	q32	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	10	q21.1	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	7	p14.1	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	7	q21.11	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	1	q12	UniSTS
Cytogenetic Map	3	q13.1-q13.2	UniSTS
Cytogenetic Map	11	p13	UniSTS
Cytogenetic Map	14	q32.3	UniSTS
Cytogenetic Map	14	q23.3	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	1	q24	UniSTS
Cytogenetic Map	1	q43	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	14	q22.3	UniSTS
Cytogenetic Map	14	q31	UniSTS

D11S2921

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	1	p36.1	UniSTS
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	7	p14.1	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	15	q13.2	UniSTS
Cytogenetic Map	16	q24.3	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	19	q13.11	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	14	q13.2	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	10	q24.33	UniSTS
Cytogenetic Map	5	q23.3-q31.1	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	17	q11	UniSTS
Cytogenetic Map	1	q24	UniSTS
Cytogenetic Map	11	q14	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	X	q13.1	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	2	q32.3	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	4	q32.1	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	13	q12	UniSTS
Cytogenetic Map	12	p13.31	UniSTS
Cytogenetic Map	3	p21.1	UniSTS
Cytogenetic Map	3	q12.3	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	6	q22	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	20	q11	UniSTS
Cytogenetic Map	8	q22.1	UniSTS
Cytogenetic Map	5	q23.3	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	11	q25	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	1	q32.3	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	12	q21.33	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	X	p11.4-p11.3	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	1	q24.1	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	10	p15.1	UniSTS
Cytogenetic Map	18	p11.31	UniSTS
Cytogenetic Map	12	p13.32	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	11	q13.5	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	2	q14	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	7	p22	UniSTS
Cytogenetic Map	14	q32.33	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	8	q24.11	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	9	q22.31	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	2	q33-q34	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	8	q24.13	UniSTS
Cytogenetic Map	22	q11.2	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	Y	p11.2	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	2	q37	UniSTS
Cytogenetic Map	18	pter-p11.3	UniSTS
Cytogenetic Map	8	q22.3	UniSTS
Cytogenetic Map	6	p21.33	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	2	q21.3	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	X	q22.1	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	14	q32.12	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	4	q34.1	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	3	q13.31	UniSTS
Cytogenetic Map	7	q21.12	UniSTS
Cytogenetic Map	15	q22.2	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	12	q23.2	UniSTS
Cytogenetic Map	6	p22	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	11	p13	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	16	p13.13	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	12	q13	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	1	q44	UniSTS
Cytogenetic Map	19	p13.1-p12	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	8	q24	UniSTS
Cytogenetic Map	18	p11.31-p11.21	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	7	p21.2	UniSTS
Cytogenetic Map	12	q23-q24.1	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	5	p15.33	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	1	q42.1	UniSTS
Cytogenetic Map	12	p13	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	2	q12.3	UniSTS
Cytogenetic Map	19	q13.3-q13.4	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	5	q35	UniSTS
Cytogenetic Map	8	p23-p22	UniSTS
Cytogenetic Map	12	p11	UniSTS
Cytogenetic Map	17	q21-q22	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	11	p13-p12	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	2	q12.1	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	3	q26.32	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	10	q11.22	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	5	q12-q13	UniSTS
Cytogenetic Map	6	p23	UniSTS
Cytogenetic Map	20	p12.3-p11.21	UniSTS
Cytogenetic Map	17	q11.2-q12	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	10	q23-q24	UniSTS
Cytogenetic Map	14	q21.3	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	12	q13-q14	UniSTS
Cytogenetic Map	6	q14.1	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	X	p22.2	UniSTS
Cytogenetic Map	1	p31	UniSTS
Cytogenetic Map	15	q15-q21.1	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	7	q21-q22	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	2	q33.3	UniSTS
Cytogenetic Map	11	q22.1	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	21	p11.1	UniSTS
Cytogenetic Map	14	q23.2	UniSTS
Cytogenetic Map	6	p22.3-p22.1	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	6	q15	UniSTS
Cytogenetic Map	X	q25-q26.3	UniSTS
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	12	q24.31-q24.32	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	9	q33.2	UniSTS
Cytogenetic Map	15	q23	UniSTS
Cytogenetic Map	12	p12.2-p11.2	UniSTS
Cytogenetic Map	2	q14.3	UniSTS
Cytogenetic Map	X	p11	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	20	q13.2	UniSTS
Cytogenetic Map	10	q26	UniSTS
Cytogenetic Map	6	q22.31	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	22	q13	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	18	p11.32	UniSTS
Cytogenetic Map	12	q15	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	2	p25.3	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	3	q27.3	UniSTS
Cytogenetic Map	4	p13	UniSTS
Cytogenetic Map	16	p12.1	UniSTS
Cytogenetic Map	14	q32.11	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	16	q12.1	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	20	q13.1	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	10	q23.33	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	9	p24.1-p23	UniSTS
Cytogenetic Map	15	q22	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	X	q12-q13	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	14	q23	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	1	q42.1-q43	UniSTS
Cytogenetic Map	7	q31.1-q31.3	UniSTS
Cytogenetic Map	20	q11.21	UniSTS
Cytogenetic Map	20	q12-q13.12	UniSTS
Cytogenetic Map	1	q24-q25.3	UniSTS
Cytogenetic Map	20	p12.1	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	6	q25.1-q26	UniSTS
Cytogenetic Map	12	q13.11-q14.3	UniSTS
Cytogenetic Map	7	p11	UniSTS
Cytogenetic Map	12	p11.22	UniSTS
Cytogenetic Map	17	q23.1	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	9	p11	UniSTS
Cytogenetic Map	6	p24.3	UniSTS
Cytogenetic Map	9	p24.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	6	p22.2	UniSTS
Cytogenetic Map	12	q24.2-q24.31	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	11	p11.11	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	11	q14.1	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	15	q22-q23	UniSTS
Cytogenetic Map	9	p21	UniSTS
Cytogenetic Map	15	q13.1	UniSTS
Cytogenetic Map	15	q22-qter	UniSTS
Cytogenetic Map	10	q25	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	5	p15.1	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	22	q13.31	UniSTS
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	13	q34	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	17	q24.3	UniSTS
Cytogenetic Map	16	q11.2	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	2	q23.3	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	18	q23	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	7	p21.1	UniSTS
Cytogenetic Map	2	q37.1	UniSTS
Cytogenetic Map	8	p11.2	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	2	q21.2	UniSTS
Cytogenetic Map	15	q13.3	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	3	p22.2	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	19	p13.2-cen	UniSTS
Cytogenetic Map	19	p13.3-p13.2	UniSTS
Cytogenetic Map	13	q32.3	UniSTS
Cytogenetic Map	9	q33	UniSTS
Cytogenetic Map	1	p36-p35	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	12	q23	UniSTS
Cytogenetic Map	21	q22.13	UniSTS
Cytogenetic Map	2	q24.2	UniSTS
Cytogenetic Map	7	q31.1-q31.2	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	X	q24	UniSTS
Cytogenetic Map	4	q25-q27	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	X	q26.2	UniSTS
Cytogenetic Map	8	q13.2	UniSTS
Cytogenetic Map	8	q13.1	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	5	q23.1	UniSTS
Cytogenetic Map	4	q13.3	UniSTS
Cytogenetic Map	3	p26.1	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	3	p22-p21.3	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	X	q21.3	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	20	p11	UniSTS
Cytogenetic Map	6	p12.3	UniSTS
Cytogenetic Map	5	p13.1-p12	UniSTS
Cytogenetic Map	1	p36.22	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	7	q21.13	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	3	p21.1-p14.3	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	7	q36.1	UniSTS
Cytogenetic Map	10	q24.31	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	13	q12.11	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	13	q14.13	UniSTS
Cytogenetic Map	11	p15	UniSTS
Cytogenetic Map	6	q14.3-q16.1	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	16	q22.3	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	8	p11	UniSTS
Cytogenetic Map	6	q25	UniSTS
Cytogenetic Map	8	p11.23	UniSTS
Cytogenetic Map	9	p24.3	UniSTS
Cytogenetic Map	7	q35	UniSTS
Cytogenetic Map	11	q22.3	UniSTS
Cytogenetic Map	16	p12	UniSTS
Cytogenetic Map	6	q14.3	UniSTS
Cytogenetic Map	7	q36	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	8	p12	UniSTS
Cytogenetic Map	13	q12.2	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	6	p21.2	UniSTS
Cytogenetic Map	18	q21.1	UniSTS
Cytogenetic Map	10	p11.21	UniSTS
Cytogenetic Map	10	p14	UniSTS
Cytogenetic Map	3	p26	UniSTS
Cytogenetic Map	9	q22.3	UniSTS
Cytogenetic Map	17	q21.1-q21.3	UniSTS
Cytogenetic Map	6	q11.1	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	3	q21.1	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	22	q13.1-q13.2	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	9	q32-q33.3	UniSTS
Cytogenetic Map	8	q21.2	UniSTS
Cytogenetic Map	18	q12.1	UniSTS
Cytogenetic Map	12	p13.2-p12.3	UniSTS
Cytogenetic Map	1	p36.3-p36.2	UniSTS
Cytogenetic Map	5	q11.2	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	3	q13.2	UniSTS
Cytogenetic Map	8	p22	UniSTS
Cytogenetic Map	1	q25.1	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	15	q26.2	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	5	p15.2	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	10	q24.2	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	1	p22.2	UniSTS
Cytogenetic Map	7	q32	UniSTS
Cytogenetic Map	5	p13	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	10	q24-q25	UniSTS
Cytogenetic Map	7	p11.1	UniSTS
Cytogenetic Map	14	q11.2-q21	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	12	q24.13	UniSTS
Cytogenetic Map	10	q21-q22	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	9	q22.2	UniSTS
Cytogenetic Map	10	q23.31	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	2	p24.1	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	7	p13-p11.1	UniSTS
Cytogenetic Map	7	q21.1-q22	UniSTS
Cytogenetic Map	1	p36.3	UniSTS
Cytogenetic Map	15	q26.1	UniSTS
Cytogenetic Map	2	q32.1	UniSTS
Cytogenetic Map	5	p14.3	UniSTS
Cytogenetic Map	X	p22.13	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
Cytogenetic Map	15	q	UniSTS
Cytogenetic Map	7	q	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	10	q23	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	10	q11.21	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	13	q22.1	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	9	p13.1	UniSTS
Cytogenetic Map	9	q34.13	UniSTS

D8S2279

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	21	q22.12	UniSTS
Cytogenetic Map	15	q13	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	15	q22.3	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	21	q21.3	UniSTS
Cytogenetic Map	3	p22-p21.3	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	2	q24.2	UniSTS
Cytogenetic Map	17	q24.2	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	20	q13.3	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	3	p14.1	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	7	p14.1	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	15	q13.2	UniSTS
Cytogenetic Map	12	q24.1	UniSTS
Cytogenetic Map	7	p15.2	UniSTS
Cytogenetic Map	5	q31.2	UniSTS
Cytogenetic Map	2	p25.2	UniSTS
Cytogenetic Map	3	p24.3	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	5	q14	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	1	p36.32	UniSTS
Cytogenetic Map	1	q42.12	UniSTS
Cytogenetic Map	7	q21.11	UniSTS
Cytogenetic Map	9	q34.2	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	8	q22.3	UniSTS
Cytogenetic Map	6	p21.1-p12	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	7	p21.3	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	22	q11.22	UniSTS
Cytogenetic Map	11	p13	UniSTS
Cytogenetic Map	1	q12	UniSTS
Cytogenetic Map	8	p23	UniSTS
Cytogenetic Map	11	q13.2-q13.3	UniSTS
Cytogenetic Map	13	q14.1-q14.3	UniSTS
Cytogenetic Map	3	q22-q24	UniSTS
Cytogenetic Map	3	q13.1-q13.2	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	5	q23.3-q31.1	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	14	q32.3	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	7	q32	UniSTS
Cytogenetic Map	14	q32.33	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	17	q11	UniSTS
Cytogenetic Map	17	p13.1-p12	UniSTS
Cytogenetic Map	18	q21.33	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	1	q21-q23	UniSTS
Cytogenetic Map	X	p11.23	UniSTS
Cytogenetic Map	4	q21.1	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	14	q23.3	UniSTS
Cytogenetic Map	17	p12-p11.2	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	1	q24	UniSTS
Cytogenetic Map	1	q43	UniSTS
Cytogenetic Map	9	q34.13	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	2	q32	UniSTS
Cytogenetic Map	X	p22.2	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	2	q33	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	3	q27	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
Cytogenetic Map	14	q22.3	UniSTS
Cytogenetic Map	10	q23-q24	UniSTS
Cytogenetic Map	2	q37.1	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	14	q31-q32	UniSTS
Cytogenetic Map	5	p15.33	UniSTS
Cytogenetic Map	1	q23.2	UniSTS
Cytogenetic Map	16	q24.3	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	2	q32.3	UniSTS
Cytogenetic Map	15	q21.1	UniSTS
Cytogenetic Map	4	q32.2	UniSTS
Cytogenetic Map	10	q23	UniSTS
Cytogenetic Map	5	q14.2	UniSTS
Cytogenetic Map	4	q32.1	UniSTS
Cytogenetic Map	1	q25.1	UniSTS
Cytogenetic Map	11	q14.1	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	3	p21.1	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	16	q11.2	UniSTS
Cytogenetic Map	6	q22	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	11	q23	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	19	q13.11	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	15	q15	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	22	q12.3	UniSTS
Cytogenetic Map	20	q11	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	3	p22.1	UniSTS
Cytogenetic Map	8	q22.1	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	18	p11.31	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	2	p22.1	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	1	p35.2	UniSTS
Cytogenetic Map	Y	p11.2	UniSTS
Cytogenetic Map	13	q13.1	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	18	q12	UniSTS
Cytogenetic Map	17	q21.33	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	3	q27.2	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	5	p15.2	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	1	q42	UniSTS
Cytogenetic Map	14	q32.11	UniSTS
Cytogenetic Map	17	q21.2-q21.3	UniSTS
Cytogenetic Map	5	q32-q34	UniSTS
Cytogenetic Map	15	q14	UniSTS
Cytogenetic Map	16	q13	UniSTS
Cytogenetic Map	3	q21.2	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	14	q24.2	UniSTS
Cytogenetic Map	12	q24.13	UniSTS
Cytogenetic Map	13	q14.11	UniSTS
Cytogenetic Map	3	q27.3	UniSTS
Cytogenetic Map	1	q32.3	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	6	q25.3	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	13	q14.3	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	10	p12	UniSTS
Cytogenetic Map	2	q33.3	UniSTS
Cytogenetic Map	14	q21.3	UniSTS
Cytogenetic Map	8	p22-p21	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	12	q21.33	UniSTS
Cytogenetic Map	20	q13.32	UniSTS
Cytogenetic Map	1	p34.1	UniSTS
Cytogenetic Map	10	q26	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	7	q21.13	UniSTS
Cytogenetic Map	7	q31.1	UniSTS
Cytogenetic Map	1	p33	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	9	q22.3	UniSTS
Cytogenetic Map	8	q13.1	UniSTS
Cytogenetic Map	3	q25	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	1	p31.3	UniSTS
Cytogenetic Map	14	q31.1	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	12	q13.2	UniSTS
Cytogenetic Map	22	q13.31-q13.33	UniSTS
Cytogenetic Map	20	q13.31	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	1	q41	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	17	q23.2	UniSTS
Cytogenetic Map	7	q32.2	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	14	q31-q32.1	UniSTS
Cytogenetic Map	1	q42.11	UniSTS
Cytogenetic Map	4	q35.1	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	X	p11.3	UniSTS
Cytogenetic Map	2	q11.2-q12.1	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	6	q16.2	UniSTS
Cytogenetic Map	18	q23	UniSTS
Cytogenetic Map	2	q14	UniSTS
Cytogenetic Map	20	p11.23-p11.21	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	8	p11.23	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	X	q26.3	UniSTS
Cytogenetic Map	8	q24.11	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	1	q44	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	9	q21.32	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	1	p36.1	UniSTS
Cytogenetic Map	20	q12	UniSTS
Cytogenetic Map	4	q21.23	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	22	q12.1	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	2	q21.3	UniSTS
Cytogenetic Map	7	q21.2	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	12	q24.11	UniSTS
Cytogenetic Map	18	q21	UniSTS
Cytogenetic Map	10	q11.1	UniSTS
Cytogenetic Map	22	q11.2	UniSTS
Cytogenetic Map	19	q12	UniSTS
Cytogenetic Map	7	q34-q35	UniSTS
Cytogenetic Map	15	q24.1	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	1	q23.1	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	6	p25.1-p23	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	18	q12.1-q21.1	UniSTS
Cytogenetic Map	12	p13.1	UniSTS
Cytogenetic Map	13	q12.1	UniSTS
Cytogenetic Map	12	q15	UniSTS
Cytogenetic Map	6	p21.32	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	10	p14	UniSTS
Cytogenetic Map	12	p13.1-p12.3	UniSTS
Cytogenetic Map	3	p25.2	UniSTS
Cytogenetic Map	6	p21.33	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	3	p21.2	UniSTS
Cytogenetic Map	10	q26.3	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	X	p21.2	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	9	q21.12	UniSTS
Cytogenetic Map	15	q23	UniSTS
Cytogenetic Map	7	p22.2	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	7	q33	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	4	q21.22	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	10	q24.31	UniSTS
Cytogenetic Map	12	p13.31	UniSTS
Cytogenetic Map	14	q32.12	UniSTS
Cytogenetic Map	10	q24.32	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	2	q24.3	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	3	q13.31	UniSTS
Cytogenetic Map	15	q22.2	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	6	q13	UniSTS
Cytogenetic Map	X	q24	UniSTS
Cytogenetic Map	6	q25	UniSTS
Cytogenetic Map	6	p21	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	12	p13-p12	UniSTS
Cytogenetic Map	9	p13.2	UniSTS
Cytogenetic Map	6	p22	UniSTS
Cytogenetic Map	2	q12.1	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	9	q22.2	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	1	p22.1	UniSTS
Cytogenetic Map	1	p36	UniSTS
Cytogenetic Map	9	q13-q21	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	X	p11.2	UniSTS
Cytogenetic Map	19	p	UniSTS
Cytogenetic Map	19	p13.1-p12	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	12	q24.33	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	8	q24	UniSTS
Cytogenetic Map	18	p11.31-p11.21	UniSTS
Cytogenetic Map	11	p15.3-p15.1	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	8	q22	UniSTS
Cytogenetic Map	4	p15.1	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	2	p16.3	UniSTS
Cytogenetic Map	16	p13.12	UniSTS
Cytogenetic Map	7	p21.2	UniSTS
Cytogenetic Map	12	q21.1	UniSTS
Cytogenetic Map	2	p14	UniSTS
Cytogenetic Map	6	q24.3	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	5	q23.1	UniSTS
Cytogenetic Map	10	q23.2	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	6	q22.1	UniSTS
Cytogenetic Map	1	q42.1	UniSTS
Cytogenetic Map	1	q25	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	15	q22.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	3	p21-p12	UniSTS
Cytogenetic Map	4	q35	UniSTS
Cytogenetic Map	1	p34-p33	UniSTS
Cytogenetic Map	21	q22.11	UniSTS
Cytogenetic Map	3	p22-p21.33	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	3	q22.1	UniSTS
Cytogenetic Map	8	q21.11	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	7	p14	UniSTS
Cytogenetic Map	17	q21.1	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	1	q42.3	UniSTS
Cytogenetic Map	9	q22	UniSTS
Cytogenetic Map	2	q12.3	UniSTS
Cytogenetic Map	20	q11.2-q13.2	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	17	q24	UniSTS
Cytogenetic Map	3	q25.31	UniSTS
Cytogenetic Map	6	p24.3	UniSTS
Cytogenetic Map	2	q31.3	UniSTS
Cytogenetic Map	1	q31	UniSTS
Cytogenetic Map	7	q32-q33	UniSTS
Cytogenetic Map	7	q21.1	UniSTS
Cytogenetic Map	14	q23-q24.2	UniSTS
Cytogenetic Map	19	q13.3-q13.4	UniSTS
Cytogenetic Map	2	p24-p21	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	15	q26.3	UniSTS
Cytogenetic Map	7	p22	UniSTS
Cytogenetic Map	12	p11	UniSTS
Cytogenetic Map	1	p35.3	UniSTS
Cytogenetic Map	1	p12	UniSTS
Cytogenetic Map	13	q32.3	UniSTS
Cytogenetic Map	5	q23.3	UniSTS
Cytogenetic Map	20	q13	UniSTS
Cytogenetic Map	17	q25.2	UniSTS
Cytogenetic Map	7	q36.1	UniSTS
Cytogenetic Map	10	p12.33	UniSTS
Cytogenetic Map	17	q21.32	UniSTS
Cytogenetic Map	X	p11.22	UniSTS
Cytogenetic Map	12	p13.3	UniSTS
Cytogenetic Map	X	q25-q26	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	5	p13	UniSTS
Cytogenetic Map	15	q25	UniSTS
Cytogenetic Map	5	q12.1	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	1	p36.22	UniSTS
Cytogenetic Map	3	q26.31	UniSTS
Cytogenetic Map	17	q22-q23	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	X	q13.2	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	16	q12.2	UniSTS
Cytogenetic Map	3	q26.32	UniSTS
Cytogenetic Map	6	q22.31	UniSTS
Cytogenetic Map	3	q26.2-q27	UniSTS
Cytogenetic Map	1	q25.1-q25.2	UniSTS
Cytogenetic Map	14	q24	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	10	q11.22	UniSTS
Cytogenetic Map	22	q13.31	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	5	q21.3	UniSTS
Cytogenetic Map	5	p13.3	UniSTS
Cytogenetic Map	10	q22.1	UniSTS
Cytogenetic Map	14	q12-q13	UniSTS
Cytogenetic Map	X	p22	UniSTS
Cytogenetic Map	X	q23	UniSTS
Cytogenetic Map	20	p12.3-p11.21	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	17	q11.2-q12	UniSTS
Cytogenetic Map	4	q32-q34	UniSTS
Cytogenetic Map	X	q25-q26.1	UniSTS
Cytogenetic Map	2	p25-p24	UniSTS
Cytogenetic Map	2	p25	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	X	p22.2-p22.1	UniSTS
Cytogenetic Map	X	q22.1	UniSTS
Cytogenetic Map	4	q25	UniSTS
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	22	q13	UniSTS
Cytogenetic Map	20	q11.22-q12	UniSTS
Cytogenetic Map	4	q34.2	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	22	q13.1-q13.2	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	12	q13-q14	UniSTS
Cytogenetic Map	6	q14.1	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	9	q31.2	UniSTS
Cytogenetic Map	11	q13.1-q13.2	UniSTS
Cytogenetic Map	12	q13	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	21	q21.2	UniSTS
Cytogenetic Map	10	q24.3	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	8	q21.1	UniSTS
Cytogenetic Map	5	p13.2	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	1	q32.2	UniSTS
Cytogenetic Map	4	q21.3	UniSTS
Cytogenetic Map	7	q21-q22	UniSTS
Cytogenetic Map	3	q26.2	UniSTS
Cytogenetic Map	2	q36.3	UniSTS
Cytogenetic Map	8	p22	UniSTS
Cytogenetic Map	11	q22.1	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	10	q23.31	UniSTS
Cytogenetic Map	4	p15.32	UniSTS
Cytogenetic Map	18	q12.2	UniSTS
Cytogenetic Map	15	q15.2	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	12	q14.1	UniSTS
Cytogenetic Map	6	p22.3-p22.1	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	6	q15	UniSTS
Cytogenetic Map	6	q23.3	UniSTS
Cytogenetic Map	13	q14	UniSTS
Cytogenetic Map	5	q35.2	UniSTS
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	1	p35	UniSTS
Cytogenetic Map	3	q12.3	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	8	q23.1	UniSTS
Cytogenetic Map	6	q27	UniSTS
Cytogenetic Map	2	q14.3	UniSTS
Cytogenetic Map	X	p11	UniSTS
Cytogenetic Map	11	p15.3	UniSTS
Cytogenetic Map	20	p12	UniSTS
Cytogenetic Map	15	q13.1	UniSTS
Cytogenetic Map	X	p22.3	UniSTS
Cytogenetic Map	11	q13.5	UniSTS
Cytogenetic Map	19	p13.3-p13.2	UniSTS
Cytogenetic Map	1	p36.11-p34.2	UniSTS
Cytogenetic Map	4	q22.1-q23	UniSTS
Cytogenetic Map	7	q22.3	UniSTS
Cytogenetic Map	9	p22	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	2	p22.3	UniSTS
Cytogenetic Map	X	q26.1	UniSTS
Cytogenetic Map	4	q21.21	UniSTS
Cytogenetic Map	22	q13.3	UniSTS
Cytogenetic Map	2	q32.1	UniSTS
Cytogenetic Map	Y	p11.32	UniSTS
Cytogenetic Map	11	p14	UniSTS
Cytogenetic Map	1	p32.1	UniSTS
Cytogenetic Map	2	p25.3	UniSTS
Cytogenetic Map	4	q34.3	UniSTS
Cytogenetic Map	9	p12	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	13	q34	UniSTS
Cytogenetic Map	3	p21	UniSTS
Cytogenetic Map	11	q23.2	UniSTS
Cytogenetic Map	20	p11.23	UniSTS
Cytogenetic Map	3	p13	UniSTS
Cytogenetic Map	4	p13	UniSTS
Cytogenetic Map	16	q23.1	UniSTS
Cytogenetic Map	10	p11.23	UniSTS
Cytogenetic Map	8	p21.1	UniSTS
Cytogenetic Map	15	q22-q24	UniSTS
Cytogenetic Map	8	q23	UniSTS
Cytogenetic Map	16	q12.1	UniSTS
Cytogenetic Map	14	q13.2	UniSTS
Cytogenetic Map	18	q12.1	UniSTS
Cytogenetic Map	5	q31.3	UniSTS
Cytogenetic Map	11	q14	UniSTS
Cytogenetic Map	13	q33.1	UniSTS
Cytogenetic Map	14	q21.2	UniSTS
Cytogenetic Map	4	q31.3	UniSTS
Cytogenetic Map	15	q21-q22	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	13	q12.11	UniSTS
Cytogenetic Map	6	p21.2	UniSTS
Cytogenetic Map	15	q21.3	UniSTS
Cytogenetic Map	3	q21.1	UniSTS
Cytogenetic Map	6	p21.31	UniSTS
Cytogenetic Map	10	p15.1	UniSTS
Cytogenetic Map	1	q24.2	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	21	q22.13	UniSTS
Cytogenetic Map	15	q22.1-q22.31	UniSTS
Cytogenetic Map	15	q22	UniSTS
Cytogenetic Map	X	q13	UniSTS
Cytogenetic Map	1	q31-q41	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	14	q32.1	UniSTS
Cytogenetic Map	16	q12-q13	UniSTS
Cytogenetic Map	X	q12-q13	UniSTS
Cytogenetic Map	14	q23	UniSTS
Cytogenetic Map	12	q11-q12	UniSTS
Cytogenetic Map	1	q42.1-q43	UniSTS
Cytogenetic Map	3	q13.33	UniSTS
Cytogenetic Map	7	q31	UniSTS
Cytogenetic Map	12	q24	UniSTS
Cytogenetic Map	X	p22.11	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	8	q24.21	UniSTS
Cytogenetic Map	12	q13.1	UniSTS
Cytogenetic Map	12	q22-q23.1	UniSTS
Cytogenetic Map	11	q12.2	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	5	q31.2-q34	UniSTS
Cytogenetic Map	11	p15.1	UniSTS
Cytogenetic Map	6	q24.2	UniSTS
Cytogenetic Map	22	q	UniSTS
Cytogenetic Map	12	q13.11-q14.3	UniSTS
Cytogenetic Map	7	p11	UniSTS
Cytogenetic Map	X	p22.12-p22.11	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	20	q11.22-q11.23	UniSTS
Cytogenetic Map	8	q24.22	UniSTS
Cytogenetic Map	8	p22-p21.3	UniSTS
Cytogenetic Map	10	q24	UniSTS
Cytogenetic Map	1	q21.2-q21.3	UniSTS
Cytogenetic Map	1	p36.12	UniSTS
Cytogenetic Map	9	p24.1	UniSTS
Cytogenetic Map	6	q25.2-q27	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	5	p13.1	UniSTS
Cytogenetic Map	8	q11.2	UniSTS
Cytogenetic Map	3	q28-q29	UniSTS
Cytogenetic Map	7	p14-p13	UniSTS
Cytogenetic Map	12	q24.2	UniSTS
Cytogenetic Map	6	p22.2	UniSTS
Cytogenetic Map	7	q22-qter	UniSTS
Cytogenetic Map	12	q24.2-q24.31	UniSTS
Cytogenetic Map	X	q13.1	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	1	p21	UniSTS
Cytogenetic Map	1	q32.2-q41	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	12	q23-q24.1	UniSTS
Cytogenetic Map	5	p15.1-p14.3	UniSTS
Cytogenetic Map	16	p13.11	UniSTS
Cytogenetic Map	6	q22-q23	UniSTS
Cytogenetic Map	9	p21	UniSTS
Cytogenetic Map	6	p12.3	UniSTS
Cytogenetic Map	3	p12.1	UniSTS
Cytogenetic Map	9	q21.11	UniSTS
Cytogenetic Map	17	q24.1	UniSTS
Cytogenetic Map	10	q11.21	UniSTS
Cytogenetic Map	14	q21	UniSTS
Cytogenetic Map	11	p15	UniSTS
Cytogenetic Map	16	q22	UniSTS
Cytogenetic Map	15	q11-q13	UniSTS
Cytogenetic Map	13	q12-q14	UniSTS
Cytogenetic Map	18	q21.1	UniSTS
Cytogenetic Map	2	q24	UniSTS
Cytogenetic Map	12	p13	UniSTS
Cytogenetic Map	3	q28	UniSTS
Cytogenetic Map	7	q32.1	UniSTS
Cytogenetic Map	X	q22.2	UniSTS
Cytogenetic Map	7	p12.3	UniSTS
Cytogenetic Map	7	p15.1	UniSTS
Cytogenetic Map	2	q37.2	UniSTS
Cytogenetic Map	18	q22.3	UniSTS
Cytogenetic Map	14	q32.13	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	16	p13.1	UniSTS
Cytogenetic Map	7	q31.3	UniSTS
Cytogenetic Map	20	q13.2-q13.3	UniSTS
Cytogenetic Map	1	p21.2	UniSTS
Cytogenetic Map	9	q21.33	UniSTS
Cytogenetic Map	14	q32.2	UniSTS
Cytogenetic Map	13	q13.3	UniSTS
Cytogenetic Map	10	p12.31	UniSTS
Cytogenetic Map	22	q11.1	UniSTS
Cytogenetic Map	5	q33.2	UniSTS
Cytogenetic Map	13	q32.2	UniSTS
Cytogenetic Map	14	q23.1	UniSTS
Cytogenetic Map	8	q21.2	UniSTS
Cytogenetic Map	2	q24.1	UniSTS
Cytogenetic Map	10	q26.13	UniSTS
Cytogenetic Map	2	q23.3	UniSTS
Cytogenetic Map	19	p13.1	UniSTS
Cytogenetic Map	15	q14-q15	UniSTS
Cytogenetic Map	1	q42.13	UniSTS
Cytogenetic Map	14	q31	UniSTS
Cytogenetic Map	7	p21.1	UniSTS
Cytogenetic Map	8	p12-p11	UniSTS
Cytogenetic Map	18	p11.2	UniSTS
Cytogenetic Map	7	p11.1	UniSTS
Cytogenetic Map	1	q31-q32	UniSTS
Cytogenetic Map	2	q12	UniSTS
Cytogenetic Map	3	p21.32	UniSTS
Cytogenetic Map	2	p24.2	UniSTS
Cytogenetic Map	2	q33-q34	UniSTS
Cytogenetic Map	6	q24.1	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	15	q13.3	UniSTS
Cytogenetic Map	10	q26.11	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	10	q23.33	UniSTS
Cytogenetic Map	12	p12.1	UniSTS
Cytogenetic Map	7	p13-p12	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	17	q11-q21	UniSTS
Cytogenetic Map	12	q23	UniSTS
Cytogenetic Map	6	p24-p22.3	UniSTS
Cytogenetic Map	14	q23.2	UniSTS
Cytogenetic Map	7	q31.1-q31.2	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	3	p26.1-p25.1	UniSTS
Cytogenetic Map	5	q35	UniSTS
Cytogenetic Map	3	q13.2	UniSTS
Cytogenetic Map	4	p15.2	UniSTS
Cytogenetic Map	6	q16.3	UniSTS
Cytogenetic Map	17	q24-q25	UniSTS
Cytogenetic Map	X	q12	UniSTS
Cytogenetic Map	X	q27.1	UniSTS
Cytogenetic Map	8	q12.3	UniSTS
Cytogenetic Map	5	q21.2	UniSTS
Cytogenetic Map	5	q15	UniSTS
Cytogenetic Map	5	q35.1	UniSTS
Cytogenetic Map	4	q13.3	UniSTS
Cytogenetic Map	4	q35.2	UniSTS
Cytogenetic Map	3	p26.1	UniSTS
Cytogenetic Map	3	p11.1	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	2	q21.2	UniSTS
Cytogenetic Map	19	p13.13	UniSTS
Cytogenetic Map	18	q12.3	UniSTS
Cytogenetic Map	18	p11.3	UniSTS
Cytogenetic Map	17	q11.1	UniSTS
Cytogenetic Map	15	q25.1	UniSTS
Cytogenetic Map	13	q12.3	UniSTS
Cytogenetic Map	12	q23.2	UniSTS
Cytogenetic Map	12	q12-q13	UniSTS
Cytogenetic Map	12	q14	UniSTS
Cytogenetic Map	5	q33.1	UniSTS
Cytogenetic Map	2	q32-q34	UniSTS
Cytogenetic Map	16	q22.3	UniSTS
Cytogenetic Map	2	p15-p13	UniSTS
Cytogenetic Map	X	p11.4	UniSTS
Cytogenetic Map	19	q13.33-q13.41	UniSTS
Cytogenetic Map	20	p11	UniSTS
Cytogenetic Map	6	q23-q24	UniSTS
Cytogenetic Map	2	p12	UniSTS
Cytogenetic Map	2	p13	UniSTS
Cytogenetic Map	13	q11-q12	UniSTS
Cytogenetic Map	6	p12.3-p11.2	UniSTS
Cytogenetic Map	6	q16.1-q16.3	UniSTS
Cytogenetic Map	22	q11	UniSTS
Cytogenetic Map	7	q31.2	UniSTS
Cytogenetic Map	10	q21.3	UniSTS
Cytogenetic Map	3	q25.2	UniSTS
Cytogenetic Map	3	p21.1-p14.3	UniSTS
Cytogenetic Map	6	p12.1	UniSTS
Cytogenetic Map	3	q23-q24	UniSTS
Cytogenetic Map	3	q12	UniSTS
Cytogenetic Map	7	q11.1	UniSTS
Cytogenetic Map	3	q22.3	UniSTS
Cytogenetic Map	7	q21.3	UniSTS
Cytogenetic Map	4	q31.1	UniSTS
Cytogenetic Map	22	q12-q13	UniSTS
Cytogenetic Map	4	q23	UniSTS
Cytogenetic Map	X	p22.12	UniSTS
Cytogenetic Map	6	q16.1	UniSTS
Cytogenetic Map	13	q14.13	UniSTS
Cytogenetic Map	18	q21.3	UniSTS
Cytogenetic Map	9	q33.2	UniSTS
Cytogenetic Map	11	q21	UniSTS
Cytogenetic Map	8	q12	UniSTS
Cytogenetic Map	4	q28-q32	UniSTS
Cytogenetic Map	17	q24.3	UniSTS
Cytogenetic Map	6	p23	UniSTS
Cytogenetic Map	8	p11	UniSTS
Cytogenetic Map	5	q34	UniSTS
Cytogenetic Map	1	q24.3	UniSTS
Cytogenetic Map	9	q33.1	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	2	p16.2	UniSTS
Cytogenetic Map	9	q22.31	UniSTS
Cytogenetic Map	9	p24.3	UniSTS
Cytogenetic Map	7	q35	UniSTS
Cytogenetic Map	1	p36.2	UniSTS
Cytogenetic Map	11	q22.3	UniSTS
Cytogenetic Map	16	p12	UniSTS
Cytogenetic Map	1	q22-q23	UniSTS
Cytogenetic Map	13	q22.1	UniSTS
Cytogenetic Map	2	q12.2	UniSTS
Cytogenetic Map	8	p12	UniSTS
Cytogenetic Map	4	q21	UniSTS
Cytogenetic Map	13	q12.2	UniSTS
Cytogenetic Map	9	q31-q33	UniSTS
Cytogenetic Map	6	p24.1	UniSTS
Cytogenetic Map	1	q23	UniSTS
Cytogenetic Map	11	q12-q13	UniSTS
Cytogenetic Map	11	q13.3	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	11	q12.1	UniSTS
Cytogenetic Map	3	p26	UniSTS
Cytogenetic Map	5	q13	UniSTS
Cytogenetic Map	8	p21	UniSTS
Cytogenetic Map	19	q13.1-q13.2	UniSTS
Cytogenetic Map	1	p33-p32	UniSTS
Cytogenetic Map	7	q36.2	UniSTS
Cytogenetic Map	4	q32.3	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	10	q26.1	UniSTS
Cytogenetic Map	9	q32-q33.3	UniSTS
Cytogenetic Map	9	q22.1-q22.2	UniSTS
Cytogenetic Map	3	q26.1-q26.2	UniSTS
Cytogenetic Map	5	q31-q34	UniSTS
Cytogenetic Map	9	q33-q34	UniSTS
Cytogenetic Map	5	q11.2-q13.2	UniSTS
Cytogenetic Map	13	q32	UniSTS
Cytogenetic Map	9	q22.32	UniSTS
Cytogenetic Map	1	p36.3	UniSTS
Cytogenetic Map	1	p36.3-p36.2	UniSTS
Cytogenetic Map	4	q28.1	UniSTS
Cytogenetic Map	5	q22	UniSTS
Cytogenetic Map	12	p11.21	UniSTS
Cytogenetic Map	X	q13.3	UniSTS
Cytogenetic Map	9	q31.3	UniSTS
Cytogenetic Map	3	p26.3	UniSTS
Cytogenetic Map	2	q11.1	UniSTS
Cytogenetic Map	21	q11.2	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	15	q26.2	UniSTS
Cytogenetic Map	12	q24.23	UniSTS
Cytogenetic Map	10	q25.3	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	20	p12.1	UniSTS
Cytogenetic Map	2	q31.1-q31.2	UniSTS
Cytogenetic Map	X	p22.31	UniSTS
Cytogenetic Map	X	p21.3	UniSTS
Cytogenetic Map	5	q33.3	UniSTS
Cytogenetic Map	4	q28.2	UniSTS
Cytogenetic Map	3	p14.2	UniSTS
Cytogenetic Map	3	q24	UniSTS
Cytogenetic Map	2	q13	UniSTS
Cytogenetic Map	20	q13.2	UniSTS
Cytogenetic Map	14	q11.2-q12	UniSTS
Cytogenetic Map	3	p24	UniSTS
Cytogenetic Map	12	q23.3	UniSTS
Cytogenetic Map	11	q24.3	UniSTS
Cytogenetic Map	11	q14.3	UniSTS
Cytogenetic Map	10	q25.2	UniSTS
Cytogenetic Map	3	q25.1	UniSTS
Cytogenetic Map	8	q13	UniSTS
Cytogenetic Map	1	p22.2	UniSTS
Cytogenetic Map	3	p22.3	UniSTS
Cytogenetic Map	18	q11.1	UniSTS
Cytogenetic Map	8	q23.3	UniSTS
Cytogenetic Map	15	q24	UniSTS
Cytogenetic Map	11	cen-q12	UniSTS
Cytogenetic Map	11	q25	UniSTS
Cytogenetic Map	3	p22.2	UniSTS
Cytogenetic Map	X	p21.1	UniSTS
Cytogenetic Map	7	q36	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	12	q21	UniSTS
Cytogenetic Map	7	p15	UniSTS
Cytogenetic Map	7	q22-q31	UniSTS
Cytogenetic Map	11	q22	UniSTS
Cytogenetic Map	5	p15.3	UniSTS
Cytogenetic Map	20	q13.3-qter	UniSTS
Cytogenetic Map	1	p35-p34	UniSTS
Cytogenetic Map	4	p13-p12	UniSTS
Cytogenetic Map	10	q21-q22	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	7	p13-p11.1	UniSTS
Cytogenetic Map	9	q31-q34	UniSTS
Cytogenetic Map	7	q21.1-q22	UniSTS
Cytogenetic Map	15	q26.1	UniSTS
Cytogenetic Map	3	q13.13-q13.2	UniSTS
Cytogenetic Map	X	p22.13	UniSTS
Cytogenetic Map	13	q12.12	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	1	p	UniSTS
Cytogenetic Map	16	p	UniSTS
Cytogenetic Map	15	q	UniSTS
Cytogenetic Map	7	q	UniSTS
Cytogenetic Map	2	q	UniSTS
Cytogenetic Map	5	q13.1	UniSTS
Cytogenetic Map	11	p14.1	UniSTS
Cytogenetic Map	4	q32	UniSTS
Cytogenetic Map	2	p22	UniSTS
Cytogenetic Map	5	q14.3	UniSTS
Cytogenetic Map	10	p12.1	UniSTS
Cytogenetic Map	5	q23.2	UniSTS
Cytogenetic Map	2	p24.1	UniSTS
Cytogenetic Map	8	q24.13	UniSTS
Cytogenetic Map	12	p13.32	UniSTS
Cytogenetic Map	9	p21.1	UniSTS
Cytogenetic Map	9	q34.2-q34.3	UniSTS

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2437	2788	2250	4972	1722	2347	6	620	1841	461	2268	7187	6359	52	3734	1	851	1743	1617	174	1


RefSeq Transcripts	NM_001384285	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384286	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384287	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384288	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384289	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384291	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384292	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384293	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384294	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384295	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384296	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384297	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384298	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384300	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384301	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384302	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384303	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384304	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384305	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384306	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384307	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384308	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384309	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384310	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384311	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384312	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001384313	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_152505	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529458	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529459	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529460	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529461	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529462	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529463	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529464	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529465	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529466	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529467	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529468	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529469	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529470	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529471	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028274	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028277	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440684	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440685	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440686	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440687	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440688	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440689	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440690	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440691	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440692	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440693	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440694	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440695	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440696	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440697	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440698	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324335	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324336	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324337	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324338	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324339	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324340	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324341	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324342	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324343	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324344	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324345	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324346	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324347	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324348	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324349	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324350	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324351	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324352	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324353	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324354	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324355	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324356	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324357	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324358	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324359	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324360	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324361	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AF121781	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK123810	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL163279	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC026122	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC031059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC043006	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX647793	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX648744	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471079	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068257	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000288350 ⟹ ENSP00000288350

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,405,728 - 39,445,778 (-)	Ensembl

Ensembl Acc Id:

ENST00000358268 ⟹ ENSP00000351008

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,405,860 - 39,445,733 (-)	Ensembl

Ensembl Acc Id:

ENST00000380671 ⟹ ENSP00000370046

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,405,844 - 39,428,522 (-)	Ensembl

Ensembl Acc Id:

ENST00000411566 ⟹ ENSP00000412691

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,428,215 - 39,445,733 (-)	Ensembl

Ensembl Acc Id:

ENST00000415863 ⟹ ENSP00000395593

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,428,285 - 39,445,769 (-)	Ensembl

Ensembl Acc Id:

ENST00000418018 ⟹ ENSP00000404521

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,423,245 - 39,445,760 (-)	Ensembl

Ensembl Acc Id:

ENST00000426783 ⟹ ENSP00000414784

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,428,305 - 39,445,769 (-)	Ensembl

Ensembl Acc Id:

ENST00000434281 ⟹ ENSP00000400086

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,428,208 - 39,445,803 (-)	Ensembl

Ensembl Acc Id:

ENST00000438404 ⟹ ENSP00000405130

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,428,210 - 39,445,719 (-)	Ensembl

Ensembl Acc Id:

ENST00000448288 ⟹ ENSP00000405598

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,428,172 - 39,445,778 (-)	Ensembl

Ensembl Acc Id:

ENST00000451131 ⟹ ENSP00000401084

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,428,462 - 39,445,752 (-)	Ensembl

Ensembl Acc Id:

ENST00000456017 ⟹ ENSP00000407065

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,428,402 - 39,445,780 (-)	Ensembl

Ensembl Acc Id:

ENST00000459939

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,422,988 - 39,445,761 (-)	Ensembl

Ensembl Acc Id:

ENST00000466954

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,423,420 - 39,445,733 (-)	Ensembl

Ensembl Acc Id:

ENST00000468009

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,428,222 - 39,438,936 (-)	Ensembl

Ensembl Acc Id:

ENST00000480612

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,443,459 - 39,445,753 (-)	Ensembl

Ensembl Acc Id:

ENST00000484878

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,411,718 - 39,445,752 (-)	Ensembl

Ensembl Acc Id:

ENST00000485895 ⟹ ENSP00000475187

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,421,560 - 39,445,777 (-)	Ensembl

Ensembl Acc Id:

ENST00000490184

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,423,240 - 39,445,775 (-)	Ensembl

Ensembl Acc Id:

ENST00000491625

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,422,412 - 39,445,805 (-)	Ensembl

Ensembl Acc Id:

ENST00000495240

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	21	39,405,978 - 39,411,147 (-)	Ensembl

RefSeq Acc Id:

NM_001384285 ⟹ NP_001371214

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATA
AATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGA
TGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCA
AGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTC
TGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATCAGTTGA
AAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAAT
TAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATG
GCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCA
GGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGA
GGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGAT
CGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAG
TATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGA
ATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAA
AAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAG
AAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGG
GGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATA
AAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCA
AAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTA
TTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAATGCTGCTTATGTGCCTTGCATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGTATGTATGTGTGTGTTTTAGTACTTAATTGACT
TTCGATAATTAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

NM_001384286 ⟹ NP_001371215

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGTTTTTTAAA
ATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTT
TAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACA
AAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGA
TTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAA
AGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGA
AGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACT
TCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGG
AAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAA
TTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGC
TCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAG
AGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAG
GCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAA
ACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTC
ATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGA
CAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAG
AGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGAT
CAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGAC
TCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAATGCTGCTTATGTGCCTTG
CATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGTATGTATGTGTGTGTTTTAGTACTTAATTGACTTTCGATAATTAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

NM_001384287 ⟹ NP_001371216

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTAT
CTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTG
AGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTC
ACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATA
GAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTC
TTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGC
CATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATT
TAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAA
AACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCA
GCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATA
GTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCA
GATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAA
GAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGC
AAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAA
GGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTA
CAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATA
AGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCC
AGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCAT
TCTGGTTTGATATAATGCTGCTTATGTGCCTTGCATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGTATGTATGTGTGTGTTTTAGTACTTAATTGACTTTCGATAATTAAATTTTTGTTTGATTGC
TAA

hide sequence

RefSeq Acc Id:

NM_001384288 ⟹ NP_001371217

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGTAACGGCCC
CGCTGCTGCCGTCGTCCCCCTCAGCCGGTTACCCTGTTACAGCCCCAGCTCTGGGCCCTTCCGGACCCTCCTGCTACGCTCTTTCTGGGCTTCCAGTATCGCCGGTCACTCAGTCCTCGCCCCTGCCT
GCCTCGCTGGCGCCCCGCCGTTTCCTCCTCGCGGCACAGTTTGCCAAGGAACAGCTACCCCGGCTCGGCAGTGACCGGGCGCCCCGGCGACACACGTACTCTCAGGCCCGCTGGGCAGGGGGACGGCC
TGGGCCGAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAA
ATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGT
AAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAA
AACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCA
GTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTA
AAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCAT
AAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTC
ACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGT
TACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAA
ATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCT
TCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAG
ACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATA
AATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACA
AAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAG
AAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTG
CATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCC
CTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTG
CAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCT
ACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAATGCTGCTTATGTGCCTTGCATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGTATGTATG
TGTGTGTTTTAGTACTTAATTGACTTTCGATAATTAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

NM_001384289 ⟹ NP_001371218

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGTTTTTTAAA
ATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTT
TAATAAAGAACACCAGTGAGGAGATTGTGGACTGCCTAATATATTTCATCAGAAGAGAAGGCTGGAGAATTAAGCAGATGCAGCAAAAAGCAGAAACTGACTTCAAAAAAAACCCTCTCAGTAGAGAA
AGTGATATTAGATTCCTATTGCAAAGGATCTAATGCCAGTTAAATTCTCTTTTGCTTTCTTGATAAAACAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATC
TGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAA
GCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGAT
TGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATCAGTTGAAAAAAA
GCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTG
ATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAA
CATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACT
GCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGA
ACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAG
CTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAG
ACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAAC
TACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAA
AACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGG
TGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAG
CCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTG
AAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAA
GGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAA
TATAATCAATATCCTAATGCATTCTGGTTTGATATAATGCTGCTTATGTGCCTTGCATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGTATGTATGTGTGTGTTTTAGTACTTAATTGACTTTCGAT
AATTAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

NM_001384291 ⟹ NP_001371220

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGTAACGGCCC
CGCTGCTGCCGTCGTCCCCCTCAGCCGGTTACCCTGTTACAGCCCCAGCTCTGGGCCCTTCCGGACCCTCCTGCTACGCTCTTTCTGGGCTTCCAGTATCGCCGGTCACTCAGTCCTCGCCCCTGCCT
GCCTCGCTGGCGCCCCGCCGTTTCCTCCTCGCGGCACAGTTTGCCAAGGAACAGCTACCCCGGCTCGGCAGTGACCGGGCGCCCCGGCGACACACGTACTCTCAGGCCCGCTGGGCAGGGGGACGGCC
TGGGCCGAGGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCAT
CAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTAT
GTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATG
CTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAG
CAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAAT
CCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAA
ACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTT
AGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAG
GGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGA
CTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTT
AAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTT
GACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAG
ATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCA
AAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTA
CACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAG
GCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTC
ATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCAC
CAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATA
ATGCTGCTTATGTGCCTTGCATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGTATGTATGTGTGTGTTTTAGTACTTAATTGACTTTCGATAATTAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

NM_001384292 ⟹ NP_001371221

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGC
TTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCT
TCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGA
ATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGC
CAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAA
AAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAAC
ACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAA
GCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGA
AATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAA
GACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTA
AGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAA
CCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATG
AGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGT
GTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTC
ACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAATGCTGCTTATGTGCCTTGCATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGTATG
TATGTGTGTGTTTTAGTACTTAATTGACTTTCGATAATTAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

NM_001384293 ⟹ NP_001371222

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCA
AAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTC
ATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTC
AGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCT
ATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAG
GCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTC
TATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATT
ATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGC
TACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATC
CAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGA
AACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGA
AGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAA
GAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGA
CATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAAT
GGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATG
TCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTA
ACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAATGCTGCTTATGTGCCTTGCATCTTATT
TTTGAAATGTGTGAGAGAGGGAGTGTATGTATGTGTGTGTTTTAGTACTTAATTGACTTTCGATAATTAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

NM_001384294 ⟹ NP_001371223

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGCCAGAA
GGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAG
GACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAAT
CTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGAC
TAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCT
TGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAA
CTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAAT
TTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAA
TTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAA
AAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAA
AAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGC
TTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGT
AAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTC
AGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAA
AAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAATGCTGCTTATGTGCCTTGCATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGTATGTATGTGTGTGTTTT
AGTACTTAATTGACTTTCGATAATTAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

NM_001384295 ⟹ NP_001371224

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCA
AAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATC
TGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAG
GCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATG
AGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGAC
AGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGA
CAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAA
AACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTC
CAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAAC
TGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTG
GAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTA
GTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGA
AAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGT
ATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCT
GGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATC
GTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAATGCTGCTTATGTGCCTTGCATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGT
ATGTATGTGTGTGTTTTAGTACTTAATTGACTTTCGATAATTAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

NM_001384296 ⟹ NP_001371225

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGTTTTTTAAA
ATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTT
TAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCA
CACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATA
TGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACAT
CAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCA
GAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACT
GCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTT
GAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACA
CCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTAC
CAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAAC
ATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGT
GGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCA
ATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAG
GATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGA
GTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATAT
AATCAATATCCTAATGCATTCTGGTTTGATATAATGCTGCTTATGTGCCTTGCATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGTATGTATGTGTGTGTTTTAGTACTTAATTGACTTTCGATAAT
TAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

NM_001384297 ⟹ NP_001371226

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGTCTGTCAGCA
CTGCCTTCAAAATGCACCCAGAATAGATTCACAATTCTACCATTTCTCTCAACCGCCACTGTCACCACCTTGGTCCAGGCCCCCATCATCTGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAA
ATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCT
GTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATC
TGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGC
GATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGC
TATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATG
CATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAA
TTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGT
AAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTG
AAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAA
GTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTG
GTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGC
TAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGT
TCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAA
ATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCT
TACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTC
GTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCT
TGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACA
TAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTT
CTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTA
AAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384298 ⟹ NP_001371227

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGAGAATT
GAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTT
CTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCT
GTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTT
TCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAAT
ACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTA
TAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTT
AGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAAT
GGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAAC
TGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTT
CACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTC
AACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTA
TTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGAT
TACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTC
TGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAA
TTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTG
TCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAA
ATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATG
TCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAAT
AAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384299 ⟹ NP_001371228

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCA
AAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAATGAAAAGCGGAATCTAATTTGCATTTCATTATGAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACC
AAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAG
AATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTTTACTTTTCTTTTATTAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAAC
AAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATA
GCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAG
AAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGA
TGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGC
TTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGA
ACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATC
TATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTG
TAACAAAGCATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTG
TTGCAGTGCACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTG
AAACCTCTCTTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCA
CACAGACATTTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGT
TGTCAAAAGCCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAAT
TAATTTAGGATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAAT
TCCCTATTTTCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATT
CATCTTAGCGTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGC
ACTTACCAAGTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTC
CCCTTGTAGCTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAG
ATCTAACAGTTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384300 ⟹ NP_001371229

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCA
AAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTC
ATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTC
AGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAG
CATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGAC
TTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATC
AGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAA
ATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAA
ATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATAT
CTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAG
GGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGT
CTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCAT
TCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTC
CCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGG
GTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATAT
CATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGA
TCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAA
TAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAA
GTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACT
GTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTAT
AATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384301 ⟹ NP_001371230

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGTAACGGCCCCGCTGCTGCCGTCGTCCCCCTCAGCCGGTTACCCTGTTACAGCCCCAGCTCTGGGCCCTTCCGG
ACCCTCCTGCTACGCTCTTTCTGGGCTTCCAGTATCGCCGGTCACTCAGTCCTCGCCCCTGCCTGCCTCGCTGGCGCCCCGCCGTTTCCTCCTCGCGGCACAGTTTGCCAAGGAACAGCTACCCCGGC
TCGGCAGTGACCGGGCGCCCCGGCGACACACGTACTCTCAGGCCCGCTGGGCAGGGGGACGGCCTGGGCCGAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGA
TCATTTTGAATAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTAT
CATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGC
TATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTA
ATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTA
AAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCA
AATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAG
AAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTA
CTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGA
AAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGT
GAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAA
GCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGT
GCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTC
CCTCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTG
GATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGT
CTGTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAAT
CTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATT
ATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCC
ATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTA
GGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCC
TTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384302 ⟹ NP_001371231

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATA
AATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGA
AGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCAT
GCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTT
CTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATCAGT
TGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATG
AATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATT
ATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTT
GCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGG
CCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTA
ATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCT
CTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCT
AAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTA
GTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCAT
ATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCT
TGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAA
TGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTT
GTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTT
TTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAAT
GGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384303 ⟹ NP_001371232

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,413,524 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,798,109 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTT
AAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAA
GTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAA
GCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTG
ATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAA
CATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACT
GCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGA
ACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGCTGTGTTAGACTTC
TGGCCCAGCTCTGTCGTGGTGCCCAACCTGAAGCTCTGCTCCAAGCCGCAAGGAGGACCGTCCTCCAGGTTGCTTCCTTTTGACCCACGCCGCCCCTGTCGCAGCCTCTTGTTGTTGTTCTGTTGTTG
CTGTGCCTCCTTCCTGCTCTCGGTTGCTGACCTCCAGGTGTCCAGACCAAATCAAAAGATAGAACTGAATTTTTCAGGTAATCAAAATGTGTCCCTGTAAACATGAAAATGTTTCCTAACCAGTGTGG
ATGAAAACTCATTCTAAAATGTTTTACACAGTATCCTTCATCTGAAAGCTATTATCCAGAATACACCTGATCAACTTTTCATGGTGATGAACTGTCAGCATTTACTGTTCTTTTGGCTGTTACCACAA
TAAGAAAAGAGAGATGAACTGTTAACATTTTTGCCTCCAGAAACTTAAATTCTAGAAAAGATTAATATTCTCATGTTTTATCCCTTTGTGTACCTCTGATAATAAACTAATTTTATGATTCAAA

hide sequence

RefSeq Acc Id:

NM_001384304 ⟹ NP_001371233

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATA
AATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGA
AGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATG
GCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCA
TTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTAT
CTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATC
ACAACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAA
GCATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGT
GCACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTC
TCTTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGAC
ATTTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAA
AGCCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTA
GGATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTAT
TTTCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTA
GCGTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACC
AAGTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGT
AGCTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAAC
AGTTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384305 ⟹ NP_001371234

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGTCTGTCAGCA
CTGCCTTCAAAATGCACCCAGAATAGATTCACAATTCTACCATTTCTCTCAACCGCCACTGTCACCACCTTGGTCCAGGCCCCCATCATCTGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAA
ATGATCATCCGTATGCTGATCATTTTGAATAGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGCCAGAAGGAAATATC
AGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAA
ATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAA
ATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATAT
CTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAG
GGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGT
CTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCAT
TCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTC
CCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGG
GTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATAT
CATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGA
TCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAA
TAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAA
GTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACT
GTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTAT
AATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384306 ⟹ NP_001371235

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTT
AAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAA
GTTTAATAAAGAACACCAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACT
CTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAG
GAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGA
GAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGA
CGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAACTGC
TTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTTCAC
TCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTCAAC
CCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTATTT
TCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGATTAC
ATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTCTGT
AATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAATTT
TTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTGTCA
TGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAAATT
TCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATGTCT
TCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAATAAA
ATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384307 ⟹ NP_001371236

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGTAACGGCCC
CGCTGCTGCCGTCGTCCCCCTCAGCCGGTTACCCTGTTACAGCCCCAGCTCTGGGCCCTTCCGGACCCTCCTGCTACGCTCTTTCTGGGCTTCCAGTATCGCCGGTCACTCAGTCCTCGCCCCTGCCT
GCCTCGCTGGCGCCCCGCCGTTTCCTCCTCGCGGCACAGTTTGCCAAGGAACAGCTACCCCGGCTCGGCAGTGACCGGGCGCCCCGGCGACACACGTACTCTCAGGCCCGCTGGGCAGGGGGACGGCC
TGGGCCGAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGAT
GGATCTGTTTGTTTCAATCTGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTC
ATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTG
AAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAG
GAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAA
CAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCAT
TACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCAC
AAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTT
TGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGACATTT
GTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCC
TGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTAGGAT
TTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTC
CAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGT
ATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGT
ATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCT
TTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTT
CTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384308 ⟹ NP_001371237

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCA
AAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATC
TGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAG
GCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATG
AGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGAC
AGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGA
CAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAACTGCTTCACTTGG
CGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTTCACTCTGTGGCT
GGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTCAACCCTCTACCT
TAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTATTTTCAAAATAG
CAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGATTACATTATAAGG
GATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTCTGTAATATTTGA
TGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAATTTTTTTCACAT
GAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTGTCATGTAAAAGC
AAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAAATTTCTGTTTGG
TTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATGTCTTCCACTTTT
CCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAATAAAATAGTTCTC
ATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384309 ⟹ NP_001371238

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCA
AAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATATGAGGAGATTGTGGACTGCCTAATATATTTCATCAGAAGAGAAGGCTGGAGAATTAAGCAGATGCAGCAAA
AAGCAGAAACTGACTTCAAAAAAAACCCTCTCAGTAGAGAAAGTGATATTAGATTCCTATTGCAAAGGATCTAATGCCAGTTAAATTCTCTTTTGCTTTCTTGATAAAACAGGAGAATTGAGAATTAA
ATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAA
TCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAA
AACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACT
TAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAA
GGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGA
ATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGC
AGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGC
TGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCC
TCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGA
TTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCT
GTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCT
CAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTAT
TGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCAT
AACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGG
GAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTT
TTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384310 ⟹ NP_001371239

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAAGACCAA
AACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAA
TTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCT
CAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTAC
AGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAAC
TACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCA
GAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGT
GTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAG
AAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCT
GTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTC
TCCCTCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGAC
TGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGA
GTCTGTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTA
ATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATA
TTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATT
CCATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTT
TAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGT
CCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384311 ⟹ NP_001371240

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGC
TTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCT
TCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGA
ATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGC
CAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAA
AAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGCATTACTAACTGCTTCACTTGGCGT
GCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGCACAAGAGTTCACTCTGTGGCTGGA
CTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTCTTTGAAGTCAACCCTCTACCTTAA
ACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGACATTTGTAGTTATTTTCAAAATAGCAG
CTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAGCCTGGGGATTACATTATAAGGGAT
GACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTAGGATTTAATTCTGTAATATTTGATGC
TGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTTTCCAATAAATTTTTTTCACATGAA
ATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGCGTATGTCTGTCATGTAAAAGCAAA
TCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACCAAGTATGAGAAATTTCTGTTTGGTTG
TAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAGCTTTCCATGTCTTCCACTTTTCCT
GTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAGTTCTCCAATAAAATAGTTCTCATT
CCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384312 ⟹ NP_001371241

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGTCTGTCAGCA
CTGCCTTCAAAATGCACCCAGAATAGATTCACAATTCTACCATTTCTCTCAACCGCCACTGTCACCACCTTGGTCCAGGCCCCCATCATCTGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAA
ATGATCATCCGTATGCTGATCATTTTGAATAGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGC
TCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATT
TGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCT
AGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCAC
AACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAACAAAGC
ATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGCAGTGC
ACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAACCTCTC
TTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACAGACAT
TTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTCAAAAG
CCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAATTTAGG
ATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCCTATTT
TCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATCTTAGC
GTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTTACCAA
GTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCTTGTAG
CTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCTAACAG
TTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_001384313 ⟹ NP_001371242

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCA
AAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTC
ATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTC
AGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCT
ATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAG
GCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTC
TATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATT
ATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGGTCTGTATTTCAGGGGCCCAGACAGTTTAAGATTCCAAAGTTAATAGAGAGAGGGTGTGAATTAATCATGGATGCGCCCCCTCTGTAAC
AAAGCATTACTAACTGCTTCACTTGGCGTGCTGCACTAAATAATTATGTTGTCTAATAGAGGGCACAGAAAGGGAGTGGTTTGAAGGAAAAACAGAAGCAGCTCAAACTAGAAATGTTCATCTGTTGC
AGTGCACAAGAGTTCACTCTGTGGCTGGACTGGTTTATCTGGAAATGACCATTCTCTAAGAGAGCACAGCTACAGTGCTAAGGGACTTTTTCCCTGTGCTGAAAAGATTGCATTGTGTTACGTGAAAC
CTCTCTTTGAAGTCAACCCTCTACCTTAAACTGTTGATTAAAAGGCTACTTCCCTAAAAACCTACTCAGTGCATCCGTTCAGGGCCTTTGTATTCTCCCTCACCATTTTGGCCAGGAATTACCACACA
GACATTTGTAGTTATTTTCAAAATAGCAGCTTTTCCCAGATAATGTTCCTGGGTAGTAGGGAAGGAAAAGGAATTAAAATAATTAAAGAGATGACTGGATTGATTTTCCTCAACAGCACTTGGTTGTC
AAAAGCCTGGGGATTACATTATAAGGGATGACTTGGGAGAAGGCATTGATATCATATTAAGAATTCTCCTGCATATCTTACATTAGCTAGTTTGAGTCTGTATAGACATAAACATAAATGGAATTAAT
TTAGGATTTAATTCTGTAATATTTGATGCTGAAACACGAGTATTTTCTATGATCTTGAAGTAAGTAAATATCAGGTTCGTTTCCTCCACGTTTTAATCTCAGTTATTTCTTCTGTTGTTAAAATTCCC
TATTTTCCAATAAATTTTTTTCACATGAAATTAATATGTGATCTACAGAAAATAATGAGCAACCTCAATTTTCACTCTTGTATACCAAAGTGATATTATTGGGCCTTTTAGGTAATATTGTATTCATC
TTAGCGTATGTCTGTCATGTAAAAGCAAATCTGTTTTCATGTATGTATCTAAGTTGTTCATGTTTTTATATCTATACATAAAACCAAAACAAATTCCATAACTATTTTCTTTGATACAAAAAGCACTT
ACCAAGTATGAGAAATTTCTGTTTGGTTGTAGGCATTTAGTGGAGGAAAACTGTTTTGTGGACCAAAACATGTTATTTCTTTAACATTAATGTTTTAGGGAGTGGTATTTTTAGTGATTCTTTCCCCT
TGTAGCTTTCCATGTCTTCCACTTTTCCTGTTTGGGAAAGTACTGCTGTTATAATGGAGGAGGTCCTACTTTATGTTAAAACAAAGAAAAGTGGTCCTTTTGGTAAGCTTTCTGTCAAGTCCAGATCT
AACAGTTCTCCAATAAAATAGTTCTCATTCCAGAGAGCAGATGAATATA

hide sequence

RefSeq Acc Id:

NM_152505 ⟹ NP_689718

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI
GRCh37	21	40,777,770 - 40,817,676 (-)	NCBI
Build 36	21	39,699,640 - 39,737,998 (-)	NCBI Archive
Celera	21	25,975,464 - 26,013,823 (-)	RGD
HuRef	21	26,246,616 - 26,285,006 (-)	ENTREZGENE
CHM1_1	21	40,338,935 - 40,377,266 (-)	NCBI
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

Sequence:

show sequence

GGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCA
AAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTC
ATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTC
AGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAG
CATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGAC
TTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGGCCAGAAGGAAATATC
AGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAA
ATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAA
ATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATAT
CTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAAC
AACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAA
AAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATT
CACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACT
GTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGAC
CAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCAT
GCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTT
CAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCC
AGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCC
TTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAA
TAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAATGCTGCTTATGTGCCTTGCATCTTATTTTTGAAATGTGTGAGAGAGGGAGTGTATGTATGTGTGTGTTTTAGTACTTAA
TTGACTTTCGATAATTAAATTTTTGTTTGATTGCTAA

hide sequence

RefSeq Acc Id:

XM_011529458 ⟹ XP_011527760

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

ACAGCCCCAGCTCTGGGCCCTTCCGGACCCTCCTGCTACGCTCTTTCTGGGCTTCCAGTATCGC
CGGTCACTCAGTCCTCGCCCCTGCCTGCCTCGCTGGCGCCCCGCCGTTTCCTCCTCGCGGCACAGTTTGCCAAGGAACAGCTACCCCGGCTCGGCAGTGACCGGGCGCCCCGGCGACACACGTACTCT
CAGGCCCGCTGGGCAGGGGGACGGCCTGGGCCGAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTTAAAATATATTCTTTCTTTA
AAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAG
TGAGGAGATTGTGGACTGCCTAATATATTTCATCAGAAGAGAAGGCTGGAGAATTAAGCAGATGCAGCAAAAAGCAGAAACTGACTTCAAAAAAAACCCTCTCAGTAGAGAAAGTGATATTAGATTCC
TATTGCAAAGGATCTAATGCCAGTTAAATTCTCTTTTGCTTTCTTGATAAAACAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTG
CTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGA
TTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTA
TTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGTTAACAGGTGGCCTTGTTACAGAGTACCACAATATTTGGATTTC
ACTGGCTTCTTGCCTTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGAGGATGGTCTCCAAGTCTGGCCAGAAGGAAATATCAGTTGAAAA
AAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAG
CTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCT
AAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGC
ACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGT
TGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGT
GAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTAT
GAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATA
AACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAG
AAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAA
TGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGC
CAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAA
GTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAG
TAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTT
AAATATAATCAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529459 ⟹ XP_011527761

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

CGCGCGGGTTTCCATGGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGG
AGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATAC
TACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAAT
CCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACA
ATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTAT
GATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGT
TAACAGGTGGCCTTGTTACAGAGTACCACAATATTTGGATTTCACTGGCTTCTTGCCTTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGA
GGATGGTCTCCAAGTCTGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTC
TCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGG
AAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAG
AAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGAC
GCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGT
GGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAA
AATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAA
AAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGA
GAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAG
ATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAA
GCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGA
CAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAAT
CAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATT
AAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529460 ⟹ XP_011527762

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

CGCGCGGGTTTCCATGGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCAT
TTTGAATACCTTCAGCCATGCTTCTGCCACTGCCTCTGCAGGAAAGCCACCTGCTTTAAAAAAAAGTCTTCATGGAGTGCTTATGAGAGGGTCGGCTGTTTTCTCCAGCTCATTTTTCCAAAGCAAAC
AATCCCACCAGCTATCTCAGGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTT
CAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGG
TTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACG
GAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAA
ATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGTTAACAGGTGGCCTTGTTACAGAGTACCACAATATTTGGATTTCACTGGCTTC
TTGCCTTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGAGGATGGTCTCCAAGTCTGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACAC
CTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGC
ATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAG
AATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAA
ACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCA
GAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAA
ATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCA
GGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAA
AGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATT
TTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGA
TGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATG
CCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGAT
ACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTC
GCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAAT
CAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529461 ⟹ XP_011527763

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

AGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGA
TCATCCGTATGCTGATCATTTTGAATACCTTCAGCCATGCTTCTGCCACTGCCTCTGCAGGAAAGCCACCTGCTTTAAAAAAAAGTCTTCATGGAGTGCTTATGAGAGGGTCGGCTGTTTTCTCCAGC
TCATTTTTCCAAAGCAAACAATCCCACCAGCTATCTCAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATC
AGACATCTTAGGGAAGTTTAATAAAGAACACCAGTGAGGAGATTGTGGACTGCCTAATATATTTCATCAGAAGAGAAGGCTGGAGAATTAAGCAGATGCAGCAAAAAGCAGAAACTGACTTCAAAAAA
AACCCTCTCAGTAGAGAAAGTGATATTAGATTCCTATTGCAAAGGATCTAATGCCAGTTAAATTCTCTTTTGCTTTCTTGATAAAACAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAA
GACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGT
CTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCA
GAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGTTAACAGGTG
GCCTTGTTACAGAGTACCACAATATTTGGATTTCACTGGCTTCTTGCCTTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGAGGATGGTCT
CCAAGTCTGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGG
CTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGA
GAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACA
GCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGAC
AAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAA
ACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCC
AAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACT
GAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGG
AAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAG
TAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAA
AACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTA
TGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTG
GTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCG
TCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529462 ⟹ XP_011527764

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

GCAGTCGTGGGAACAGCGCGGAGCAGGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCT
TATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTT
TTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTT
TTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTA
ATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGTTAACAGGTGGCCTTGTTACAGAGTACCACAATATTTGGATTTCACT
GGCTTCTTGCCTTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGAGGATGGTCTCCAAGTCTGGCCAGAAGGAAATATCAGTTGAAAAAAA
GCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTG
ATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAA
CATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACT
GCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGA
ACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAG
CTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAG
ACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAAC
TACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAA
AACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGG
TGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAG
CCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTG
AAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAA
GGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAA
TATAATCAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529463 ⟹ XP_011527765

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

CCCGGCTCGGCAGTGACCGGGCGCCCCGGCGACACACGTACTCTCAGGCCCGCTGGGCAGGGGG
ACGGCCTGGGCCGAGGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTT
TATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTT
TGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACA
GTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTAT
TTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGTTAACAGGTGGCCTTGTTACAGAGTACCACAATATTTGGATTTCACTGGCTTCTTGCC
TTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGAGGATGGTCTCCAAGTCTGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGA
ATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCAT
AAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGA
AGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTT
CTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCC
TTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAA
AAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAA
CCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAA
GAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGT
GAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACA
CACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGC
AACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAAC
TTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATC
CCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATA
TCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529464 ⟹ XP_011527766

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

CGCGCGGGTTTCCATGGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGG
AGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGT
GAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTT
TGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCC
AGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTT
CAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGTTAACAGGTGGCCTTGTTACAGAGTACCACAA
TATTTGGATTTCACTGGCTTCTTGCCTTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGAGGATGGTCTCCAAGTCTGGCCAGAAGGAAAT
ATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAA
AAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCT
CAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGA
TATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAA
AACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAG
GAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCC
ATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTC
ACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAA
GACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAG
CATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTG
CTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCT
TCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGA
GCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAA
AAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529465 ⟹ XP_011527767

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

TGGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGACCAAAA
CCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATT
AAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGC
GTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAG
TTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAA
TCTCCCAATCTAAAGTTAACAGGTGGCCTTGTTACAGAGTACCACAATATTTGGATTTCACTGGCTTCTTGCCTTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTA
TCTCAGCACCCCAAGAGGATGGTCTCCAAGTCTGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTAT
GGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGC
ATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTA
TCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTAT
CACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTA
CCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCA
AAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAA
CATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAG
TCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGA
GAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACA
TTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGG
AGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTC
TTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAAC
TGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529466 ⟹ XP_011527768

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

GGGAACAGCGCGGAGCAGGTAACGGCCCCGCTGCTGCCGTCGTCCCCCTCAGCCGGTTACCCTGTTACAGCCCCAGCTCTGGGCCCTTCCGGACCCTCCTGCTACGCTCTTTCTGGGCTTCCAGTATC
GCCGGTCACTCAGTCCTCGCCCCTGCCTGCCTCGCTGGCGCCCCGCCGTTTCCTCCTCGCGGCACAGTTTGCCAAGGAACAGCTACCCCGGCTCGGCAGTGACCGGGCGCCCCGGCGACACACGTACT
CTCAGGCCCGCTGGGCAGGGGGACGGCCTGGGCCGAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAG
ACATCTTAGGGAAGTTTAATAAAGAACACCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTC
TTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTT
CCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAG
CCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGTTAACAGGTGGCCTTGTTACAGAGTACCACAATATTTGGATTTCACTGGCTTCTTGCCTTTCATCTC
AGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGAGGATGGTCTCCAAGTCTGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCAC
TCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAA
GCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAA
TTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACA
AAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGG
CAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTA
TAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAAT
CAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCT
AAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGA
GCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCA
AAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGG
TACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGA
TAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTC
CCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGC
ATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529467 ⟹ XP_011527769

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

CGCGCGGGTTTCCATGGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGG
AGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATAC
TACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATCAGACATCTTAGGGAAGTTTAATAAAGAACACCAGTGAGGAGATTGTGGACTGCCTAATATATTT
CATCAGAAGAGAAGGCTGGAGAATTAAGCAGATGCAGCAAAAAGCAGAAACTGACTTCAAAAAAAACCCTCTCAGTAGAGAAAGTGATATTAGATTCCTATTGCAAAGGATCTAATGCCAGTTAAATT
CTCTTTTGCTTTCTTGATAAAACAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTTTACTTTTCTTTTATTAGG
TTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACG
GAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAA
ATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGTTAACAGGTGGCCTTGTTACAGAGTACCACAATATTTGGATTTCACTGGCTTC
TTGCCTTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGAGGATGGTCTCCAAGTCTGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACAC
CTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGC
ATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAG
AATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAA
ACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCA
GAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAA
ATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCA
GGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAA
AGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATT
TTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGA
TGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATG
CCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGAT
ACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTC
GCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAAT
CAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529468 ⟹ XP_011527770

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

CGCGCGGGTTTCCATGGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGG
AGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCATTTTGAATAGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTCAGAAGATGGAT
CTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAGCATGCAAGAGA
AGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGACTTTCTCTGTGA
TTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGTTAACAGGTGGCCTTGTTACAGAGTAC
CACAATATTTGGATTTCACTGGCTTCTTGCCTTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGAGGATGGTCTCCAAGTCTGGCCAGAAG
GAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGG
ACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATC
TACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACT
AAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTT
GGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAAC
TTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATT
TTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAAT
TCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAA
AAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAA
AGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCT
TCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTA
AGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCA
GAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAA
AAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_011529470 ⟹ XP_011527772

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

TGGGAACAGCGCGGAGCAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAAGACCTC
AGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGTTGTTTGCTATGTCTTTGGCTGATCTAACAAAAACAAATATAGATGAGCATTTCTTCGGCGTGGCATTAGAAAACAATAGGAGGTCTGCAG
CATGCAAGAGAAGCCCAGGCACAGGCGATTTTTCACGGAACAGTAATGCTTCCAATAAGAGTGTTGATTATAGCAGATCTCAGTGCTCCTGTGGAAGTTTAAGTTCTCAGTATGATTATTCAGAAGAC
TTTCTCTGTGATTGTTCAGAAAAGGCTATTAATAGAAATTATTTAAAGCAGCCTGTGGTAAAAGAAAAGGAGAAGAAAAAGTATAATGTTTCTAAAATCTCCCAATCTAAAGTTAACAGGTGGCCTTG
TTACAGAGTACCACAATATTTGGATTTCACTGGCTTCTTGCCTTTCATCTCAGCTGAAGAATCAGTGTTTGAATTGCCAGTGAAATGTAAATACCTATCTCAGCACCCCAAGAGGATGGTCTCCAAGT
CTGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGAGATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCAT
AAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCAGCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTC
ACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAAGAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGT
TACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTATCTATTATCACAACAAAAATGGACGCAAATGACAAAAAA
ATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCAGACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCT
TCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGGACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAG
ACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCAACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATA
AATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACATTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACA
AAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATCCTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAG
AAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAAAGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTG
CATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGAGGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCC
CTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAGGCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTG
CAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCTAAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCT
ACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_017028274 ⟹ XP_016883763

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

Sequence:

show sequence

CGCGCGGGTTTCCATGGGGACGCGCCGGCGCTGCGGCGTTGGCGCAGTCGTGGGAACAGCGCGGAGCAGAGAAGCACCAAAAGAGGCAAACTGAGATGCAGACAAATGATCATCCGTATGCTGATCAT
TTTGAATAGTTTTTTAAAATATATTCTTTCTTTAAAAAGAGACCAAAACCTGTCAAAAAAATACTACCGTGGAAAGCTCATAAATACTACAGTGTGAAGAACCCTGTGCTTATCTTCAGTTTATCATC
AGACATCTTAGGGAAGTTTAATAAAGAACACCAGTGAGGAGATTGTGGACTGCCTAATATATTTCATCAGAAGAGAAGGCTGGAGAATTAAGCAGATGCAGCAAAAAGCAGAAACTGACTTCAAAAAA
AACCCTCTCAGTAGAGAAAGTGATATTAGATTCCTATTGCAAAGGATCTAATGCCAGTTAAATTCTCTTTTGCTTTCTTGATAAAACAGGAGAATTGAGAATTAAATGAAAAGGTAAATCCTTTTAAA
GACCTCAGAAGATGGATCTGTTTGTTTCAATCTGCTTTTGAGGCCAGAAGGAAATATCAGTTGAAAAAAAGCACACCTGGAATGCATCACTCTTTAATTCTCAAATCCATATGATTGCCCAAAGAAGA
GATGCTATGGCTCATCGAATACTCTCAGCAAGGCTTCATAAAATTAAAGGACTAAAAAATGAATTAGCTGATATGCATCATAAATTGGAAGCCATCCTTACAGAAAACCAATTTTTGAAACAACTTCA
GCTTAGGCATTTGAAAGCTATAGGAAAATATGAGAATTCACAAAATAATCTACCTCAAATTATGGCTAAACATCAGAATGAAGTAAAAAATTTAAGGCAACTACTTAGGAAATCCCAGGAAAAGGAAA
GAACTCTATCTAGGAAACTTAGAGAAACTGACAGCCAGTTACTGAAGACTAAAGATATCTTGCAGGCACTGCAGAAACTTTCTGAAGACAAAAACCTTGCAGAAAGGGAAGAACTCACTCATAAATTA
TCTATTATCACAACAAAAATGGACGCAAATGACAAAAAAATACAGAGCTTGGAAAAACAACTGAGGTTGAACTGCAGAGCCTTTAGCCGGCAGCTGGCTATTGAGACTCGGAAGACTTTAGCAGCTCA
GACAGCTACCAAGACTCTGCAGGTGGAAGTAAAACACCTTCAACAAAAACTTAAGGAAAAGGATCGTGAGCTTGAAATTAAAAACATCTATAGTCATCGAATACTTAAAAATTTACATGACACAGAGG
ACTATCCAAAAGTTTCTTCAACAAAATCAGTCCAAGCAGACAGAAAAATTTTGCCATTCACAAGTATGAGACACCAGGGAACCCAAAAATCAGATGTTCCACCTTTGACAACTAAGGGTAAAAAGGCA
ACAGGAAACATCGATCATAAAGAAAAATCAACTGAAATAAATCATGAAATTCCTCACTGTGTGAATAAACTACCAAAGCAAGAGGATTCTAAGAGAAAATATGAAGATTTATCAGGGGAAGAGAAACA
TTTGGAAGTCCAAATACTGCTGGAGAATACTGGAAGACAAAAAGACAAAAAAGAAGACCAAGAAAAGAAAAACATTTTTGTGAAAGAAGAGCAAGAACTACCACCAAAAATAATTGAAGTTATTCATC
CTGAAAGAGAAAGCAATCAAGAAGATGTTCTAGTAAGAGAAAAGTTTAAAAGAAGCATGCAGAGAAATGGTGTGGATGACACACTTGGCAAAGGCACTGCTCCCTACACGAAAGGCCCCCTCAGACAA
AGAAGACATTACTCATTCACAGAAGCAACTGAAAACCTGCATCATGGGCTTCCTGCTTCAGGGGGGCCAGCCAATGCCGGCAACATGAGGTACAGTCATAGTACAGGCAAGCATCTCAGTAACAGAGA
GGAAATGGAGCTAGAGCATTCTGACAGTGGGTATGAGCCCTCATTTGGTAAGTCTTCCAGAATAAAAGTGAAGGATACAACTTTCAGAGATAAGAAAAGCAGTCTCATGGAAGAACTCTTTGGATCAG
GCTATGTCTTGAAAACTGACCAATCAAGTCCTGGTGTTGCAAAAGGCTCAGAGGAGCCTTTGCAAAGTAAGGAGTCGCATCCCCTGCCTCCCAGTCAGGCCTCCACCAGCCATGCTTTCGGAGACTCT
AAAGTAACTGTGGTAAATTCTATTAAGCCATCGTCACCTACAGAAGGAAAAAGAAAAATAATTATTTAAATATAATCAATATCCTAATGCATTCTGGTTTGATATAA

hide sequence

RefSeq Acc Id:

XM_047440684 ⟹ XP_047296640

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440685 ⟹ XP_047296641

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440686 ⟹ XP_047296642

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440687 ⟹ XP_047296643

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440688 ⟹ XP_047296644

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440689 ⟹ XP_047296645

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440690 ⟹ XP_047296646

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440691 ⟹ XP_047296647

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440692 ⟹ XP_047296648

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440693 ⟹ XP_047296649

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440694 ⟹ XP_047296650

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440695 ⟹ XP_047296651

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440696 ⟹ XP_047296652

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440697 ⟹ XP_047296653

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,405,728 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_047440698 ⟹ XP_047296654

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,421,558 - 39,445,778 (-)	NCBI

RefSeq Acc Id:

XM_054324335 ⟹ XP_054180310

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324336 ⟹ XP_054180311

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324337 ⟹ XP_054180312

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324338 ⟹ XP_054180313

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324339 ⟹ XP_054180314

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324340 ⟹ XP_054180315

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324341 ⟹ XP_054180316

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324342 ⟹ XP_054180317

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324343 ⟹ XP_054180318

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324344 ⟹ XP_054180319

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324345 ⟹ XP_054180320

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324346 ⟹ XP_054180321

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324347 ⟹ XP_054180322

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324348 ⟹ XP_054180323

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324349 ⟹ XP_054180324

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324350 ⟹ XP_054180325

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324351 ⟹ XP_054180326

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324352 ⟹ XP_054180327

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324353 ⟹ XP_054180328

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324354 ⟹ XP_054180329

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324355 ⟹ XP_054180330

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324356 ⟹ XP_054180331

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324357 ⟹ XP_054180332

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324358 ⟹ XP_054180333

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324359 ⟹ XP_054180334

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324360 ⟹ XP_054180335

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,790,313 - 37,830,401 (-)	NCBI

RefSeq Acc Id:

XM_054324361 ⟹ XP_054180336

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	21	37,806,160 - 37,830,401 (-)	NCBI


Protein RefSeqs	NP_001371214	(Get FASTA)	NCBI Sequence Viewer
	NP_001371215	(Get FASTA)	NCBI Sequence Viewer
	NP_001371216	(Get FASTA)	NCBI Sequence Viewer
	NP_001371217	(Get FASTA)	NCBI Sequence Viewer
	NP_001371218	(Get FASTA)	NCBI Sequence Viewer
	NP_001371220	(Get FASTA)	NCBI Sequence Viewer
	NP_001371221	(Get FASTA)	NCBI Sequence Viewer
	NP_001371222	(Get FASTA)	NCBI Sequence Viewer
	NP_001371223	(Get FASTA)	NCBI Sequence Viewer
	NP_001371224	(Get FASTA)	NCBI Sequence Viewer
	NP_001371225	(Get FASTA)	NCBI Sequence Viewer
	NP_001371226	(Get FASTA)	NCBI Sequence Viewer
	NP_001371227	(Get FASTA)	NCBI Sequence Viewer
	NP_001371228	(Get FASTA)	NCBI Sequence Viewer
	NP_001371229	(Get FASTA)	NCBI Sequence Viewer
	NP_001371230	(Get FASTA)	NCBI Sequence Viewer
	NP_001371231	(Get FASTA)	NCBI Sequence Viewer
	NP_001371232	(Get FASTA)	NCBI Sequence Viewer
	NP_001371233	(Get FASTA)	NCBI Sequence Viewer
	NP_001371234	(Get FASTA)	NCBI Sequence Viewer
	NP_001371235	(Get FASTA)	NCBI Sequence Viewer
	NP_001371236	(Get FASTA)	NCBI Sequence Viewer
	NP_001371237	(Get FASTA)	NCBI Sequence Viewer
	NP_001371238	(Get FASTA)	NCBI Sequence Viewer
	NP_001371239	(Get FASTA)	NCBI Sequence Viewer
	NP_001371240	(Get FASTA)	NCBI Sequence Viewer
	NP_001371241	(Get FASTA)	NCBI Sequence Viewer
	NP_001371242	(Get FASTA)	NCBI Sequence Viewer
	NP_689718	(Get FASTA)	NCBI Sequence Viewer
	XP_011527760	(Get FASTA)	NCBI Sequence Viewer
	XP_011527761	(Get FASTA)	NCBI Sequence Viewer
	XP_011527762	(Get FASTA)	NCBI Sequence Viewer
	XP_011527763	(Get FASTA)	NCBI Sequence Viewer
	XP_011527764	(Get FASTA)	NCBI Sequence Viewer
	XP_011527765	(Get FASTA)	NCBI Sequence Viewer
	XP_011527766	(Get FASTA)	NCBI Sequence Viewer
	XP_011527767	(Get FASTA)	NCBI Sequence Viewer
	XP_011527768	(Get FASTA)	NCBI Sequence Viewer
	XP_011527769	(Get FASTA)	NCBI Sequence Viewer
	XP_011527770	(Get FASTA)	NCBI Sequence Viewer
	XP_011527772	(Get FASTA)	NCBI Sequence Viewer
	XP_016883763	(Get FASTA)	NCBI Sequence Viewer
	XP_047296640	(Get FASTA)	NCBI Sequence Viewer
	XP_047296641	(Get FASTA)	NCBI Sequence Viewer
	XP_047296642	(Get FASTA)	NCBI Sequence Viewer
	XP_047296643	(Get FASTA)	NCBI Sequence Viewer
	XP_047296644	(Get FASTA)	NCBI Sequence Viewer
	XP_047296645	(Get FASTA)	NCBI Sequence Viewer
	XP_047296646	(Get FASTA)	NCBI Sequence Viewer
	XP_047296647	(Get FASTA)	NCBI Sequence Viewer
	XP_047296648	(Get FASTA)	NCBI Sequence Viewer
	XP_047296649	(Get FASTA)	NCBI Sequence Viewer
	XP_047296650	(Get FASTA)	NCBI Sequence Viewer
	XP_047296651	(Get FASTA)	NCBI Sequence Viewer
	XP_047296652	(Get FASTA)	NCBI Sequence Viewer
	XP_047296653	(Get FASTA)	NCBI Sequence Viewer
	XP_047296654	(Get FASTA)	NCBI Sequence Viewer
	XP_054180310	(Get FASTA)	NCBI Sequence Viewer
	XP_054180311	(Get FASTA)	NCBI Sequence Viewer
	XP_054180312	(Get FASTA)	NCBI Sequence Viewer
	XP_054180313	(Get FASTA)	NCBI Sequence Viewer
	XP_054180314	(Get FASTA)	NCBI Sequence Viewer
	XP_054180315	(Get FASTA)	NCBI Sequence Viewer
	XP_054180316	(Get FASTA)	NCBI Sequence Viewer
	XP_054180317	(Get FASTA)	NCBI Sequence Viewer
	XP_054180318	(Get FASTA)	NCBI Sequence Viewer
	XP_054180319	(Get FASTA)	NCBI Sequence Viewer
	XP_054180320	(Get FASTA)	NCBI Sequence Viewer
	XP_054180321	(Get FASTA)	NCBI Sequence Viewer
	XP_054180322	(Get FASTA)	NCBI Sequence Viewer
	XP_054180323	(Get FASTA)	NCBI Sequence Viewer
	XP_054180324	(Get FASTA)	NCBI Sequence Viewer
	XP_054180325	(Get FASTA)	NCBI Sequence Viewer
	XP_054180326	(Get FASTA)	NCBI Sequence Viewer
	XP_054180327	(Get FASTA)	NCBI Sequence Viewer
	XP_054180328	(Get FASTA)	NCBI Sequence Viewer
	XP_054180329	(Get FASTA)	NCBI Sequence Viewer
	XP_054180330	(Get FASTA)	NCBI Sequence Viewer
	XP_054180331	(Get FASTA)	NCBI Sequence Viewer
	XP_054180332	(Get FASTA)	NCBI Sequence Viewer
	XP_054180333	(Get FASTA)	NCBI Sequence Viewer
	XP_054180334	(Get FASTA)	NCBI Sequence Viewer
	XP_054180335	(Get FASTA)	NCBI Sequence Viewer
	XP_054180336	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAD12066	(Get FASTA)	NCBI Sequence Viewer
	AAH31059	(Get FASTA)	NCBI Sequence Viewer
	AAH43006	(Get FASTA)	NCBI Sequence Viewer
	CAB90455	(Get FASTA)	NCBI Sequence Viewer
	EAX09641	(Get FASTA)	NCBI Sequence Viewer
	EAX09642	(Get FASTA)	NCBI Sequence Viewer
	EAX09643	(Get FASTA)	NCBI Sequence Viewer
	EAX09644	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000288350
	ENSP00000288350.3
	ENSP00000351008
	ENSP00000351008.2
	ENSP00000370046
	ENSP00000370046.2
	ENSP00000475187
GenBank Protein	O95447	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_689718 ⟸ NM_152505
- Peptide Label:	isoform a
- UniProtKB:	Q3ZCT0 (UniProtKB/Swiss-Prot), O95447 (UniProtKB/Swiss-Prot), D3DSI0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSLADLTKTNIDEHFFGVALENNRRSAACKRSPGTGDFSRNSNASNKSVDYSRSQCSCGSLSSQYDYSEDFLCDCSEKAINRNYLKQPVVKEKEKKKYNVSKISQSKGQKEISVEKKHTWNASLFNSQ IHMIAQRRDAMAHRILSARLHKIKGLKNELADMHHKLEAILTENQFLKQLQLRHLKAIGKYENSQNNLPQIMAKHQNEVKNLRQLLRKSQEKERTLSRKLRETDSQLLKTKDILQALQKLSEDKNLAE REELTHKLSIITTKMDANDKKIQSLEKQLRLNCRAFSRQLAIETRKTLAAQTATKTLQVEVKHLQQKLKEKDRELEIKNIYSHRILKNLHDTEDYPKVSSTKSVQADRKILPFTSMRHQGTQKSDVPP LTTKGKKATGNIDHKEKSTEINHEIPHCVNKLPKQEDSKRKYEDLSGEEKHLEVQILLENTGRQKDKKEDQEKKNIFVKEEQELPPKIIEVIHPERESNQEDVLVREKFKRSMQRNGVDDTLGKGTAP YTKGPLRQRRHYSFTEATENLHHGLPASGGPANAGNMRYSHSTGKHLSNREEMELEHSDSGYEPSFGKSSRIKVKDTTFRDKKSSLMEELFGSGYVLKTDQSSPGVAKGSEEPLQSKESHPLPPSQAS TSHAFGDSKVTVVNSIKPSSPTEGKRKIII hide sequence

RefSeq Acc Id:

XP_011527770 ⟸ XM_011529468

- Peptide Label:

isoform X1

- Sequence:

show sequence

MSLADLTKTNIDEHFFGVALENNRRSAACKRSPGTGDFSRNSNASNKSVDYSRSQCSCGSLSSQ
YDYSEDFLCDCSEKAINRNYLKQPVVKEKEKKKYNVSKISQSKVNRWPCYRVPQYLDFTGFLPFISAEESVFELPVKCKYLSQHPKRMVSKSGQKEISVEKKHTWNASLFNSQIHMIAQRRDAMAHRI
LSARLHKIKGLKNELADMHHKLEAILTENQFLKQLQLRHLKAIGKYENSQNNLPQIMAKHQNEVKNLRQLLRKSQEKERTLSRKLRETDSQLLKTKDILQALQKLSEDKNLAEREELTHKLSIITTKM
DANDKKIQSLEKQLRLNCRAFSRQLAIETRKTLAAQTATKTLQVEVKHLQQKLKEKDRELEIKNIYSHRILKNLHDTEDYPKVSSTKSVQADRKILPFTSMRHQGTQKSDVPPLTTKGKKATGNIDHK
EKSTEINHEIPHCVNKLPKQEDSKRKYEDLSGEEKHLEVQILLENTGRQKDKKEDQEKKNIFVKEEQELPPKIIEVIHPERESNQEDVLVREKFKRSMQRNGVDDTLGKGTAPYTKGPLRQRRHYSFT
EATENLHHGLPASGGPANAGNMRYSHSTGKHLSNREEMELEHSDSGYEPSFGKSSRIKVKDTTFRDKKSSLMEELFGSGYVLKTDQSSPGVAKGSEEPLQSKESHPLPPSQASTSHAFGDSKVTVVNS
IKPSSPTEGKRKIII

hide sequence

RefSeq Acc Id:

XP_011527766 ⟸ XM_011529464

- Peptide Label:

isoform X1

- Sequence:

show sequence

MSLADLTKTNIDEHFFGVALENNRRSAACKRSPGTGDFSRNSNASNKSVDYSRSQCSCGSLSSQ
YDYSEDFLCDCSEKAINRNYLKQPVVKEKEKKKYNVSKISQSKVNRWPCYRVPQYLDFTGFLPFISAEESVFELPVKCKYLSQHPKRMVSKSGQKEISVEKKHTWNASLFNSQIHMIAQRRDAMAHRI
LSARLHKIKGLKNELADMHHKLEAILTENQFLKQLQLRHLKAIGKYENSQNNLPQIMAKHQNEVKNLRQLLRKSQEKERTLSRKLRETDSQLLKTKDILQALQKLSEDKNLAEREELTHKLSIITTKM
DANDKKIQSLEKQLRLNCRAFSRQLAIETRKTLAAQTATKTLQVEVKHLQQKLKEKDRELEIKNIYSHRILKNLHDTEDYPKVSSTKSVQADRKILPFTSMRHQGTQKSDVPPLTTKGKKATGNIDHK
EKSTEINHEIPHCVNKLPKQEDSKRKYEDLSGEEKHLEVQILLENTGRQKDKKEDQEKKNIFVKEEQELPPKIIEVIHPERESNQEDVLVREKFKRSMQRNGVDDTLGKGTAPYTKGPLRQRRHYSFT
EATENLHHGLPASGGPANAGNMRYSHSTGKHLSNREEMELEHSDSGYEPSFGKSSRIKVKDTTFRDKKSSLMEELFGSGYVLKTDQSSPGVAKGSEEPLQSKESHPLPPSQASTSHAFGDSKVTVVNS
IKPSSPTEGKRKIII

hide sequence

RefSeq Acc Id:

XP_011527761 ⟸ XM_011529459

- Peptide Label:

isoform X1

- Sequence:

show sequence

MSLADLTKTNIDEHFFGVALENNRRSAACKRSPGTGDFSRNSNASNKSVDYSRSQCSCGSLSSQ
YDYSEDFLCDCSEKAINRNYLKQPVVKEKEKKKYNVSKISQSKVNRWPCYRVPQYLDFTGFLPFISAEESVFELPVKCKYLSQHPKRMVSKSGQKEISVEKKHTWNASLFNSQIHMIAQRRDAMAHRI
LSARLHKIKGLKNELADMHHKLEAILTENQFLKQLQLRHLKAIGKYENSQNNLPQIMAKHQNEVKNLRQLLRKSQEKERTLSRKLRETDSQLLKTKDILQALQKLSEDKNLAEREELTHKLSIITTKM
DANDKKIQSLEKQLRLNCRAFSRQLAIETRKTLAAQTATKTLQVEVKHLQQKLKEKDRELEIKNIYSHRILKNLHDTEDYPKVSSTKSVQADRKILPFTSMRHQGTQKSDVPPLTTKGKKATGNIDHK
EKSTEINHEIPHCVNKLPKQEDSKRKYEDLSGEEKHLEVQILLENTGRQKDKKEDQEKKNIFVKEEQELPPKIIEVIHPERESNQEDVLVREKFKRSMQRNGVDDTLGKGTAPYTKGPLRQRRHYSFT
EATENLHHGLPASGGPANAGNMRYSHSTGKHLSNREEMELEHSDSGYEPSFGKSSRIKVKDTTFRDKKSSLMEELFGSGYVLKTDQSSPGVAKGSEEPLQSKESHPLPPSQASTSHAFGDSKVTVVNS
IKPSSPTEGKRKIII

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RefSeq Acc Id:

XP_011527769 ⟸ XM_011529467

- Peptide Label:

isoform X1

- Sequence:

show sequence

MSLADLTKTNIDEHFFGVALENNRRSAACKRSPGTGDFSRNSNASNKSVDYSRSQCSCGSLSSQ
YDYSEDFLCDCSEKAINRNYLKQPVVKEKEKKKYNVSKISQSKVNRWPCYRVPQYLDFTGFLPFISAEESVFELPVKCKYLSQHPKRMVSKSGQKEISVEKKHTWNASLFNSQIHMIAQRRDAMAHRI
LSARLHKIKGLKNELADMHHKLEAILTENQFLKQLQLRHLKAIGKYENSQNNLPQIMAKHQNEVKNLRQLLRKSQEKERTLSRKLRETDSQLLKTKDILQALQKLSEDKNLAEREELTHKLSIITTKM
DANDKKIQSLEKQLRLNCRAFSRQLAIETRKTLAAQTATKTLQVEVKHLQQKLKEKDRELEIKNIYSHRILKNLHDTEDYPKVSSTKSVQADRKILPFTSMRHQGTQKSDVPPLTTKGKKATGNIDHK
EKSTEINHEIPHCVNKLPKQEDSKRKYEDLSGEEKHLEVQILLENTGRQKDKKEDQEKKNIFVKEEQELPPKIIEVIHPERESNQEDVLVREKFKRSMQRNGVDDTLGKGTAPYTKGPLRQRRHYSFT
EATENLHHGLPASGGPANAGNMRYSHSTGKHLSNREEMELEHSDSGYEPSFGKSSRIKVKDTTFRDKKSSLMEELFGSGYVLKTDQSSPGVAKGSEEPLQSKESHPLPPSQASTSHAFGDSKVTVVNS
IKPSSPTEGKRKIII

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Protein Domains

Lebercilin

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-O95447-F1-model_v2	AlphaFold	O95447	1-670	view protein structure

RGD ID:

13602850

Promoter ID:

EPDNEW_H27609

Type:

initiation region

Name:

LCA5L_1

Description:

LCA5L, lebercilin like

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	21	39,445,748 - 39,445,808	EPDNEW

RGD ID:

6799477

Promoter ID:

HG_KWN:40914

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000288350, ENST00000380631, ENST00000380634, OTTHUMT00000141812, OTTHUMT00000141813, OTTHUMT00000141814, OTTHUMT00000141815, OTTHUMT00000141816, OTTHUMT00000141817, OTTHUMT00000141818, OTTHUMT00000141819, OTTHUMT00000141820, OTTHUMT00000141821, OTTHUMT00000141833, OTTHUMT00000141834, OTTHUMT00000141835, OTTHUMT00000157378, OTTHUMT00000157380, OTTHUMT00000157381, OTTHUMT00000194971, UC002YXV.1, UC002YXW.1, UC002YXX.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	21	39,739,431 - 39,739,931 (-)	MPROMDB

Database	Acc Id	Source(s)
COSMIC	LCA5L	COSMIC
Ensembl Genes	ENSG00000157578	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000288350	ENTREZGENE
	ENST00000288350.8	UniProtKB/Swiss-Prot
	ENST00000358268	ENTREZGENE
	ENST00000358268.6	UniProtKB/Swiss-Prot
	ENST00000380671	ENTREZGENE
	ENST00000380671.6	UniProtKB/Swiss-Prot
	ENST00000485895	ENTREZGENE
GTEx	ENSG00000157578	GTEx
HGNC ID	HGNC:1255	ENTREZGENE
Human Proteome Map	LCA5L	Human Proteome Map
InterPro	Lebercilin-like	UniProtKB/Swiss-Prot
	Lebercilin_dom	UniProtKB/Swiss-Prot
KEGG Report	hsa:150082	UniProtKB/Swiss-Prot
NCBI Gene	LCA5L	ENTREZGENE
PANTHER	LEBERCILIN-LIKE PROTEIN	UniProtKB/Swiss-Prot
	PTHR16650	UniProtKB/Swiss-Prot
Pfam	Lebercilin	UniProtKB/Swiss-Prot
PharmGKB	PA162393809	PharmGKB
UniProt	A0A1D5RMP5_HUMAN	UniProtKB/TrEMBL
	C9J198_HUMAN	UniProtKB/TrEMBL
	C9J293_HUMAN	UniProtKB/TrEMBL
	C9J5D2_HUMAN	UniProtKB/TrEMBL
	C9J9Z3_HUMAN	UniProtKB/TrEMBL
	C9JFB6_HUMAN	UniProtKB/TrEMBL
	C9JIJ8_HUMAN	UniProtKB/TrEMBL
	C9JRD7_HUMAN	UniProtKB/TrEMBL
	C9JYR0_HUMAN	UniProtKB/TrEMBL
	D3DSI0	ENTREZGENE
	LCA5L_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	Q3ZCT0	ENTREZGENE
	U3KPS7	ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary	D3DSI0	UniProtKB/Swiss-Prot
	Q3ZCT0	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2019-01-29	LCA5L	lebercilin LCA5 like		LCA5L, lebercilin like	Symbol and/or name change	5135510	APPROVED
2016-05-31	LCA5L	LCA5L, lebercilin like		Leber congenital amaurosis 5-like	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailable


InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailable


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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