SPIDR (scaffold protein involved in DNA repair)

Gene: SPIDR (scaffold protein involved in DNA repair) Homo sapiens

Analyze

Symbol:

SPIDR

Name:

scaffold protein involved in DNA repair

RGD ID:

1603315

HGNC Page

HGNC:28971

Description:

Involved in several processes, including cellular response to camptothecin; cellular response to hydroxyurea; and regulation of double-strand break repair. Located in nuclear chromosome and nucleoplasm. Implicated in 46 XX gonadal dysgenesis.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

DNA repair-scaffolding protein; FLJ35017; hypothetical protein LOC23514; KIAA0146; ODG9; scaffolding protein involved in DNA repair; uncharacterized protein KIAA0146

RGD Orthologs

Alliance Genes

More Info

more info ...

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	8	47,260,878 - 47,736,306 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	8	47,260,878 - 47,736,306 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	8	48,173,470 - 48,648,868 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	8	48,336,095 - 48,811,028 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	8	44,177,794 - 44,633,625 (+)	NCBI		Celera
Cytogenetic Map	8	q11.21	NCBI
HuRef	8	43,638,756 - 44,111,478 (+)	NCBI		HuRef
CHM1_1	8	48,225,097 - 48,700,450 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (IAGP)

hereditary breast ovarian cancer syndrome (IAGP)

Ovarian Dysgenesis 9 (IAGP)

primary ovarian insufficiency 16 (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-schisandrin B (ISO)

17beta-hydroxy-5alpha-androstan-3-one (EXP)

2,3,7,8-tetrachlorodibenzodioxine (ISO)

4,4'-sulfonyldiphenol (EXP)

5-aza-2'-deoxycytidine (EXP)

acrolein (EXP)

aflatoxin B1 (EXP)

Aflatoxin B2 alpha (EXP)

alpha-pinene (EXP)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

arsenite(3-) (EXP)

benzo[a]pyrene (EXP)

benzo[a]pyrene diol epoxide I (EXP)

benzo[e]pyrene (EXP)

bisphenol A (EXP,ISO)

bisphenol F (EXP)

cadmium dichloride (ISO)

chlorpyrifos (ISO)

cisplatin (EXP)

cyclosporin A (EXP)

FR900359 (EXP)

fulvestrant (EXP)

methapyrilene (EXP)

nickel atom (EXP)

oxaliplatin (ISO)

ozone (EXP)

paracetamol (EXP)

sodium arsenite (EXP)

tetrachloromethane (ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

topotecan (ISO)

vitamin E (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

cellular response to camptothecin (IDA)

cellular response to hydroxyurea (IDA)

cellular response to ionizing radiation (IDA)

DNA damage response (IDA)

DNA recombination (IEA)

DNA repair (IEA)

double-strand break repair via homologous recombination (IBA,IEA,IMP)

positive regulation of double-strand break repair (IMP)

positive regulation of protein-containing complex assembly (IDA)

regulation of double-strand break repair via homologous recombination (IDA)

regulation of establishment of protein localization to chromosome (IBA,IDA,IEA)

Cellular Component

nuclear chromosome (IBA,IDA,IEA)

nucleoplasm (IBA,IDA,IEA,TAS)

nucleus (IEA)

Molecular Function

protein binding (IPI)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Abnormality of metabolism/homeostasis (IAGP)

Abnormality of secondary sexual hair (IAGP)

Ambiguous genitalia (IAGP)

Aplasia/Hypoplasia of the breasts (IAGP)

Aplasia/hypoplasia of the uterus (IAGP)

Arachnodactyly (IAGP)

Ataxia (IAGP)

Autosomal recessive inheritance (IAGP)

Decreased cirrculating antimullerian hormone circulation (IAGP)

Decreased fertility (IAGP)

Decreased serum estradiol (IAGP)

Delayed puberty (IAGP)

Delayed skeletal maturation (IAGP)

Elevated circulating follicle stimulating hormone level (IAGP)

Elevated circulating luteinizing hormone level (IAGP)

Gonadal dysgenesis (IAGP)

Hearing impairment (IAGP)

Hypoplasia of the ovary (IAGP)

Hypoplasia of the uterus (IAGP)

Increased circulating gonadotropin level (IAGP)

Juvenile onset (IAGP)

Microcephaly (IAGP)

Osteopenia (IAGP)

Osteoporosis of vertebrae (IAGP)

Premature ovarian insufficiency (IAGP)

Primary amenorrhea (IAGP)

Pulmonary fibrosis (IAGP)

Reduced bone mineral density (IAGP)

Secondary amenorrhea (IAGP)

Short stature (IAGP)

Sparse pubic hair (IAGP)

Streak ovary (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:8590280	PMID:8889548	PMID:12477932	PMID:14702039	PMID:15489334	PMID:15502879	PMID:15858003	PMID:21873635	PMID:22589738	PMID:23509288	PMID:23603433	PMID:23754376
PMID:25609649	PMID:27967308	PMID:28514442	PMID:28611215	PMID:28986522	PMID:29117863	PMID:30836988	PMID:31665741	PMID:32513696	PMID:33961781	PMID:34697795	PMID:35256949
PMID:36038948

Genomics

Comparative Map Data

SPIDR
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	8	47,260,878 - 47,736,306 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	8	48,173,470 - 48,648,868 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	8	48,336,095 - 48,811,028 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	8	44,177,794 - 44,633,625 (+)	NCBI		Celera
Cytogenetic Map	8	q11.21	NCBI
HuRef	8	43,638,756 - 44,111,478 (+)	NCBI		HuRef
CHM1_1	8	48,225,097 - 48,700,450 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI		T2T-CHM13v2.0

Spidr
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	16	15,707,088 - 15,964,715 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	16	15,707,088 - 15,964,715 (-)	Ensembl		GRCm39 Ensembl
GRCm38	16	15,889,224 - 16,146,851 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	16	15,889,224 - 16,146,851 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	16	15,889,320 - 16,146,926 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	16	15,802,805 - 16,060,411 (-)	NCBI		MGSCv36	mm8
Celera	16	16,460,508 - 16,718,485 (-)	NCBI		Celera
Cytogenetic Map	16	A2	NCBI
cM Map	16	10.09	NCBI

Spidr
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	11	98,270,779 - 98,511,760 (-)	NCBI		GRCr8
mRatBN7.2	11	84,766,593 - 85,007,597 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	11	84,766,593 - 85,007,600 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	11	93,498,564 - 93,734,667 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	11	86,159,715 - 86,395,832 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	11	85,213,308 - 85,449,420 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	11	89,009,931 - 89,260,361 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	11	89,009,931 - 89,260,297 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	11	92,071,681 - 92,113,042 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
Rnor_5.0	11	92,163,149 - 92,313,960 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	11	86,830,121 - 86,918,203 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	11	83,509,894 - 83,748,337 (-)	NCBI		Celera
Cytogenetic Map	11	q23	NCBI

Spidr
(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 Ensembl	NW_004955454	7,359,670 - 7,711,680 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955454	7,360,144 - 7,710,077 (+)	NCBI	ChiLan1.0	ChiLan1.0

SPIDR
(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	7	62,896,094 - 63,371,975 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	8	38,590,234 - 39,065,733 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	8	43,691,454 - 44,166,259 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	8	41,083,934 - 41,559,683 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	8	41,083,964 - 41,558,170 (+)	Ensembl	panpan1.1		panPan2

SPIDR
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	35	79,188 - 503,687 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	35	79,185 - 514,797 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	35	90,608 - 526,254 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	35	28,419 - 463,757 (-)	NCBI		ROS_Cfam_1.0
UMICH_Zoey_3.1	35	13,433 - 448,429 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	35	31,778 - 466,957 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	35	1,366,967 - 1,802,342 (-)	NCBI		UU_Cfam_GSD_1.0

Spidr
(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_024405303	79,731,806 - 80,126,422 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936590	4,921,542 - 5,316,195 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936590	4,921,755 - 5,041,573 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

SPIDR
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	4	79,874,831 - 80,190,655 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	4	79,874,937 - 80,190,744 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	4	87,754,732 - 87,756,996 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

SPIDR
(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	8	43,380,207 - 43,872,077 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	8	43,380,244 - 43,872,937 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666039	98,198,670 - 98,702,703 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Spidr
(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 1.0	NW_004624735	7,724,048 - 8,172,725 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in SPIDR
68 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 8p21.2-q11.21(chr8:25832130-48521849)x3	copy number gain	See cases [RCV000050904]	Chr8:25832130..48521849 [GRCh38] Chr8:25689646..49434409 [GRCh37] Chr8:25745563..49596962 [NCBI36] Chr8:8p21.2-q11.21	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3	copy number gain	See cases [RCV000051206]	Chr8:241530..145049449 [GRCh38] Chr8:191530..146274835 [GRCh37] Chr8:181530..146245639 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8p12-q11.21(chr8:29719897-48521849)x3	copy number gain	See cases [RCV000050995]	Chr8:29719897..48521849 [GRCh38] Chr8:29577413..49434409 [GRCh37] Chr8:29633332..49596962 [NCBI36] Chr8:8p12-q11.21	pathogenic
GRCh38/hg38 8p22-q11.21(chr8:14940110-47929925)x3	copy number gain	See cases [RCV000053635]	Chr8:14940110..47929925 [GRCh38] Chr8:14797619..48842485 [GRCh37] Chr8:14841990..49005038 [NCBI36] Chr8:8p22-q11.21	pathogenic
GRCh38/hg38 8p11.22-q11.21(chr8:39830633-49209461)x3	copy number gain	See cases [RCV000053649]	Chr8:39830633..49209461 [GRCh38] Chr8:39688152..50122020 [GRCh37] Chr8:39807309..50284573 [NCBI36] Chr8:8p11.22-q11.21	pathogenic
GRCh38/hg38 8p11.21-q11.21(chr8:41547961-48178799)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053651]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053651]\|See cases [RCV000053651]	Chr8:41547961..48178799 [GRCh38] Chr8:41405480..49091359 [GRCh37] Chr8:41524637..49253912 [NCBI36] Chr8:8p11.21-q11.21	pathogenic
GRCh38/hg38 8p11.21-q11.21(chr8:41845699-47893948)x3	copy number gain	See cases [RCV000053652]	Chr8:41845699..47893948 [GRCh38] Chr8:41703217..48806508 [GRCh37] Chr8:41822374..48969061 [NCBI36] Chr8:8p11.21-q11.21	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]\|See cases [RCV000053604]	Chr8:244417..145054775 [GRCh38] Chr8:194417..146280161 [GRCh37] Chr8:184417..146250965 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	copy number gain	See cases [RCV000053602]	Chr8:241530..145054634 [GRCh38] Chr8:191530..146280020 [GRCh37] Chr8:181530..146250824 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
NC_000008.11:g.47450671A>G	single nucleotide variant	Lung cancer [RCV000107413]	Chr8:47450671 [GRCh38] Chr8:48363233 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh38/hg38 8q11.1-11.21(chr8:47142202-47673614)x3	copy number gain	See cases [RCV000133794]	Chr8:47142202..47673614 [GRCh38] Chr8:48053825..48586176 [GRCh37] Chr8:48172990..48748729 [NCBI36] Chr8:8q11.1-11.21	uncertain significance
GRCh38/hg38 8q11.1-13.2(chr8:46031334-69303787)x3	copy number gain	See cases [RCV000133720]	Chr8:46031334..69303787 [GRCh38] Chr8:46942956..70216022 [GRCh37] Chr8:47062121..70378576 [NCBI36] Chr8:8q11.1-13.2	pathogenic
GRCh38/hg38 8q11.21(chr8:47276396-47303590)x3	copy number gain	See cases [RCV000134356]	Chr8:47276396..47303590 [GRCh38] Chr8:48174652..48223809 [GRCh37] Chr8:48337205..48386362 [NCBI36] Chr8:8q11.21	benign
GRCh38/hg38 8q11.21(chr8:47414028-47609983)x1	copy number loss	See cases [RCV000134343]	Chr8:47414028..47609983 [GRCh38] Chr8:48326590..48522545 [GRCh37] Chr8:48489143..48685098 [NCBI36] Chr8:8q11.21	benign\|likely benign\|conflicting data from submitters
GRCh38/hg38 8q11.1-11.21(chr8:46709224-47276395)x3	copy number gain	See cases [RCV000135715]	Chr8:46709224..47276395 [GRCh38] Chr8:47620846..48223868 [GRCh37] Chr8:47740011..48386421 [NCBI36] Chr8:8q11.1-11.21	uncertain significance
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3	copy number gain	See cases [RCV000138643]	Chr8:241605..145054781 [GRCh38] Chr8:191605..146280167 [GRCh37] Chr8:181605..146250971 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q11.1-11.21(chr8:47071019-47276395)x3	copy number gain	See cases [RCV000139171]	Chr8:47071019..47276395 [GRCh38] Chr8:47982642..48223882 [GRCh37] Chr8:48101807..48386435 [NCBI36] Chr8:8q11.1-11.21	likely benign
GRCh38/hg38 8p12-q12.1(chr8:36580103-59618998)x3	copy number gain	See cases [RCV000139582]	Chr8:36580103..59618998 [GRCh38] Chr8:36437621..60531557 [GRCh37] Chr8:36556779..60694111 [NCBI36] Chr8:8p12-q12.1	pathogenic
GRCh38/hg38 8q11.21(chr8:47701537-47918282)x3	copy number gain	See cases [RCV000140641]	Chr8:47701537..47918282 [GRCh38] Chr8:48614099..48830842 [GRCh37] Chr8:48776652..48993395 [NCBI36] Chr8:8q11.21	uncertain significance
GRCh38/hg38 8q11.21-11.23(chr8:47338394-52753188)x3	copy number gain	See cases [RCV000141920]	Chr8:47338394..52753188 [GRCh38] Chr8:48250960..53665748 [GRCh37] Chr8:48413513..53828301 [NCBI36] Chr8:8q11.21-11.23	uncertain significance
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3	copy number gain	See cases [RCV000141808]	Chr8:208048..145070385 [GRCh38] Chr8:158048..146295771 [GRCh37] Chr8:148048..146266575 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q11.1-11.21(chr8:46389911-47265481)x3	copy number gain	See cases [RCV000142305]	Chr8:46389911..47265481 [GRCh38] Chr8:47301533..48178073 [GRCh37] Chr8:47420698..48340626 [NCBI36] Chr8:8q11.1-11.21	uncertain significance
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3	copy number gain	See cases [RCV000142021]	Chr8:21291522..145070385 [GRCh38] Chr8:21149033..146295771 [GRCh37] Chr8:21193313..146266575 [NCBI36] Chr8:8p21.3-q24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3	copy number gain	See cases [RCV000142858]	Chr8:226452..145068712 [GRCh38] Chr8:176452..146294098 [GRCh37] Chr8:166452..146264902 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	copy number gain	See cases [RCV000148092]	Chr8:241530..145054634 [GRCh38] Chr8:191530..146280020 [GRCh37] Chr8:181530..146250824 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3	copy number gain	not provided [RCV000848192]	Chr8:31936551..146295771 [GRCh37] Chr8:8p12-q24.3	pathogenic
GRCh37/hg19 8q11.21(chr8:48587984-48780185)x1	copy number loss	See cases [RCV000449313]	Chr8:48587984..48780185 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8q11.1-11.21(chr8:46912309-50818801)x3	copy number gain	See cases [RCV000447547]	Chr8:46912309..50818801 [GRCh37] Chr8:8q11.1-11.21	uncertain significance
GRCh37/hg19 8p21.2-q12.1(chr8:24772064-24813176)x3	copy number gain	See cases [RCV000446588]	Chr8:24772064..24813176 [GRCh37] Chr8:8p21.2-q12.1	uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3	copy number gain	See cases [RCV000447507]	Chr8:158991..146280828 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)	copy number gain	See cases [RCV000510234]	Chr8:158049..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q11.1-11.21(chr8:47301533-48178073)x4	copy number gain	See cases [RCV000510422]	Chr8:47301533..48178073 [GRCh37] Chr8:8q11.1-11.21	uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3	copy number gain	See cases [RCV000511095]	Chr8:158049..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
NM_001080394.4(SPIDR):c.1238C>T (p.Ser413Phe)	single nucleotide variant	Inborn genetic diseases [RCV003297994]	Chr8:47595951 [GRCh38] Chr8:48508513 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1592A>T (p.His531Leu)	single nucleotide variant	Inborn genetic diseases [RCV003307083]	Chr8:47673848 [GRCh38] Chr8:48586410 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.305G>T (p.Ser102Ile)	single nucleotide variant	Inborn genetic diseases [RCV003281148]	Chr8:47291081 [GRCh38] Chr8:48203670 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3	copy number gain	See cases [RCV000512169]	Chr8:12490999..146295771 [GRCh37] Chr8:8p23.1-q24.3	pathogenic
GRCh37/hg19 8q11.1-11.21(chr8:47294183-48179333)x4	copy number gain	See cases [RCV000663386]	Chr8:47294183..48179333 [GRCh37] Chr8:8q11.1-11.21	uncertain significance
GRCh37/hg19 8q11.1-11.23(chr8:46863521-55218838)x3	copy number gain	not provided [RCV000683033]	Chr8:46863521..55218838 [GRCh37] Chr8:8q11.1-11.23	uncertain significance
GRCh37/hg19 8q11.21(chr8:48609394-48892709)x3	copy number gain	not provided [RCV000682964]	Chr8:48609394..48892709 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8q11.1-11.21(chr8:47301533-48178073)x4	copy number gain	not provided [RCV000683002]	Chr8:47301533..48178073 [GRCh37] Chr8:8q11.1-11.21	uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3	copy number gain	not provided [RCV000747254]	Chr8:164984..146293414 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3	copy number gain	not provided [RCV000747248]	Chr8:10213..146293414 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
NM_001080394.4(SPIDR):c.1078G>C (p.Val360Leu)	single nucleotide variant	not provided [RCV000918487]	Chr8:47440523 [GRCh38] Chr8:48353085 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.884A>C (p.Lys295Thr)	single nucleotide variant	not provided [RCV000902867]	Chr8:47440329 [GRCh38] Chr8:48352891 [GRCh37] Chr8:8q11.21	likely benign\|conflicting interpretations of pathogenicity
NM_001080394.4(SPIDR):c.2426C>T (p.Pro809Leu)	single nucleotide variant	not provided [RCV000900727]	Chr8:47727284 [GRCh38] Chr8:48639846 [GRCh37] Chr8:8q11.21	benign
NM_001080394.4(SPIDR):c.947T>A (p.Met316Lys)	single nucleotide variant	not provided [RCV000971142]	Chr8:47440392 [GRCh38] Chr8:48352954 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.2270A>G (p.Glu757Gly)	single nucleotide variant	not provided [RCV000924115]	Chr8:47713570 [GRCh38] Chr8:48626132 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.877+6G>A	single nucleotide variant	not provided [RCV000948340]	Chr8:47407967 [GRCh38] Chr8:48320529 [GRCh37] Chr8:8q11.21	benign
NM_001080394.4(SPIDR):c.1954A>G (p.Thr652Ala)	single nucleotide variant	not provided [RCV000968128]	Chr8:47701992 [GRCh38] Chr8:48614554 [GRCh37] Chr8:8q11.21	benign
NM_001080394.4(SPIDR):c.1773+9G>A	single nucleotide variant	not provided [RCV000963062]	Chr8:47700499 [GRCh38] Chr8:48613061 [GRCh37] Chr8:8q11.21	benign
NM_001080394.4(SPIDR):c.1978-8A>C	single nucleotide variant	not provided [RCV000895911]	Chr8:47712654 [GRCh38] Chr8:48625216 [GRCh37] Chr8:8q11.21	benign
NM_001080394.4(SPIDR):c.639A>G (p.Ala213=)	single nucleotide variant	not provided [RCV000916459]	Chr8:47396489 [GRCh38] Chr8:48309049 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.1977+25_1977+32del	microsatellite	not provided [RCV000899685]	Chr8:47702025..47702032 [GRCh38] Chr8:48614587..48614594 [GRCh37] Chr8:8q11.21	likely benign
NC_000008.10:g.(?_48270390)_(49987806_?)del	deletion	not provided [RCV000819887]	Chr8:48270390..49987806 [GRCh37] Chr8:8q11.21	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	copy number gain	not provided [RCV000848478]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q11.1-11.21(chr8:47301533-48178073)x4	copy number gain	not provided [RCV000849672]	Chr8:47301533..48178073 [GRCh37] Chr8:8q11.1-11.21	uncertain significance
GRCh37/hg19 8q11.1-11.21(chr8:46851293-48277752)x3	copy number gain	not provided [RCV000847953]	Chr8:46851293..48277752 [GRCh37] Chr8:8q11.1-11.21	uncertain significance
GRCh37/hg19 8q11.21(chr8:48293202-48551216)x1	copy number loss	not provided [RCV000849668]	Chr8:48293202..48551216 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8q11.21(chr8:48128306-48205935)x1	copy number loss	not provided [RCV000848912]	Chr8:48128306..48205935 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8p11.22-q12.3(chr8:39555657-64049089)x3	copy number gain	not provided [RCV000846266]	Chr8:39555657..64049089 [GRCh37] Chr8:8p11.22-q12.3	pathogenic
NM_001080394.4(SPIDR):c.1083G>C (p.Arg361=)	single nucleotide variant	not provided [RCV000885987]	Chr8:47440528 [GRCh38] Chr8:48353090 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.212C>T (p.Thr71Met)	single nucleotide variant	Inborn genetic diseases [RCV003242615]	Chr8:47284050 [GRCh38] Chr8:48196639 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1648G>C (p.Val550Leu)	single nucleotide variant	not provided [RCV001532141]	Chr8:47673904 [GRCh38] Chr8:48586466 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.776+1G>T	single nucleotide variant	Genetic non-acquired premature ovarian failure [RCV001661758]	Chr8:47396627 [GRCh38] Chr8:48309187 [GRCh37] Chr8:8q11.21	pathogenic
NM_001080394.4(SPIDR):c.2265del (p.Cys756fs)	deletion	Genetic non-acquired premature ovarian failure [RCV001661759]	Chr8:47713564 [GRCh38] Chr8:48626126 [GRCh37] Chr8:8q11.21	pathogenic
NM_001080394.4(SPIDR):c.2192G>A (p.Arg731Gln)	single nucleotide variant	not provided [RCV001532142]	Chr8:47713492 [GRCh38] Chr8:48626054 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8q11.1-11.21(chr8:48058961-48260865)x1	copy number loss	not provided [RCV001006102]	Chr8:48058961..48260865 [GRCh37] Chr8:8q11.1-11.21	uncertain significance
GRCh37/hg19 8q11.1-11.21(chr8:48089553-48222687)x1	copy number loss	not provided [RCV001258405]	Chr8:48089553..48222687 [GRCh37] Chr8:8q11.1-11.21	uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)	copy number gain	Polydactyly [RCV002280629]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
NM_001080394.4(SPIDR):c.839G>A (p.Trp280Ter)	single nucleotide variant	Ovarian dysgenesis 9 [RCV001795888]	Chr8:47407923 [GRCh38] Chr8:48320485 [GRCh37] Chr8:8q11.21	pathogenic
NM_001080394.4(SPIDR):c.814C>T (p.Arg272Ter)	single nucleotide variant	Ovarian dysgenesis 9 [RCV001795889]	Chr8:47407898 [GRCh38] Chr8:48320460 [GRCh37] Chr8:8q11.21	pathogenic
GRCh37/hg19 8q11.21(chr8:48336764-48752512)x1	copy number loss	not provided [RCV001829259]	Chr8:48336764..48752512 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8q11.21(chr8:48587984-48780185)	copy number loss	not specified [RCV002053762]	Chr8:48587984..48780185 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8p11.21-q11.21(chr8:42162574-48757095)	copy number gain	not specified [RCV002053760]	Chr8:42162574..48757095 [GRCh37] Chr8:8p11.21-q11.21	uncertain significance
GRCh37/hg19 8q11.1-11.21(chr8:46912309-50818801)	copy number gain	not specified [RCV002053761]	Chr8:46912309..50818801 [GRCh37] Chr8:8q11.1-11.21	uncertain significance
NM_001080394.4(SPIDR):c.295A>G (p.Ile99Val)	single nucleotide variant	Inborn genetic diseases [RCV003283790]	Chr8:47291071 [GRCh38] Chr8:48203660 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2130G>T (p.Glu710Asp)	single nucleotide variant	Inborn genetic diseases [RCV002969357]	Chr8:47712814 [GRCh38] Chr8:48625376 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.121G>T (p.Ala41Ser)	single nucleotide variant	Inborn genetic diseases [RCV002751679]	Chr8:47279949 [GRCh38] Chr8:48192537 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.334G>C (p.Asp112His)	single nucleotide variant	Inborn genetic diseases [RCV002687308]	Chr8:47291110 [GRCh38] Chr8:48203699 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1361G>A (p.Arg454His)	single nucleotide variant	Inborn genetic diseases [RCV002817914]	Chr8:47599013 [GRCh38] Chr8:48511575 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.1180T>C (p.Ser394Pro)	single nucleotide variant	Inborn genetic diseases [RCV002773260]	Chr8:47595893 [GRCh38] Chr8:48508455 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.7C>A (p.Arg3Ser)	single nucleotide variant	Inborn genetic diseases [RCV002973269]	Chr8:47260965 [GRCh38] Chr8:48173557 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1696A>T (p.Ile566Phe)	single nucleotide variant	Inborn genetic diseases [RCV002865377]	Chr8:47700413 [GRCh38] Chr8:48612975 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2098C>T (p.Pro700Ser)	single nucleotide variant	Inborn genetic diseases [RCV002864770]	Chr8:47712782 [GRCh38] Chr8:48625344 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.14G>A (p.Ser5Asn)	single nucleotide variant	Inborn genetic diseases [RCV002882830]	Chr8:47260972 [GRCh38] Chr8:48173564 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2029G>A (p.Asp677Asn)	single nucleotide variant	Inborn genetic diseases [RCV002844387]	Chr8:47712713 [GRCh38] Chr8:48625275 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.220G>C (p.Glu74Gln)	single nucleotide variant	Inborn genetic diseases [RCV002762134]	Chr8:47284058 [GRCh38] Chr8:48196647 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1986T>A (p.Ser662Arg)	single nucleotide variant	Inborn genetic diseases [RCV002693297]	Chr8:47712670 [GRCh38] Chr8:48625232 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.890G>A (p.Gly297Asp)	single nucleotide variant	Inborn genetic diseases [RCV002692386]	Chr8:47440335 [GRCh38] Chr8:48352897 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.439G>A (p.Glu147Lys)	single nucleotide variant	Inborn genetic diseases [RCV002799275]	Chr8:47293944 [GRCh38] Chr8:48206533 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.992G>A (p.Ser331Asn)	single nucleotide variant	Inborn genetic diseases [RCV002707171]	Chr8:47440437 [GRCh38] Chr8:48352999 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.35G>A (p.Arg12Lys)	single nucleotide variant	Inborn genetic diseases [RCV002980746]	Chr8:47279863 [GRCh38] Chr8:48192451 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2200T>G (p.Cys734Gly)	single nucleotide variant	Inborn genetic diseases [RCV002798725]	Chr8:47713500 [GRCh38] Chr8:48626062 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1550G>C (p.Cys517Ser)	single nucleotide variant	Inborn genetic diseases [RCV002931243]	Chr8:47673806 [GRCh38] Chr8:48586368 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1391C>A (p.Ser464Tyr)	single nucleotide variant	Inborn genetic diseases [RCV002696951]	Chr8:47599043 [GRCh38] Chr8:48511605 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1405G>T (p.Val469Leu)	single nucleotide variant	Inborn genetic diseases [RCV002744286]	Chr8:47599057 [GRCh38] Chr8:48511619 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2633A>G (p.Lys878Arg)	single nucleotide variant	Inborn genetic diseases [RCV002698990]	Chr8:47735335 [GRCh38] Chr8:48647897 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.202G>A (p.Glu68Lys)	single nucleotide variant	Inborn genetic diseases [RCV002804726]	Chr8:47284040 [GRCh38] Chr8:48196629 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2542A>G (p.Lys848Glu)	single nucleotide variant	Inborn genetic diseases [RCV002673724]	Chr8:47729039 [GRCh38] Chr8:48641601 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1933A>C (p.Thr645Pro)	single nucleotide variant	Inborn genetic diseases [RCV002835468]	Chr8:47701971 [GRCh38] Chr8:48614533 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2428G>A (p.Glu810Lys)	single nucleotide variant	Inborn genetic diseases [RCV002934598]	Chr8:47727286 [GRCh38] Chr8:48639848 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1639T>C (p.Cys547Arg)	single nucleotide variant	Inborn genetic diseases [RCV002934446]	Chr8:47673895 [GRCh38] Chr8:48586457 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1388A>T (p.Asp463Val)	single nucleotide variant	Inborn genetic diseases [RCV002675337]	Chr8:47599040 [GRCh38] Chr8:48511602 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.563G>A (p.Ser188Asn)	single nucleotide variant	Inborn genetic diseases [RCV002960439]	Chr8:47396413 [GRCh38] Chr8:48308973 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1108A>G (p.Ile370Val)	single nucleotide variant	Inborn genetic diseases [RCV002919906]	Chr8:47595821 [GRCh38] Chr8:48508383 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1754G>A (p.Arg585His)	single nucleotide variant	Inborn genetic diseases [RCV002655370]	Chr8:47700471 [GRCh38] Chr8:48613033 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.131C>T (p.Ser44Phe)	single nucleotide variant	Inborn genetic diseases [RCV003190222]	Chr8:47279959 [GRCh38] Chr8:48192547 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2321A>T (p.Asn774Ile)	single nucleotide variant	Inborn genetic diseases [RCV003211931]	Chr8:47713621 [GRCh38] Chr8:48626183 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1855G>A (p.Glu619Lys)	single nucleotide variant	Inborn genetic diseases [RCV003197115]	Chr8:47701802 [GRCh38] Chr8:48614364 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2293G>A (p.Asp765Asn)	single nucleotide variant	Inborn genetic diseases [RCV003196820]	Chr8:47713593 [GRCh38] Chr8:48626155 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.97A>G (p.Arg33Gly)	single nucleotide variant	Inborn genetic diseases [RCV003310265]	Chr8:47279925 [GRCh38] Chr8:48192513 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8p11.23-q11.21(chr8:36763176-50929707)x3	copy number gain	See cases [RCV003329560]	Chr8:36763176..50929707 [GRCh37] Chr8:8p11.23-q11.21	pathogenic
NM_001080394.4(SPIDR):c.1258A>G (p.Ile420Val)	single nucleotide variant	Inborn genetic diseases [RCV003375079]	Chr8:47595971 [GRCh38] Chr8:48508533 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1610C>T (p.Ser537Leu)	single nucleotide variant	Inborn genetic diseases [RCV003370610]	Chr8:47673866 [GRCh38] Chr8:48586428 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.1894C>T (p.Arg632Cys)	single nucleotide variant	Inborn genetic diseases [RCV003368856]	Chr8:47701841 [GRCh38] Chr8:48614403 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8p11.1-q11.21(chr8:43312712-48892709)x3	copy number gain	not provided [RCV003484733]	Chr8:43312712..48892709 [GRCh37] Chr8:8p11.1-q11.21	uncertain significance
GRCh37/hg19 8q11.21(chr8:48570047-48787917)x3	copy number gain	not provided [RCV003484734]	Chr8:48570047..48787917 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh37/hg19 8q11.21(chr8:48646558-49004354)x3	copy number gain	not provided [RCV003484735]	Chr8:48646558..49004354 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2653del (p.Cys885fs)	deletion	Ovarian dysgenesis 9 [RCV003444432]	Chr8:47735354 [GRCh38] Chr8:48647916 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.2410A>C (p.Arg804=)	single nucleotide variant	not provided [RCV003423921]	Chr8:47727268 [GRCh38] Chr8:48639830 [GRCh37] Chr8:8q11.21	likely benign
GRCh37/hg19 8p21.2-q21.3(chr8:27024288-89410121)x3	copy number gain	not specified [RCV003986754]	Chr8:27024288..89410121 [GRCh37] Chr8:8p21.2-q21.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	copy number gain	not specified [RCV003986742]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
NM_001080394.4(SPIDR):c.256+7A>G	single nucleotide variant	not provided [RCV003887193]	Chr8:47284101 [GRCh38] Chr8:48196690 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.526-8T>C	single nucleotide variant	not provided [RCV003887194]	Chr8:47396368 [GRCh38] Chr8:48308928 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.526-1387G>A	single nucleotide variant	SPIDR-related condition [RCV003968992]	Chr8:47394989 [GRCh38] Chr8:48307549 [GRCh37] Chr8:8q11.21	likely benign
NM_001080394.4(SPIDR):c.1085T>A (p.Ile362Asn)	single nucleotide variant	Inborn genetic diseases [RCV003352551]	Chr8:47440530 [GRCh38] Chr8:48353092 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.3:c.1544+13812A>T	single nucleotide variant	Lung cancer [RCV000107414]	Chr8:47613008 [GRCh38] Chr8:48525570 [GRCh37] Chr8:8q11.21	uncertain significance
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3	copy number gain	See cases [RCV000139539]	Chr8:46031340..139285494 [GRCh38] Chr8:46942962..140297737 [GRCh37] Chr8:47062127..140366919 [NCBI36] Chr8:8q11.1-24.3	pathogenic
GRCh37/hg19 8q11.21(chr8:48128092-48218014)x1	copy number loss	not provided [RCV000682923]	Chr8:48128092..48218014 [GRCh37] Chr8:8q11.21	uncertain significance
NM_001080394.4(SPIDR):c.1978-10C>T	single nucleotide variant	not provided [RCV000907019]	Chr8:47712652 [GRCh38] Chr8:48625214 [GRCh37] Chr8:8q11.21	benign
NM_001080394.4(SPIDR):c.1448G>A (p.Arg483Gln)	single nucleotide variant	Inborn genetic diseases [RCV002722454]	Chr8:47599100 [GRCh38] Chr8:48511662 [GRCh37] Chr8:8q11.21	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	7176
Count of miRNA genes:	1316
Interacting mature miRNAs:	1717
Transcripts:	ENST00000297423, ENST00000517619, ENST00000517693, ENST00000517824, ENST00000518060, ENST00000518074, ENST00000518692, ENST00000518711, ENST00000519141, ENST00000519362, ENST00000519401, ENST00000519661, ENST00000521214, ENST00000521550, ENST00000521798, ENST00000521918, ENST00000522117, ENST00000522222, ENST00000522321, ENST00000522900, ENST00000523814, ENST00000524006, ENST00000524033, ENST00000524126, ENST00000524141, ENST00000524157, ENST00000541342, ENST00000588781
Prediction methods:	Microtar, Miranda, Rnahybrid
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.

Markers in Region

A009N15

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,589,688 - 48,589,840	UniSTS	GRCh37
Build 36	8	48,752,241 - 48,752,393	RGD	NCBI36
Celera	8	44,574,849 - 44,575,001	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,052,618 - 44,052,770	UniSTS
GeneMap99-GB4 RH Map	8	246.72	UniSTS
NCBI RH Map	8	666.6	UniSTS

RH78174

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,648,649 - 48,648,798	UniSTS	GRCh37
Build 36	8	48,811,202 - 48,811,351	RGD	NCBI36
Celera	8	44,633,799 - 44,633,948	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,111,564 - 44,111,713	UniSTS
GeneMap99-GB4 RH Map	8	252.14	UniSTS
NCBI RH Map	8	675.4	UniSTS

RH79727

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,647,073 - 48,647,314	UniSTS	GRCh37
Build 36	8	48,809,626 - 48,809,867	RGD	NCBI36
Celera	8	44,632,223 - 44,632,464	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,109,988 - 44,110,229	UniSTS
GeneMap99-GB4 RH Map	8	275.67	UniSTS

RH80523

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	1,424,204 - 1,424,444	UniSTS	GRCh37
GRCh37	8	48,423,405 - 48,423,644	UniSTS	GRCh37
Build 36	8	48,585,958 - 48,586,197	RGD	NCBI36
Celera	8	44,408,616 - 44,408,855	RGD
Celera	20	1,520,555 - 1,520,795	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	43,886,933 - 43,887,172	UniSTS
HuRef	20	1,375,085 - 1,375,325	UniSTS
GeneMap99-GB4 RH Map	20	10.83	UniSTS

RH40570

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,493,774 - 48,493,967	UniSTS	GRCh37
Build 36	8	48,656,327 - 48,656,520	RGD	NCBI36
Celera	8	44,478,961 - 44,479,154	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	43,956,756 - 43,956,949	UniSTS

RH68757

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,265,846 - 48,265,969	UniSTS	GRCh37
Build 36	8	48,428,399 - 48,428,522	RGD	NCBI36
Celera	8	44,251,078 - 44,251,201	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	43,731,013 - 43,731,136	UniSTS

G43519

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,648,662 - 48,648,811	UniSTS	GRCh37
Build 36	8	48,811,215 - 48,811,364	RGD	NCBI36
Celera	8	44,633,812 - 44,633,961	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,111,577 - 44,111,726	UniSTS

RH102674

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,493,146 - 48,493,280	UniSTS	GRCh37
Build 36	8	48,655,699 - 48,655,833	RGD	NCBI36
Celera	8	44,478,333 - 44,478,467	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	43,956,128 - 43,956,262	UniSTS

SHGC-85736

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,511,221 - 48,511,504	UniSTS	GRCh37
Build 36	8	48,673,774 - 48,674,057	RGD	NCBI36
Celera	8	44,496,406 - 44,496,689	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	43,974,205 - 43,974,488	UniSTS
TNG Radiation Hybrid Map	8	24176.0	UniSTS

G59783

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,648,676 - 48,648,791	UniSTS	GRCh37
Build 36	8	48,811,229 - 48,811,344	RGD	NCBI36
Celera	8	44,633,826 - 44,633,941	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,111,591 - 44,111,706	UniSTS
TNG Radiation Hybrid Map	8	24114.0	UniSTS

D8S359

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,647,613 - 48,647,742	UniSTS	GRCh37
Build 36	8	48,810,166 - 48,810,295	RGD	NCBI36
Celera	8	44,632,763 - 44,632,892	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,110,528 - 44,110,657	UniSTS

SHGC-112129

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	21,867 - 22,172	UniSTS	GRCh37
GRCh37	8	48,197,339 - 48,197,644	UniSTS	GRCh37
Build 36	8	48,359,892 - 48,360,197	RGD	NCBI36
Celera	8	44,182,572 - 44,182,877	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	43,662,509 - 43,662,814	UniSTS
TNG Radiation Hybrid Map	8	24279.0	UniSTS

SHGC-105289

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,392,687 - 48,392,996	UniSTS	GRCh37
Build 36	8	48,555,240 - 48,555,549	RGD	NCBI36
Celera	8	44,377,898 - 44,378,207	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	43,856,225 - 43,856,534	UniSTS
TNG Radiation Hybrid Map	8	24206.0	UniSTS

SHGC-149722

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,573,757 - 48,574,097	UniSTS	GRCh37
Build 36	8	48,736,310 - 48,736,650	RGD	NCBI36
Celera	8	44,558,917 - 44,559,257	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,036,691 - 44,037,031	UniSTS
TNG Radiation Hybrid Map	8	24146.0	UniSTS

G19638

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,648,259 - 48,648,453	UniSTS	GRCh37
Build 36	8	48,810,812 - 48,811,006	RGD	NCBI36
Celera	8	44,633,409 - 44,633,603	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,111,174 - 44,111,368	UniSTS

A001T40

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,648,259 - 48,648,453	UniSTS	GRCh37
Build 36	8	48,810,812 - 48,811,006	RGD	NCBI36
Celera	8	44,633,409 - 44,633,603	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,111,174 - 44,111,368	UniSTS
GeneMap99-GB4 RH Map	8	249.52	UniSTS
NCBI RH Map	8	671.5	UniSTS

G32171

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,591,114 - 48,591,345	UniSTS	GRCh37
Build 36	8	48,753,667 - 48,753,898	RGD	NCBI36
Celera	8	44,576,275 - 44,576,506	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,054,044 - 44,054,275	UniSTS

AFMB290WB9

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,614,543 - 48,614,820	UniSTS	GRCh37
Build 36	8	48,777,096 - 48,777,373	RGD	NCBI36
Celera	8	44,599,704 - 44,599,963	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,077,472 - 44,077,731	UniSTS

RH36389

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,493,724 - 48,493,824	UniSTS	GRCh37
Build 36	8	48,656,277 - 48,656,377	RGD	NCBI36
Celera	8	44,478,911 - 44,479,011	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	43,956,706 - 43,956,806	UniSTS
GeneMap99-GB4 RH Map	8	246.93	UniSTS
NCBI RH Map	8	664.1	UniSTS

RH77701

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,648,389 - 48,648,490	UniSTS	GRCh37
Build 36	8	48,810,942 - 48,811,043	RGD	NCBI36
Celera	8	44,633,539 - 44,633,640	RGD
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,111,304 - 44,111,405	UniSTS
GeneMap99-GB4 RH Map	8	267.83	UniSTS
NCBI RH Map	8	679.5	UniSTS

G32681

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	48,589,688 - 48,589,840	UniSTS	GRCh37
Celera	8	44,574,849 - 44,575,001	UniSTS
Cytogenetic Map	8	q11.21	UniSTS
HuRef	8	44,052,618 - 44,052,770	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

2255

1749

1399

317

1389

166

3670

1090

2387

271

1383

1603

166

1200

2142

Low

184

1242

327

307

562

299

687

1107

1347

148

646

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001080394	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001282916	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001282919	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352931	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352932	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352933	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352934	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352935	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352936	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352937	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352938	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352939	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352940	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352941	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352942	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352943	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352944	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352945	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352946	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352947	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352948	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352949	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352950	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352951	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352952	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352953	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352955	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352956	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352957	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352958	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352959	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352960	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352961	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_104581	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_148202	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_148203	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_148204	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_148205	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011517497	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013268	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013269	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013270	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013271	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013273	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013274	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013279	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013280	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013281	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017013289	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024447116	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024447117	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421638	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421639	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421640	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421641	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421642	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421643	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421644	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421645	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421646	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421647	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421648	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421649	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421650	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421651	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421652	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360202	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360203	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360204	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360205	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360206	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360207	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360208	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360209	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360210	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360211	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360212	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360213	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360214	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360215	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360216	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360217	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360218	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360219	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360220	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360221	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360222	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054360223	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001745508	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC023991	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC024451	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC024649	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC104995	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC142471	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC145060	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC225614	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC231773	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC233269	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK026929	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK055680	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK092336	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK095778	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK122820	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK293809	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK293972	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK294248	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK294275	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK297681	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK301677	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK303140	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK303579	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK309842	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK310584	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC015561	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC031627	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM981420	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068270	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	D63480	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DR000775	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY012281	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF458749	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OP794608	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000297423 ⟹ ENSP00000297423

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,938 - 47,736,306 (+)	Ensembl

RefSeq Acc Id:

ENST00000517619 ⟹ ENSP00000427878

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,727,196 - 47,735,374 (+)	Ensembl

RefSeq Acc Id:

ENST00000517693 ⟹ ENSP00000427889

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,659,664 - 47,735,911 (+)	Ensembl

RefSeq Acc Id:

ENST00000517824 ⟹ ENSP00000430965

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,942 - 47,440,542 (+)	Ensembl

RefSeq Acc Id:

ENST00000518060 ⟹ ENSP00000429448

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,727,253 - 47,735,513 (+)	Ensembl

RefSeq Acc Id:

ENST00000518074 ⟹ ENSP00000429487

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,931 - 47,735,529 (+)	Ensembl

RefSeq Acc Id:

ENST00000518692

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,697,756 - 47,713,533 (+)	Ensembl

RefSeq Acc Id:

ENST00000518711

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,728,720 - 47,729,704 (+)	Ensembl

RefSeq Acc Id:

ENST00000519141

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,654,088 - 47,735,883 (+)	Ensembl

RefSeq Acc Id:

ENST00000519362

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,673,533 - 47,735,785 (+)	Ensembl

RefSeq Acc Id:

ENST00000519401 ⟹ ENSP00000429193

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,440,401 - 47,735,916 (+)	Ensembl

RefSeq Acc Id:

ENST00000519661 ⟹ ENSP00000428287

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,955 - 47,599,035 (+)	Ensembl

RefSeq Acc Id:

ENST00000521214

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,276,833 - 47,735,911 (+)	Ensembl

RefSeq Acc Id:

ENST00000521550

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,942 - 47,713,091 (+)	Ensembl

RefSeq Acc Id:

ENST00000521798

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,291,053 - 47,294,428 (+)	Ensembl

RefSeq Acc Id:

ENST00000521918

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,360,819 - 47,440,397 (+)	Ensembl

RefSeq Acc Id:

ENST00000522117 ⟹ ENSP00000429805

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,956 - 47,735,511 (+)	Ensembl

RefSeq Acc Id:

ENST00000522222 ⟹ ENSP00000430664

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,955 - 47,388,444 (+)	Ensembl

RefSeq Acc Id:

ENST00000522321

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,688,442 - 47,713,644 (+)	Ensembl

RefSeq Acc Id:

ENST00000522900

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,936 - 47,388,484 (+)	Ensembl

RefSeq Acc Id:

ENST00000523814 ⟹ ENSP00000428222

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,913 - 47,408,006 (+)	Ensembl

RefSeq Acc Id:

ENST00000524006 ⟹ ENSP00000430091

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,965 - 47,599,043 (+)	Ensembl

RefSeq Acc Id:

ENST00000524033 ⟹ ENSP00000429997

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,956 - 47,595,984 (+)	Ensembl

RefSeq Acc Id:

ENST00000524126 ⟹ ENSP00000430941

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,953 - 47,735,913 (+)	Ensembl

RefSeq Acc Id:

ENST00000524141

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,955 - 47,713,441 (+)	Ensembl

RefSeq Acc Id:

ENST00000524157

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,407,861 - 47,419,268 (+)	Ensembl

RefSeq Acc Id:

ENST00000541342 ⟹ ENSP00000444061

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,260,878 - 47,735,999 (+)	Ensembl

RefSeq Acc Id:

ENST00000588781

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	47,732,559 - 47,735,327 (+)	Ensembl

RefSeq Acc Id:

NM_001080394 ⟹ NP_001073863

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,938 - 47,736,306 (+)	NCBI
GRCh37	8	48,173,489 - 48,648,563 (+)	ENTREZGENE
Build 36	8	48,336,095 - 48,811,028 (+)	NCBI Archive
Celera	8	44,177,794 - 44,633,625 (+)	RGD
HuRef	8	43,638,756 - 44,111,478 (+)	NCBI
CHM1_1	8	48,225,078 - 48,700,450 (+)	NCBI
T2T-CHM13v2.0	8	47,636,700 - 48,112,023 (+)	NCBI

Sequence:

show sequence

GCTCAGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGA
GTTGGAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCT
CAGGACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAG
AACACTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAAT
TATGCCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAAC
ATGGAGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGAT
GAATTACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAAT
TTGAAGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTT
GACAAGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCA
TCAGATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACA
AATACCACGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGAC
AAAATCAACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCA
GAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGA
ATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTC
AGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAA
GTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCA
GGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCC
CCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCT
GTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTG
AAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAAT
TAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGG
ACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGG
ATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGT
GGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGC
TCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGT
TCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAG
CCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTG
ATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAG
AGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGG
ACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGC
TTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTT
ACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGAC
CGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTAT
GTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACA
GCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCT
CTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCG
GTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTG
TGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAG
ATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACA
TCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAG
TGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGG
GAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCC
GTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGG
CCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGG
TGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGA
TCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATC
AAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTT
TCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTT
TTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTAC
AGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATAT
TACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATG
TTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAACTGGTGTG
ATCGTGTCTCTGCTGAATGGTGGTGGGGATAGCTGGCTCCACCACACACACCTGTTTTAATTAG
GCTGGGTAATGTGCACGGAGAGCAAAGATCACAGACTAAGGAGCAGTCAGTCGGATATTTGCTT
TGCTGGCAAAGATTTAAACCAAGAATTAATTATCTTTGGACACTATAAAGATTTTGTTCCCTTC
CTTATAGCAATATAATCATGACAGGCCATGGTTAACTACATCAGATACACGTAGCAGCCGTGAC
CAAGACATGGTGCCCTAATACCAAGTGTTCTTGGGTTAAAG

hide sequence

RefSeq Acc Id:

NM_001282916 ⟹ NP_001269845

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
HuRef	8	43,638,756 - 44,111,478 (+)	NCBI
CHM1_1	8	48,225,078 - 48,700,450 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGC
TCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAATTAC
AGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGAAGA
TGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACAAGT
GATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATA
GTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCA
CGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCA
ACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATT
CAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGA
GAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGA
AAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCA
TGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGG
AGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGAC
ACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTC
TGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTA
CTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGT
CTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCT
GGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCT
CCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTG
CAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGAC
ACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGA
AGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTG
GGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACA
CCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAA
AACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATT
GATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAG
ACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAA
ACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTC
ACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCC
CCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTT
CTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTT
CAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGC
TCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGG
CGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAA
CAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTG
TTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGT
CAAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTAC
GAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCG
CCCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGC
AGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGT
GGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAA
ATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATAC
CTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATT
GAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGT
TCATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTT
AACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTT
CTGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGG
GAACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAAAAAAAAAAAAAAAAA
A

hide sequence

RefSeq Acc Id:

NM_001282919 ⟹ NP_001269848

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
HuRef	8	43,638,756 - 44,111,478 (+)	NCBI
CHM1_1	8	48,225,078 - 48,700,450 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGTCATTAACAGCTGAAGAGAAGAC
GATTACAGAAAAGCACCTTGAATTATGCCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGC
ACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGA
CACTTTCTCAGTTACAGAGAGATGAATTACAGTTTATCGACTGGGAGATTGACAGTGACAGGGC
AGAGGCTAGTGACTGTGATGAATTTGAAGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCT
TCTTGTGCAAGTAATCAGTCTTTGACAAGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTT
CTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACT
CATTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGGATGCAAGACAGATTATG
GAGAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCATACACCTCAGAAACCCA
CAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGC
AGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGT
ATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGC
TGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAG
CTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACT
GCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGA
TTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAA
AGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATC
TCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGT
GTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCAT
CCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCG
TGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCA
CCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCT
GGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGA
CAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAA
GGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACC
TGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATC
CTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTT
ACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTG
CAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAA
AGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGC
TCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGC
ACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATT
GTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAA
GTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTC
CATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTG
TGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTG
GGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTG
CCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGGTAGGAGCCAGGCCAGAGCACGCACGCACT
CCTAGCTCACTCCAACATAGCGAAGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGG
TTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAA
TCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAAC
TTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTAT
GGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAG
ATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAA
ATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTT
AGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTAC
CATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTA
AACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTG
CAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAA
AGTGTAGCTCTCTGAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_001352931 ⟹ NP_001339860

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAG
ATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATA
CCACGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAA
TCAACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAA
ATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCG
AGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGT
AGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTG
CCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCC
TGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAG
GACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTA
TTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGT
GTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAG
GGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAG
CCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTC
TCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTG
GTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAG
GACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGG
TGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTG
GTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTG
ACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGAT
AAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAA
ATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAA
GAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCA
AAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGAT
GTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGG
CCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCT
CTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTG
CTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGA
TGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGT
TGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTG
GAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTC
CTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAA
GGTCAAGGTAGGAGCCAGGCCAGAGCACGCACGCACTCCTAGCTCACTCCAACATAGCGAAGCT
GTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTG
AAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACC
CGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACA
CTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGT
GATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAA
CTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTT
CTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCT
TAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTT
GTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATT
CCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTA
CAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTG
TATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352932 ⟹ NP_001339861

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGTGTGCC
TGATAGAAGGTGACTACCCAAGCAGTTTTTTTGACGAGCCAAGTTCTATAGAAATTTTAGAGTA
TTCATCAGATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCT
CACAAATACCACGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAA
GGACAAAATCAACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGAC
TCCAGAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTG
CAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACAC
TTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCAT
GCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCT
CCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCC
GTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTG
CCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACT
TGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTG
TAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTAC
AGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTG
AGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCC
GAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGC
CAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGA
ATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTT
GCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAG
TTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGT
GAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATC
TGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCG
CTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTG
ATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAG
TGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGT
CTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCT
CACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTG
TCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGG
CCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGC
ACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACG
GGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGT
CACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGC
AGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAG
ATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCA
GTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGA
GGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGG
GTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTT
ACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTA
AATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTC
GTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAA
ATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTA
TTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTG
ATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAA
AATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352933 ⟹ NP_001339862

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGTCATTAACAGCTGAAGAGAAGAC
GATTACAGAAAAGCACCTTGAATTATGCCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGC
ACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGA
CACTTTCTCAGTTACAGAGAGATGAATTACAGTTTATCGACTGGGAGATTGACAGTGACAGGGC
AGAGGCTAGTGACTGTGATGAATTTGAAGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCT
TCTTGTGCAAGTAATCAGTCTTTGACAAGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTT
CTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACT
CATTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGGATGCAAGACAGATTATG
GAGAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCATACACCTCAGAAACCCA
CAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGC
AGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGT
ATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGC
TGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAG
CTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACT
GCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGA
TTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAA
AGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATC
TCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGT
GTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCAT
CCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCG
TGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCA
CCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCT
GGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGA
CAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAA
GGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACC
TGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATC
CTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTT
ACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTG
CAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAA
AGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGC
TCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGC
ACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATT
GTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAA
GTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTC
CATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTG
TGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTG
GGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTG
CCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTG
AGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGT
TGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAAT
CGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAACT
TTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTATG
GACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAGA
TACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAAA
TTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTTA
GGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTACC
ATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTAA
ACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTGC
AGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAAA
GTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352934 ⟹ NP_001339863

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAG
ATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATA
CCACGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAA
TCAACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAA
ATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCG
AGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGT
AGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTG
CCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCC
TGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAG
GACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTA
TTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGT
GTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAG
GGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAG
CCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTC
TCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTG
GTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAG
GACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGG
TGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTG
GTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTG
ACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGAT
AAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAA
ATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAA
GAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCA
AAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGAT
GTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGG
CCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCT
CTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTG
CTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGA
TGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGT
TGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTG
GAACAGAGGCCGGAAGACAGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTT
AAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAG
CTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGC
AATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACA
CAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACA
GTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTA
GGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCA
ATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTACCATGA
TTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCT
TTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTT
CACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAAAGTGT
AGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352935 ⟹ NP_001339864

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGC
TCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAATTAC
AGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGAAGA
TGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACAAGT
GATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATA
GTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCA
CGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCA
ACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATT
CAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGA
GAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGA
AAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCA
TGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGG
AGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGAC
ACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTC
TGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTA
CTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGT
CTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCT
GGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCT
CCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTG
CAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGAC
ACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGA
AGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTG
GGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACA
CCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAA
AACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATT
GATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAG
ACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAA
ACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTC
ACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCC
CCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTT
CTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTT
CAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGC
TCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGG
CGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAA
CAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTG
TTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGT
CAAGGTAGGAGCCAGGCCAGAGCACGCACGCACTCCTAGCTCACTCCAACATAGCGAAGCTGTT
GCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAG
AGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGA
CCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTA
GCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGAT
TTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTT
AGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTA
CAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAA
GTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTA
ATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCC
CCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAA
TAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTAT
CACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352936 ⟹ NP_001339865

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGC
TCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAATTAC
AGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGAAGA
TGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACAAGT
GATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATA
GTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCA
CGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCA
ACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATT
CAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGA
GAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGA
AAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCA
TGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGG
AGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGAC
ACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTC
TGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTA
CTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGT
CTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCT
GGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCT
CCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTG
CAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGAC
ACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGA
AGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTG
GGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACA
CCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAA
AACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATT
GATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAG
ACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAA
ACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTC
ACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCC
CCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTT
CTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTT
CAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGC
TCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGAGCTACGAAGTGA
AGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCC
GACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACAC
TAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTG
ATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAAC
TTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTC
TACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTT
AAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTG
TAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTC
CCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTAC
AATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGT
ATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352937 ⟹ NP_001339866

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGTCATTAACAGCTGAAGAGAAGAC
GATTACAGAAAAGCACCTTGAATTATGCCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGC
ACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGA
CACTTTCTCAGTTACAGAGAGATGAATTACAGTTTATCGACTGGGAGATTGACAGTGACAGGGC
AGAGGCTAGTGACTGTGATGAATTTGAAGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCT
TCTTGTGCAAGTAATCAGTCTTTGACAAGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTT
CTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACT
CATTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGGATGCAAGACAGATTATG
GAGAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCATACACCTCAGAAACCCA
CAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGC
AGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGT
ATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGC
TGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAG
CTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACT
GCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGA
TTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAA
AGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATC
TCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGT
GTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCAT
CCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCG
TGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCA
CCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCT
GGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGA
CAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAA
GGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACC
TGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATC
CTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTT
ACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTG
CAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAA
AGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGC
TCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGC
ACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATT
GTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAA
GTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTC
CATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTG
TGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGCTACGAAGTGAAGAG
TGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACC
AGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGC
GGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTT
GGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAG
ATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACA
GTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGT
TTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAAT
TTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCC
AAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATA
AATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCA
CAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352938 ⟹ NP_001339867

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGTCATTAACAGCTGAAGAGAAGAC
GATTACAGAAAAGCACCTTGAATTATGCCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGC
ACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGA
CACTTTCTCAGTTACAGAGAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATAGTGAAA
AAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCACGTGCA
GTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCAACAGAG
ACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAA
AGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATC
TGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCT
GGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTG
AGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGG
CCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTC
CGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATA
CTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCC
GGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACA
AATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCC
ATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGA
TGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGA
GTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAG
ACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCA
CTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATG
AAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGT
GGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCA
TCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATA
ATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTC
TCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACA
GCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTG
CAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGT
GTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAA
GGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAG
CCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACA
GCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGA
CGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGG
CCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCA
AGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCT
GTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTG
AAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACC
CGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACA
CTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGT
GATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAA
CTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTT
CTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCT
TAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTT
GTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATT
CCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTA
CAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTG
TATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352939 ⟹ NP_001339868

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGC
TCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGCCAAGTTCT
ATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCA
TTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGGATGCAAGACAGATTATGGA
GAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCATACACCTCAGAAACCCACA
GCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAG
AAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTAT
TTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTG
CATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCT
CCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGC
AGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATT
ATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAG
AAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTC
TTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGT
AGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCC
CAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTG
GCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACC
AGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGG
TACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACA
GTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGG
ACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTG
GCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCT
CACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTTAC
CAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCA
GTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAG
GGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTC
CCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCAC
TCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGT
TTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGT
TCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCA
TCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTG
TGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGG
GACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCC
GCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAG
GTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTG
TTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAATCG
AGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTT
GCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGA
CACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATA
CAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATT
TAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGG
CAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTACCAT
GATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTAAAC
CTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTGCAG
TTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAAAGT
GTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352940 ⟹ NP_001339869

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGCCAAGT
TCTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTAC
TCATTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGGATGCAAGACAGATTAT
GGAGAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCATACACCTCAGAAACCC
ACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAG
CAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATG
TATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAG
CTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCA
GCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGAC
TGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTG
ATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCA
AAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCAT
CTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTG
TGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCA
TCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTC
GTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGC
ACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTC
TGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAG
ACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGA
AGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACAC
CTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACAT
CCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTT
TACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTT
GCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCA
AAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGG
CTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGG
CACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGAT
TGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCA
AGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACT
CCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGT
GTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGT
GGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACT
GCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTGCT
GAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGG
TTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAA
TCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAAC
TTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTAT
GGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAG
ATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAA
ATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTT
AGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTAC
CATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTA
AACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTG
CAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAA
AGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352941 ⟹ NP_001339870

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGGTAGAA
AATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCAT
GTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGA
GCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACA
CTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCT
GAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTAC
TGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTC
TAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTG
GACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTC
CTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGC
AAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACA
CACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAA
GTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGG
GAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACAC
CCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAA
ACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTG
ATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGA
CATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAA
CCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCA
CTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCC
CTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTC
TTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTC
AGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCT
CGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGC
GTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAAC
AGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGT
TCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTC
AAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACG
AAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGC
CCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCA
GAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTG
GTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAA
TGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACC
TTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTG
AATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTT
CATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTA
ACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTC
TGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGG
AACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352942 ⟹ NP_001339871

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAAACCACCACATCT
AAAAGCACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTGGAAGTGATTTGTCGGATGAAG
ATAAGACACTTTCTCAGTTACAGAGAGATGAATTACAGTTTATCGACTGGGAGATTGACAGTGA
CAGGGCAGAGGCTAGTGACTGTGATGAATTTGAAGATGACGAGGGTGCTGTGGAAATCTCAGAC
TGTGCTTCTTGTGCAAGTAATCAGTCTTTGACAAGTGATGAGAAGCTGTCGGAGCTTCCCAAGC
CAAGTTCTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGATTTGGAAAATGT
CCTACTCATTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGGATGCAAGACAG
ATTATGGAGAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCATACACCTCAGA
AACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGG
ACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACAT
CAATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTT
TAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGC
CACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAG
GAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAA
AACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGT
TGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGA
AGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGG
TTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACA
GCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCT
GCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAG
ACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTG
CCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAG
GCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCA
GAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAA
AACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGT
TACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATA
AGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTAC
CCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTG
GAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACC
CCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCT
GGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGT
CGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTG
GTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGT
CAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGG
CCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTT
CCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCT
GGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCC
CTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAG
TGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGA
GGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTG
TGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTA
ACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATG
TTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTC
TGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGG
TATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACAT
TTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAA
GTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCA
CTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACC
CATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352943 ⟹ NP_001339872

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGCCAAGT
TCTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTAC
TCATTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGGATGCAAGACAGATTAT
GGAGAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCATACACCTCAGAAACCC
ACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAG
CAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATG
TATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAG
CTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCA
GCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGAC
TGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTG
ATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCA
AAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCAT
CTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTG
TGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCA
TCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTC
GTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGC
ACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTC
TGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAG
ACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGA
AGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACAC
CTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACAT
CCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTT
TACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTT
GCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCA
AAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGG
CTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGG
CACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGAT
TGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCA
AGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACT
CCATCTGCAGTGTTCAAGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAA
ATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCT
TCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAA
TGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACA
GTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGT
TTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGG
AACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAAT
ATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTACCATGATT
GAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTT
GTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCA
CTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAG
CTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352944 ⟹ NP_001339873

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGGTAGAA
AATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCAT
GTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGA
GCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACA
CTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCT
GAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTAC
TGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTC
TAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTG
GACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTC
CTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGC
AAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACA
CACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAA
GTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGG
GAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACAC
CCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAA
ACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTG
ATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGA
CATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAA
CCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCA
CTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCC
CTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTC
TTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTC
AGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCT
CGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGAGCTACGAAGTGAA
GAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCG
ACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACT
AGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGA
TTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACT
TAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCT
ACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTA
AGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGT
AATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCC
CCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACA
ATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTA
TCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352945 ⟹ NP_001339874

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGC
TCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGGTAGAAAAT
CTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTG
TGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCT
GGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTG
TCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAA
TACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGT
CCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAA
CAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGAC
CCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTG
GATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAA
GAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACAC
AGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTG
CACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAA
TGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCT
GTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACT
CATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATA
TAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACAT
TCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCA
CAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTC
TGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTT
GTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTC
AAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGA
AGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGA
CAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTG
GACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGA
GGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCT
CAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAG
CTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAG
TGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCA
CCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAA
CACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTG
GTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGA
AACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTT
TTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAAT
CTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCAT
TTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACA
TTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGC
TACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAAC
TGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352946 ⟹ NP_001339875

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGTCATTAACAGCTGAAGAGAAGAC
GATTACAGAAAAGCACCTTGAATTATGCCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGC
ACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGA
CACTTTCTCAGTTACAGAGAGATGAATTACAGTTTATCGACTGGGAGATTGACAGTGACAGGGC
AGAGGCTAGTGACTGTGATGAATTTGAAGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCT
TCTTGTGCAAGTAATCAGTCTTTGACAAGTGATGAGAAGCTGTCGGAGCTTCCCAAGAGGTGGA
CTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATC
AATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTT
AGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCC
ACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGG
AGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAA
ACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTT
GCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAA
GCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGT
TGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAG
CGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTG
CCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGA
CAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGC
CTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGG
CAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAG
AGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAA
ACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTT
ACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAA
GCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACC
CGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGG
AGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCC
CAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTG
GAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTC
GGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGG
TGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTC
AACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGC
CTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTC
CTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTG
GACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCC
TGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGT
GGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAG
GAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGT
GAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAA
CTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGT
TCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCT
GCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGT
ATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATT
TTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAG
TGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCAC
TTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCC
ATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352947 ⟹ NP_001339876

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGTCATTAACAGCTGAAGAGAAGAC
GATTACAGAAAAGCACCTTGAATTATGCCCTAGACCCAAGCAAGCTCGTCCCTCTGTTCGGGGT
CCCTGACTTCCTGCAACACTTAAGTTTCTTAAACCACCACATCTAAAAGCACCAGTGGGCTTAC
AGACATAACATGGAGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTA
CAGAGAGATGAATTACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACT
GTGATGAATTTGAAGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAA
TCAGTCTTTGACAAGTGATGAGAAGCTGTCGGAGCTTCCCAAGAGGTGGACTAGCAGAAAGACT
AAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTAC
CAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGG
AATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCA
AAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTAC
CTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAA
GTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTC
AGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCC
CAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTG
TAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAG
CACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGA
GCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTC
AGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGA
TGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAA
GGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGG
GGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGA
CCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCT
CATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTC
CAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTA
TGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATC
TGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAA
CCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGG
GGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCT
GAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTG
AGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAG
TGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATG
TGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCT
CCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAG
ACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCC
GCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATT
GTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCT
GAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGT
GGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTG
AACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTT
GTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAAC
ATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATA
TGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAA
CATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTC
CCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTA
CTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTC
TCTGAA

hide sequence

RefSeq Acc Id:

NM_001352948 ⟹ NP_001339877

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAG
AATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTT
CAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCA
AGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCC
AGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTC
CCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCC
TGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGT
GAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAA
TTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGG
GACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGG
GATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAG
TGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAG
CTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATG
TTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCA
GCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTT
GATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAA
GAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGG
GACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTG
CTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATT
TACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGA
CCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTA
TGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCAC
AGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCC
TCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCC
GGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACT
GTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGA
GATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCAC
ATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGA
GTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATG
GGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTC
CGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGG
GCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTG
GTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACG
ATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAAT
CAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTT
TTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATT
TTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTA
CAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATA
TTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAAT
GTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352949 ⟹ NP_001339878

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGTGTGCCTGATAGAAGGTGACTACCCAAGCAGTTT
TTTTGACGAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGAT
TTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGG
ATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCA
TACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTT
TTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTT
TGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAAC
TGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTG
GGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTC
TCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCC
TCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGT
GAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCC
TTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACC
TGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAA
GAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAA
GCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCT
TCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGA
ACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCA
CCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACA
GAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCG
ATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTC
CAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGA
CCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAAT
GATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTC
TGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGA
GGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGC
TCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCC
GTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAG
TGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCT
GCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTG
CTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAG
AGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTG
CAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGGTAGGAGCCAGGC
CAGAGCACGCACGCACTCCTAGCTCACTCCAACATAGCGAAGCTGTTGCAGCGCAGCATTTCCT
CCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGA
AGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTG
GAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATC
TGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGT
TAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAA
TGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTT
TCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTT
GGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAAC
ATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCA
AAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAG
CACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTA
CCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352950 ⟹ NP_001339879

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGCCAAGT
TCTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTAC
TCATTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGGATGCAAGACAGATTAT
GGAGAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCATACACCTCAGAAACCC
ACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAG
CAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATG
TATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAG
CTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCA
GCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGAC
TGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTG
ATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCA
AAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCAT
CTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTG
TGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCA
TCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTC
GTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGC
ACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTC
TGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAG
ACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGA
AGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACAC
CTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACAT
CCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTT
TACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTT
GCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCA
AAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGG
CTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGG
CACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGAT
TGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCA
AGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACT
CCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGT
GTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGCTACGAAGTGAAGA
GTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGAC
CAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAG
CGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATT
TGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTA
GATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTAC
AGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAG
TTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAA
TTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCC
CAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAAT
AAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATC
ACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352951 ⟹ NP_001339880

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAG
AATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTT
CAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCA
AGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCC
AGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTC
CCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCC
TGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGT
GAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAA
TTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGG
GACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGG
GATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAG
TGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAG
CTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATG
TTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCA
GCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTT
GATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAA
GAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGG
GACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTG
CTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATT
TACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGA
CCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTA
TGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCAC
AGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCC
TCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCC
GGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACT
GTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGA
GATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCAC
ATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGA
GTGAAGGTCAAGGTAGGAGCCAGGCCAGAGCACGCACGCACTCCTAGCTCACTCCAACATAGCG
AAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACG
AAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGC
CCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCA
GAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTG
GTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAA
TGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACC
TTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTG
AATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTT
CATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTA
ACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTC
TGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGG
AACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352952 ⟹ NP_001339881

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGAGGTGG
ACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACAT
CAATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTT
TAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGC
CACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAG
GAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAA
AACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGT
TGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGA
AGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGG
TTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACA
GCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCT
GCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAG
ACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTG
CCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAG
GCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCA
GAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAA
AACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGT
TACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATA
AGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTAC
CCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTG
GAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACC
CCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCT
GGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGT
CGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTG
GTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGT
CAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGG
CCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTT
CCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCT
GGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCC
CTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAG
TGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGA
GGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTG
TGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTA
ACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATG
TTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTC
TGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGG
TATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACAT
TTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAA
GTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCA
CTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACC
CATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352953 ⟹ NP_001339882

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGC
TCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAATTAC
AGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGAAGA
TGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACAAGT
GATGAGAAGCTGTCGGAGCTTCCCAAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGA
GCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACC
AGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGA
CTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACT
GATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCC
AAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCA
TCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGT
GTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGC
ATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCT
CGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAG
CACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTT
CTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAA
GACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGG
AAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACA
CCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACA
TCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCT
TTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGT
TGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGC
AAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAG
GCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAG
GCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGA
TTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGC
AAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAAC
TCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTG
TGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTG
TGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGAC
TGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTGC
TGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGG
GTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAA
ATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAA
CTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTA
TGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCA
GATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCA
AATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATT
TAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTA
CCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGT
AAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTT
GCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATA
AAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352955 ⟹ NP_001339884

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTT
AGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCC
ACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGG
AGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAA
ACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTT
GCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAA
GCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGT
TGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAG
CGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTG
CCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGA
CAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGC
CTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGG
CAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAG
AGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAA
ACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTT
ACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAA
GCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACC
CGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGG
AGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCC
CAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTG
GAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTC
GGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGG
TGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTC
AACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGC
CTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTC
CTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTG
GACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCC
TGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGT
GGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAG
GAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGT
GAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAA
CTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGT
TCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCT
GCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGT
ATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATT
TTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAG
TGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCAC
TTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCC
ATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352956 ⟹ NP_001339885

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGC
TCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGAGGTGGACT
AGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAA
TGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAG
AGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCAC
CAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAG
ACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAAC
TGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGC
CAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGC
ATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTG
TGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCG
CATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCC
TCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACA
GCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCT
TCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCA
AGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAG
GAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAAC
ACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTAC
ATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGC
TTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCG
TTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAG
CAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCA
GGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGA
GGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGG
ATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTG
CAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAA
CTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCT
GTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCT
GTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGA
CTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTG
CTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGG
GGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGA
AATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGA
ACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACT
ATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTC
AGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGC
AAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTAT
TTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTT
ACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTG
TAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTT
TGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCAT
AAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352957 ⟹ NP_001339886

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTT
AGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCC
ACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGG
AGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAA
ACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTT
GCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAA
GCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGT
TGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAG
CGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTG
CCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGA
CAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGC
CTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGG
CAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAG
AGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAA
ACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTT
ACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAA
GCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACC
CGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGG
AGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCC
CAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTG
GAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTC
GGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGG
TGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTC
AACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGC
CTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGCTACGAAGTG
AAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACC
CGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACA
CTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGT
GATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAA
CTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTT
CTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCT
TAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTT
GTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATT
CCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTA
CAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTG
TATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352958 ⟹ NP_001339887

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGTGTGCCTGATAGAAGGTGACTACCCAAGCAGTTT
TTTTGACGAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGAT
TTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGG
ATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCA
TACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTT
TTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTT
TGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAAC
TGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTG
GGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTC
TCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCC
TCCCTGGCAAAAAGAATTAATAGAAAATGGCAGCCCAAGAGGCAAAAACTGATTATTCCAAGTG
GAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGA
AAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAG
ATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAG
CCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCAC
TCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCT
GGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGC
AGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGC
CTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGG
AAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGA
TTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCA
GCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCAT
CCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAG
TTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGC
CACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGG
CTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCC
TGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGC
TGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAA
CGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGC
TGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGT
TCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGT
GGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCC
GGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACC
GCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCC
GGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTT
TTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAG
TGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGC
TGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAAC
GTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTG
AACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATA
TTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGA
GAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACAT
GTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCA
TACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTT
TTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCT
GAA

hide sequence

RefSeq Acc Id:

NM_001352959 ⟹ NP_001339888

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,654,088 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	48,029,802 - 48,111,718 (+)	NCBI

Sequence:

show sequence

ACCATGTGTGTACCAAGAGGCATGCAGGAGCCATTGGGATACTCCCAAAGTTCTCTGGCCAGAG
CCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTC
GAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTC
ACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTC
TGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTT
GTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATT
TATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTG
GTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCT
TCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGA
GACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAG
TCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCA
GGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTC
TCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACAC
CTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTC
ATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCC
TTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCT
TCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTC
CTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAG
GAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGAT
TGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGA
TCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTT
GTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGA
AATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTAT
TTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCAT
TTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGA
ACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTG
CAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTA
AGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGT
TACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352960 ⟹ NP_001339889

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,659,664 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	48,035,380 - 48,111,718 (+)	NCBI

Sequence:

show sequence

TTTTCTCAGCGGCTCCCTTGCGCTCAGGCCTCACCCTCATGGCTCAGAAATGCACAGAATCAAA
GTCCTGCGGAATGGCAGCTGATGGCTGAAACAGGTGAAGGAAACCAAGATTTTGAGCACAGAAG
AGATGCAGGCACTTAACTGGGTGTGAAACAAATTCACATAATCTGGATTGTGCAGAGCCTGCCT
TCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCA
AGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAG
GAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAAC
ACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTAC
ATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGC
TTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCG
TTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAG
CAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCA
GGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGA
GGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGG
ATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTG
CAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAA
CTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCT
GTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCT
GTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGA
CTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTCCCTG
CTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGG
GGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGA
AATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGA
ACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACT
ATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTC
AGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGC
AAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTAT
TTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTT
ACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTG
TAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTT
TGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTACCCAT
AAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NM_001352961 ⟹ NP_001339890

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAG
ATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATA
CCACGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAA
TCAACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAA
ATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCG
AGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGT
AGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTG
CCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCC
TGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAG
GACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTA
TTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGT
GTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAG
GGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAG
CCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTC
TCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTG
GTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAG
GACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGG
TGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTG
GTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTG
ACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGAT
AAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAA
ATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAA
GAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCA
AAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGAT
GTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGG
CCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCT
CTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTG
CTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGA
TGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGAGCTACGAAG
TGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCA
CCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAA
CACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTG
GTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGA
AACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTT
TTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAAT
CTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCAT
TTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACA
TTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGC
TACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAAC
TGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NR_104581

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
HuRef	8	43,638,756 - 44,111,478 (+)	NCBI
CHM1_1	8	48,225,078 - 48,700,450 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTT
AGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCC
ACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGG
AGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAA
ACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTT
GCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAA
GCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGAG
CCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTC
GAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTC
ACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTC
TGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTT
GTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATT
TATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTG
GTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCT
TCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGA
GACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAG
TCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCA
GGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTC
TCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACAC
CTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTC
ATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCC
TTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCT
TCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTC
CTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAG
GAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGAT
TGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGA
TCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTT
GTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGA
AATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTAT
TTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCAT
TTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGA
ACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTG
CAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTA
AGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGT
TACCCATAAAGTGTAGCTCTCTGAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NR_148202

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAG
ATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATA
CCACGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAA
TCAACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAA
ATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCG
AGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGT
AGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTG
CCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCC
TGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAG
GACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTA
TTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGT
GTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAG
GGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAG
CCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTC
TCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTG
GTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAG
GACACACAGACCCAGCTGGAACTCGACGGAGCCTCGCTCTATCGCCCAGGCTGGAGTGCAGTGG
CACGATCTCAGCTCTCTGCAACCTCCACTTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCC
CAAGTAGCTGGAACTACAGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGT
GCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGA
ATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCC
TGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAAC
TCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGAT
ATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACA
TTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACC
ACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACT
CTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCT
TGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTT
CAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAG
AAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCG
ACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGT
GGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAG
AGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTC
TCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAA
GCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAA
GTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCC
ACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGA
ACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGT
GGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATG
AAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTT
TTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAA
TCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCA
TTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAAC
ATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTG
CTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAA
CTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NR_148203

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGTCATTAACAGCTGAAGAGAAGAC
GATTACAGAAAAGCACCTTGAATTATGCCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGC
ACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGA
CACTTTCTCAGTTACAGAGAGATGAATTACAGTTTATCGACTGGGAGATTGACAGTGACAGGGC
AGAGGCTAGTGACTGTGATGAATTTGAAGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCT
TCTTGTGCAAGTAATCAGTCTTTGACAAGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTT
CTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACT
CATTGATTCAGAATCCCCTCACAAATACCACGTGCAGTTTGCATCGGATGCAAGACAGATTATG
GAGAGACTGATAGATCCAAGGACAAAATCAACAGAGACCATTTTGCATACACCTCAGAAACCCA
CAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGC
AGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGT
ATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGC
TGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAG
CTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACT
GCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGA
TTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAA
AGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATC
TCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGT
GTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCAT
CCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCG
TGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCA
CCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCT
GGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGA
CAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAA
GGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACC
TGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATC
CTCACAGCTCATCCAAATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTT
ACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTG
CAGTTTCTATGCCACGGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAA
AGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGC
TCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGC
ACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATT
GTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAA
GTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTC
CATCTGCAGTGTTCAAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTG
TTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGT
CAAGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTAC
GAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCG
CCCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGC
AGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGT
GGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAA
ATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATAC
CTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATT
GAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGT
TCATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTT
AACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTT
CTGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGG
GAACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NR_148204

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAG
ATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATA
CCACGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAA
TCAACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAA
ATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCG
AGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGT
AGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTG
CCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCC
TGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAG
GACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTA
TTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGT
GTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAG
GGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAG
CCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTC
TCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTG
GTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAG
GACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGG
TGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTG
GTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGCGGGGATTTTCAGTTTGATTGACACC
CTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAA
CTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGA
TATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGAC
ATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAAC
CACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCAC
TCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCC
TTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCT
TCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCA
GAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTC
GACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCG
TGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACA
GAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTT
CTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCA
AGCTGTTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGA
AGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCC
CACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAG
AACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGG
TGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAAT
GAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCT
TTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGA
ATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTC
ATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAA
CATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCT
GCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGA
ACTGTATCACAGGTGAAACTGTTACCCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

NR_148205

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,001 (+)	NCBI
T2T-CHM13v2.0	8	47,636,640 - 48,111,718 (+)	NCBI

Sequence:

show sequence

AATGGCAGGGCGCGGTGCGGCGCGCCGAGGTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTC
AGGCGGCGCTCCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTG
GAATACAGAATGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGG
ACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACA
CTTCTGGGAATCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATG
CCCTAGACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGG
AGCTCCAGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAAT
TACAGTTTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGA
AGATGACGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACA
AGTGATGAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAG
ATAGTGAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATA
CCACGTGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAA
TCAACAGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAA
ATTCAGCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCG
AGAGAGATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGT
AGAAAATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTG
CCATGTGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCC
TGGAGCTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAG
GACACTGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTA
TTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGT
GTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAG
GGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAG
CCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTC
TCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTG
GTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAG
GACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGG
TGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTG
GTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTG
ACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGAT
AAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAA
ATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAA
GAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCA
AAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGAT
GTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGG
CCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCT
CTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTG
CTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGA
TGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGAGGCGCCTTT
TCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCC
TGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTGTTGCAGCGCAGCATTTCCTC
CCTGCTGAGGTTTGCCGCCGGTGAAGATGGGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAA
GTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGG
AGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCT
GTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTT
AACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAAT
GTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTT
CTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTG
GTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACA
TTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAA
AGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGC
ACTTTGCAGTTCACTACTTTTGGGAAAATGTTCTAGGGAACTGTATCACAGGTGAAACTGTTAC
CCATAAAGTGTAGCTCTCTGAA

hide sequence

RefSeq Acc Id:

XM_011517497 ⟹ XP_011515799

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI

Sequence:

show sequence

CCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTGGAATACAGAA
TGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGGACAGCAGGGG
CAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACACTTCTGGGAA
TCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATGCCCTAGACCC
AAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTG
GAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAATTACAGTTTAT
CGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGAAGATGACGAG
GGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACAAGTGATGAGA
AGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAA
AGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCACGTGCAG
TTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCAACAGAGA
CCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAA
GAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCT
GCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTG
GTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGA
GCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGC
CTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCC
GGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATAC
TTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCG
GACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAA
ATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCA
TGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGAT
GTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAG
TGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGA
CCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCAC
TTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGA
AGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTG
GCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCAT
CTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAA
TTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCT
CCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAG
CTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGC
AAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTG
TGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAG
GACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGC
CCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAG
CCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGAC
GAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGC
CGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAA
GAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGCTG
TTGCAGCGCAGCATTTCCTCCCTGCTGAGGTTTGCCGCCGGTGAAGATGGGCTCTATTCACAGT
GGCTGATCAGGTCTTTACTGCGGATCTGGAAAGAAGCTGATAGAAGATGGGTGCCAGAGGGGCC
TGGGTAGAGATGTTAGCTGAGAGATACCCAGTATGGATTCTGTCAGTTTTCTGGAGCTACGAAG
TGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCA
CCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAA
CACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTG
GTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGA
AACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTT
TTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAAT
CTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCAT
TTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACA
TTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGC
TACAATAAATGTCAAACCTAAGCACTTTGCAGTTCA

hide sequence

RefSeq Acc Id:

XM_017013268 ⟹ XP_016868757

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI

Sequence:

show sequence

CCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTGGAATACAGAA
TGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGGACAGCAGGGG
CAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACACTTCTGGGAA
TCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATGCCCTAGACCC
AAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTG
GAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAATTACAGTTTAT
CGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGAAGATGACGAG
GGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACAAGTGATGAGA
AGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAA
AGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCACGTGCAG
TTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCAACAGAGA
CCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAA
GAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCT
GCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTG
GTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGA
GCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGC
CTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCC
GGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATAC
TTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCG
GACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAA
ATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCA
TGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGAT
GTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAG
TGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGA
CCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCAC
TTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGA
AGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTG
GCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCAT
CTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAA
TTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCT
CCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACCACAG
CTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACTCTGC
AAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCTTGTG
TGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTTCAAG
GACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAGAAGC
CCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCGACAG
CCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGTGGAC
GAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAGAGGC
CGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTCTCAA
GAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAAGGTA
GGAGCCAGGCCAGAGCACGCACGCACTCCTAGCTCACTCCAACATAGCGAAGAGCTACGAAGTG
AAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCCCACC
CGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAGAACA
CTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGGTGGT
GATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAATGAAA
CTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCTTTTT
CTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGAATCT
TAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTCATTT
GTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAACATT
CCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCTGCTA
CAATAAATGTCAAACCTAAGCACTTTGCAGTTCA

hide sequence

RefSeq Acc Id:

XM_017013269 ⟹ XP_016868758

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI

Sequence:

show sequence

CCCGGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTGGAATACAGAA
TGCCCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGGACAGCAGGGG
CAGCTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACACTTCTGGGAA
TCCGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATGCCCTAGACCC
AAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTG
GAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAATTACAGTTTAT
CGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGAAGATGACGAG
GGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACAAGTGATGAGA
AGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATAGTGAAAA
AGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCACGTGCAG
TTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCAACAGAGA
CCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAGCAAA
GAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCT
GCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAATCTG
GTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGTGTGA
GCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGCTGGC
CTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACTGTCC
GGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGAATAC
TTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTGTCCG
GACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTAACAA
ATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGACCCA
TGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCTGGAT
GTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAAAGAG
TGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACACAGA
CCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGTGCAC
TTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGAATGA
AGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCCTGTG
GCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAACTCAT
CTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGATATAA
TTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACATTCT
CCAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACT
CTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCT
TGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTT
CAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAG
AAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCG
ACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGT
GGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAG
AGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTC
TCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAA
GGTAGGAGCCAGGCCAGAGCACGCACGCACTCCTAGCTCACTCCAACATAGCGAAGAGCTACGA
AGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCC
CACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAG
AACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGG
TGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAAT
GAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACCT
TTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTGA
ATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTTC
ATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTAA
CATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTCT
GCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCA

hide sequence

RefSeq Acc Id:

XM_017013270 ⟹ XP_016868759

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI

Sequence:

show sequence

GGAGATGCCCCGCGGCAGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTGGAATACAGAATGC
CCATCCTTTCCAGGAGAAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGGACAGCAGGGGCAG
CTGCCTCTCTCTCTGAAGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACACTTCTGGGAATCC
GTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATGCCCTAGACCCAAG
CAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTGGAA
GTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGTGTGCCTGATAGAAGGTGA
CTACCCAAGCAGTTTTTTTGACGAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATAGT
GAAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCACG
TGCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCAAC
AGAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATTCA
GCAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGA
GATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAA
ATCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATG
TGTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAG
CTGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACAC
TGTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTG
AATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACT
GTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCT
AACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGG
ACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCC
TGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCA
AAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACAC
ACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAG
TGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGG
AATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACC
CTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAA
CTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGA
TATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGAC
ATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAAC
CACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCAC
TCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCC
TTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCT
TCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCA
GAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTC
GACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCG
TGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACA
GAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTT
CTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCA
AGGTAGGAGCCAGGCCAGAGCACGCACGCACTCCTAGCTCACTCCAACATAGCGAAGAGCTACG
AAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGC
CCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCA
GAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTG
GTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGTAGTTTACGATCTTGAAA
TGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAACTGTAAATCAAAATACC
TTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATTTACTCGTTTTCACATTG
AATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGAAAAAAATTTTTTTTGTT
CATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGTTTTTATTACAGTATTTA
ACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATACTGTGATATTACTGTTC
TGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCA

hide sequence

RefSeq Acc Id:

XM_017013271 ⟹ XP_016868760

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,279,219 - 47,736,306 (+)	NCBI

Sequence:

show sequence

GGGTCTTGTAAAAATATGGCCACTTGTGTATTTGTCTTGTAGATTCTCCCTGACTCTGCTCATC
TGGACCTTTTCTGTGTGTCTGCCACCCCTGTGCTGCTGAGTGGATTCCACTTCCAGTACTTTCT
CAGTGACGGGTCCAGAAGGGAGTCCAGGGTGACCAGTTTCAGGTGGCCCAGGCTGCTCTCATCT
CTTCACATCTTCTTACGAGAAAAAGGAGTTGGAATACAGAATGCCCATCCTTTCCAGGAGAAAG
ACCACTGCAGGTCAGAAGAGCAGGTCTCAGGACAGCAGGGGCAGCTGCCTCTCTCTCTGAAGCA
TGGCTCAGTCATTAACAGCTGAAGAGAAGACGATTACAGAAAAGCACCTTGAATTATGCCCTAG
ACCCAAGCAAGAAACCACCACATCTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGCTCC
AGTGGAAGTGATTTGTCGGATGAAGATAAGACACTTTCTCAGTTACAGAGAGATGAATTACAGT
TTATCGACTGGGAGATTGACAGTGACAGGGCAGAGGCTAGTGACTGTGATGAATTTGAAGATGA
CGAGGGTGCTGTGGAAATCTCAGACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACAAGTGAT
GAGAAGCTGTCGGAGCTTCCCAAGCCAAGTTCTATAGAAATTTTAGAGTATTCATCAGATAGTG
AAAAAGAAGATGATTTGGAAAATGTCCTACTCATTGATTCAGAATCCCCTCACAAATACCACGT
GCAGTTTGCATCGGATGCAAGACAGATTATGGAGAGACTGATAGATCCAAGGACAAAATCAACA
GAGACCATTTTGCATACACCTCAGAAACCCACAGCTAAGTTTCCCAGGACTCCAGAAAATTCAG
CAAAGAAGAAGCTTTTAAGAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAG
ATCTGCTATTTCTTTGTGGAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGTAGAAAA
TCTGGTGTATTAACTGTGAAAATTTTAGAGCTGCATGAGGAATGTGCCATGCAAGTTGCCATGT
GTGAGCAGTTATTGGGGTCACCAGCCACCAGCTCCTCCCAAAGTGTGGCTCCCAGGCCTGGAGC
TGGCCTGAAAGTTCTCTTCACCAAGGAGACTGCAGGCTACCTCAGGGGCCGTCCCCAGGACACT
GTCCGGATCTTCCCTCCCTGGCAAAAACTGATTATTCCAAGTGGAAGTTGCCCTGTTATTCTGA
ATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAAAACTTGTGAAGTGTACTG
TCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATGTTTGTAATTAAGGGTCTA
ACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCACTACAGGGACAGCCTGGA
CCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCCCCTGAGGGATTCTCTCCT
GGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGAGTCCGAGTGGTGGTGCAA
AGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGGGGGCCAGCTCAGGACACA
CAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTGTGGAATGTTCGGTGAAGT
GCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAGTCTTGCAGCCTGGTGGGA
ATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTTTCAGTTTGATTGACACCC
TGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCCCTGTGAAGAGATAAAAAC
TCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCAAATCTGGGACAAATTGAT
ATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTACCCGCTGCTTAAGAGACA
TTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCACGGTGATTTACCAAAAACC
ACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTGCTAGTGACCGATGTCACT
CTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGCTGGTCTATGTGGCCCCCT
TGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGCCCCTCACAGCCTCTTCTT
CAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGAACTGTCCTCTTGCTTCAG
AAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGCCTGGCCCGGTGATGCTCG
ACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCAAGGCACTGTGGTTGGCGT
GGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGCAACGGGAGATTGGAACAG
AGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGGTGGTCACATCTCCTGTTC
TCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCAGTGCAGAGTGAAGGTCAA
GGTAGGAGCCAGGCCAGAGCACGCACGCACTCCTAGCTCACTCCAACATAGCGAAGAGCTACGA
AGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTTGTCCAGTCCGTAACCGCC
CACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTGCAGGAGGGGCCTCTGCAG
AACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTGCAAGGGTGGTGGTGGTGG
TGGTGA

hide sequence

RefSeq Acc Id:

XM_017013273 ⟹ XP_016868762

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI

Sequence:

show sequence

GTGGGACGGCGGCGCGCTGAGGAGGCGGTGCGCTCAGGCGGCGCTCCCGGAGATGCCCCGCGGC
AGCCGCGCTCGGGGCTCTAAGAGAAAAAGGAGTTGGAATACAGAATGCCCATCCTTTCCAGGAG
AAAGACCACTGCAGGTCAGAAGAGCAGGTCTCAGGACAGCAGGGGCAGCTGCCTCTCTCTCTGA
AGCATGGCTCAGGTGTGGAGAAGGGTTTCAGAACACTTCTGGGAATCCGTCATTAACAGCTGAA
GAGAAGACGATTACAGAAAAGCACCTTGAATTATGCCCTAGACCCAAGCAAGAAACCACCACAT
CTAAAAGCACCAGTGGGCTTACAGACATAACATGGAGCTCCAGTGGAAGTGATTTGTCGGATGA
AGATAAGACACTTTCTCAGTTACAGAGAGATGAATTACAGTTTATCGACTGGGAGATTGACAGT
GACAGGGCAGAGGCTAGTGACTGTGATGAATTTGAAGATGACGAGGGTGCTGTGGAAATCTCAG
ACTGTGCTTCTTGTGCAAGTAATCAGTCTTTGACAAGTGATGAGAAGCTGTCGGAGCTTCCCAA
GAGGTGGACTAGCAGAAAGACTAAATGGACTGCAGAATCGAGAGAGATCTGCTATTTCTTTGTG
GAGACATCAATGTATTTCTTACCAAAAGACACTTTCAGGCAAAAACTGATTATTCCAAGTGGAA
GTTGCCCTGTTATTCTGAATACTTACTTTTGTGAGAAAGTTGTTGCCAAAGAAGATTCAGAAAA
AACTTGTGAAGTGTACTGTCCGGACATACCCCTTCCAAGAAGAAGCATCTCTTTGGCCCAGATG
TTTGTAATTAAGGGTCTAACAAATAATTCACCTGAAATCCAGGTTGTGTGTAGTGGTGTAGCCA
CTACAGGGACAGCCTGGACCCATGGGCACAAAGAAGCAAAACAGCGCATCCCAACCAGCACTCC
CCTGAGGGATTCTCTCCTGGATGTGGTGGAAAGCCAGGGAGCTGCCTCGTGGCCAGGAGCTGGA
GTCCGAGTGGTGGTGCAAAGAGTGTATTCTCTTCCCAGCAGAGACAGCACCAGGGGTCAGCAGG
GGGCCAGCTCAGGACACACAGACCCAGCTGGAACTCGAGCCTGCCTTCTGGTACAAGATGCCTG
TGGAATGTTCGGTGAAGTGCACTTGGAGTTCACCATGTCGAAGGCAAGACAGTTGGAAGGGAAG
TCTTGCAGCCTGGTGGGAATGAAGGTTCTACAGAAAGTCACCAGAGGAAGGACAGCGGGGATTT
TCAGTTTGATTGACACCCTGTGGCCCCCAGCGATACCTCTGAAAACACCTGGCCGCGACCAGCC
CTGTGAAGAGATAAAAACTCATCTGCCTCCTCCAGCCTTGTGTTACATCCTCACAGCTCATCCA
AATCTGGGACAAATTGATATAATTGACGAAGACCCCATTTATAAGCTTTACCAGCCTCCAGTTA
CCCGCTGCTTAAGAGACATTCTCCAGATGAATGATCTTGGTACCCGTTGCAGTTTCTATGCCAC
GGTGATTTACCAAAAACCACAGCTGAAGAGTCTGCTGCTTCTGGAGCAAAGGGAGATCTGGCTG
CTAGTGACCGATGTCACTCTGCAAACGAAGGAGGAGAGAGACCCCAGGCTCCCCAAAACCCTGC
TGGTCTATGTGGCCCCCTTGTGTGTGCTGGGCTCTGAAGTCCTGGAGGCACTCGCTGGGGCTGC
CCCTCACAGCCTCTTCTTCAAGGACGCTCTCCGTGACCAGGGTCGGATTGTTTGTGCTGAACGA
ACTGTCCTCTTGCTTCAGAAGCCCCTTTTGAGTGTGGTCTCTGGTGCAAGTTCCTGTGAGCTGC
CTGGCCCGGTGATGCTCGACAGCCTGGACTCTGCAACACCTGTCAACTCCATCTGCAGTGTTCA
AGGCACTGTGGTTGGCGTGGACGAGAGCACTGCTTTCTCATGGCCTGTGTGTGACATGTGTGGC
AACGGGAGATTGGAACAGAGGCCGGAAGACAGAGGCGCCTTTTCCTGTGGGGACTGCTCCCGGG
TGGTCACATCTCCTGTTCTCAAGAGGCACCTGCAGGTCTTCCTGGACTGCCGCTCAAGACCGCA
GTGCAGAGTGAAGGTCAAGGTAGGAGCCAGGCCAGAGCACGCACGCACTCCTAGCTCACTCCAA
CATAGCGAAGAGCTACGAAGTGAAGAGTGTCCTCGGAAAGGAAGTGGGGTTGTTAAATTGTTTT
GTCCAGTCCGTAACCGCCCACCCGACCAGCTGCATTGGATTGGAGGAAATCGAGCTTCTGAGTG
CAGGAGGGGCCTCTGCAGAACACTAGCGGTTGCCGCAGGATCTGTGAACTTTGCAATGTGGCTG
CAAGGGTGGTGGTGGTGGTGGTGATTTGGGGTAGTTATTTGTTAACTATGGACACAGTGAACGT
AGTTTACGATCTTGAAATGAAACTTAGATTTTTCTGGGGAAATGTTCAGATACAGTTTTGTGAA
CTGTAAATCAAAATACCTTTTTCTACAGTTTATCTTTTATTTTCTGCAAATTTAGGAACATATT
TACTCGTTTTCACATTGAATCTTAAGTTTAAGCTCTTCATTTGGTATTTAGGCAATATATGAGA
AAAAAATTTTTTTTGTTCATTTGTAATTTTAACAAGTTGAACATTTTACCATGATTGAACATGT
TTTTATTACAGTATTTAACATTCCCCCAAAGAATACCCTGCAAAGTGTAAACCTTTGTCCCATA
CTGTGATATTACTGTTCTGCTACAATAAATGTCAAACCTAAGCACTTTGCAGTTCA

hide sequence

RefSeq Acc Id:

XM_047421638 ⟹ XP_047277594

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421639 ⟹ XP_047277595

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,729,471 (+)	NCBI

RefSeq Acc Id:

XM_047421640 ⟹ XP_047277596

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,279,227 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421641 ⟹ XP_047277597

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421642 ⟹ XP_047277598

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421643 ⟹ XP_047277599

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421644 ⟹ XP_047277600

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,878 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421645 ⟹ XP_047277601

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,284,028 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421646 ⟹ XP_047277602

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,388,341 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421647 ⟹ XP_047277603

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,330,739 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421648 ⟹ XP_047277604

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,293,893 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421649 ⟹ XP_047277605

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,293,970 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421650 ⟹ XP_047277606

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,284,028 - 47,713,641 (+)	NCBI

RefSeq Acc Id:

XM_047421651 ⟹ XP_047277607

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,491,863 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_047421652 ⟹ XP_047277608

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,542,119 - 47,736,306 (+)	NCBI

RefSeq Acc Id:

XM_054360202 ⟹ XP_054216177

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360203 ⟹ XP_054216178

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360204 ⟹ XP_054216179

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360205 ⟹ XP_054216180

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360206 ⟹ XP_054216181

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360207 ⟹ XP_054216182

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,105,188 (+)	NCBI

RefSeq Acc Id:

XM_054360208 ⟹ XP_054216183

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,654,977 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360209 ⟹ XP_054216184

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,654,985 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360210 ⟹ XP_054216185

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360211 ⟹ XP_054216186

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360212 ⟹ XP_054216187

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360213 ⟹ XP_054216188

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360214 ⟹ XP_054216189

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,636,640 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360215 ⟹ XP_054216190

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,659,787 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360216 ⟹ XP_054216191

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,764,093 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360217 ⟹ XP_054216192

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,706,417 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360218 ⟹ XP_054216193

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,669,652 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360219 ⟹ XP_054216194

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,669,729 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360220 ⟹ XP_054216195

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,859,088 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360221 ⟹ XP_054216196

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,659,787 - 48,089,358 (+)	NCBI

RefSeq Acc Id:

XM_054360222 ⟹ XP_054216197

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,859,134 - 48,112,023 (+)	NCBI

RefSeq Acc Id:

XM_054360223 ⟹ XP_054216198

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	47,917,823 - 48,112,023 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001073863	(Get FASTA)	NCBI Sequence Viewer
	NP_001269845	(Get FASTA)	NCBI Sequence Viewer
	NP_001269848	(Get FASTA)	NCBI Sequence Viewer
	NP_001339860	(Get FASTA)	NCBI Sequence Viewer
	NP_001339861	(Get FASTA)	NCBI Sequence Viewer
	NP_001339862	(Get FASTA)	NCBI Sequence Viewer
	NP_001339863	(Get FASTA)	NCBI Sequence Viewer
	NP_001339864	(Get FASTA)	NCBI Sequence Viewer
	NP_001339865	(Get FASTA)	NCBI Sequence Viewer
	NP_001339866	(Get FASTA)	NCBI Sequence Viewer
	NP_001339867	(Get FASTA)	NCBI Sequence Viewer
	NP_001339868	(Get FASTA)	NCBI Sequence Viewer
	NP_001339869	(Get FASTA)	NCBI Sequence Viewer
	NP_001339870	(Get FASTA)	NCBI Sequence Viewer
	NP_001339871	(Get FASTA)	NCBI Sequence Viewer
	NP_001339872	(Get FASTA)	NCBI Sequence Viewer
	NP_001339873	(Get FASTA)	NCBI Sequence Viewer
	NP_001339874	(Get FASTA)	NCBI Sequence Viewer
	NP_001339875	(Get FASTA)	NCBI Sequence Viewer
	NP_001339876	(Get FASTA)	NCBI Sequence Viewer
	NP_001339877	(Get FASTA)	NCBI Sequence Viewer
	NP_001339878	(Get FASTA)	NCBI Sequence Viewer
	NP_001339879	(Get FASTA)	NCBI Sequence Viewer
	NP_001339880	(Get FASTA)	NCBI Sequence Viewer
	NP_001339881	(Get FASTA)	NCBI Sequence Viewer
	NP_001339882	(Get FASTA)	NCBI Sequence Viewer
	NP_001339884	(Get FASTA)	NCBI Sequence Viewer
	NP_001339885	(Get FASTA)	NCBI Sequence Viewer
	NP_001339886	(Get FASTA)	NCBI Sequence Viewer
	NP_001339887	(Get FASTA)	NCBI Sequence Viewer
	NP_001339888	(Get FASTA)	NCBI Sequence Viewer
	NP_001339889	(Get FASTA)	NCBI Sequence Viewer
	NP_001339890	(Get FASTA)	NCBI Sequence Viewer
	XP_011515799	(Get FASTA)	NCBI Sequence Viewer
	XP_016868757	(Get FASTA)	NCBI Sequence Viewer
	XP_016868758	(Get FASTA)	NCBI Sequence Viewer
	XP_016868759	(Get FASTA)	NCBI Sequence Viewer
	XP_016868760	(Get FASTA)	NCBI Sequence Viewer
	XP_016868762	(Get FASTA)	NCBI Sequence Viewer
	XP_047277594	(Get FASTA)	NCBI Sequence Viewer
	XP_047277595	(Get FASTA)	NCBI Sequence Viewer
	XP_047277596	(Get FASTA)	NCBI Sequence Viewer
	XP_047277597	(Get FASTA)	NCBI Sequence Viewer
	XP_047277598	(Get FASTA)	NCBI Sequence Viewer
	XP_047277599	(Get FASTA)	NCBI Sequence Viewer
	XP_047277600	(Get FASTA)	NCBI Sequence Viewer
	XP_047277601	(Get FASTA)	NCBI Sequence Viewer
	XP_047277602	(Get FASTA)	NCBI Sequence Viewer
	XP_047277603	(Get FASTA)	NCBI Sequence Viewer
	XP_047277604	(Get FASTA)	NCBI Sequence Viewer
	XP_047277605	(Get FASTA)	NCBI Sequence Viewer
	XP_047277606	(Get FASTA)	NCBI Sequence Viewer
	XP_047277607	(Get FASTA)	NCBI Sequence Viewer
	XP_047277608	(Get FASTA)	NCBI Sequence Viewer
	XP_054216177	(Get FASTA)	NCBI Sequence Viewer
	XP_054216178	(Get FASTA)	NCBI Sequence Viewer
	XP_054216179	(Get FASTA)	NCBI Sequence Viewer
	XP_054216180	(Get FASTA)	NCBI Sequence Viewer
	XP_054216181	(Get FASTA)	NCBI Sequence Viewer
	XP_054216182	(Get FASTA)	NCBI Sequence Viewer
	XP_054216183	(Get FASTA)	NCBI Sequence Viewer
	XP_054216184	(Get FASTA)	NCBI Sequence Viewer
	XP_054216185	(Get FASTA)	NCBI Sequence Viewer
	XP_054216186	(Get FASTA)	NCBI Sequence Viewer
	XP_054216187	(Get FASTA)	NCBI Sequence Viewer
	XP_054216188	(Get FASTA)	NCBI Sequence Viewer
	XP_054216189	(Get FASTA)	NCBI Sequence Viewer
	XP_054216190	(Get FASTA)	NCBI Sequence Viewer
	XP_054216191	(Get FASTA)	NCBI Sequence Viewer
	XP_054216192	(Get FASTA)	NCBI Sequence Viewer
	XP_054216193	(Get FASTA)	NCBI Sequence Viewer
	XP_054216194	(Get FASTA)	NCBI Sequence Viewer
	XP_054216195	(Get FASTA)	NCBI Sequence Viewer
	XP_054216196	(Get FASTA)	NCBI Sequence Viewer
	XP_054216197	(Get FASTA)	NCBI Sequence Viewer
	XP_054216198	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH15561	(Get FASTA)	NCBI Sequence Viewer
	BAA09767	(Get FASTA)	NCBI Sequence Viewer
	BAG51554	(Get FASTA)	NCBI Sequence Viewer
	BAG57216	(Get FASTA)	NCBI Sequence Viewer
	BAG57344	(Get FASTA)	NCBI Sequence Viewer
	BAG57544	(Get FASTA)	NCBI Sequence Viewer
	BAG57563	(Get FASTA)	NCBI Sequence Viewer
	BAG60041	(Get FASTA)	NCBI Sequence Viewer
	BAG63150	(Get FASTA)	NCBI Sequence Viewer
	BAG64244	(Get FASTA)	NCBI Sequence Viewer
	BAG64598	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000297423
	ENSP00000297423.4
	ENSP00000427878.1
	ENSP00000427889
	ENSP00000427889.1
	ENSP00000428222.1
	ENSP00000428287.1
	ENSP00000429193
	ENSP00000429193.1
	ENSP00000429448.1
	ENSP00000429487
	ENSP00000429487.1
	ENSP00000429805.1
	ENSP00000429997.1
	ENSP00000430091.1
	ENSP00000430664.1
	ENSP00000430941.1
	ENSP00000430965.1
	ENSP00000444061
	ENSP00000444061.1
GenBank Protein	Q14159	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001073863 ⟸ NM_001080394
- Peptide Label:	isoform 1
- UniProtKB:	B4E0Y6 (UniProtKB/Swiss-Prot), B4DFV2 (UniProtKB/Swiss-Prot), Q96BI5 (UniProtKB/Swiss-Prot), Q14159 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDW EIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKED DLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKK LLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQL LGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYF CEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGH KEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPA GTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPP AIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQM NDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVL GSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLD SATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRH LQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFVQSVTAHPTS CIGLEEIELLSAGGASAEH hide sequence

RefSeq Acc Id:	NP_001269845 ⟸ NM_001282916
- Peptide Label:	isoform 2
- UniProtKB:	Q14159 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAQVWRRVSEHFWESETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDWEIDSDR AEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKEDDLENVL LIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKKLLRGGL AERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPAT SSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYFCEKVVA KEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQR IPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACL LVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKT PGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTR CSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLE ALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLDSATPVN SICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLD CRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFVQSVTAHPTSCIGLEE IELLSAGGASAEH hide sequence

RefSeq Acc Id:	NP_001269848 ⟸ NM_001282919
- Peptide Label:	isoform 3
- UniProtKB:	Q14159 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAQSLTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQ FIDWEIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDS EKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENS AKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAM CEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVIL NTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAW THGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGH TDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDT LWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRD ILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAP LCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVML DSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPV LKRHLQVFLDCRSRPQCRVKVKVGARPEHARTPSSLQHSEELRSEECPRKGSGVVKLFCPVRNR PPDQLHWIGGNRASECRRGLCRTLAVAAGSVNFAMWLQGWWWWW hide sequence

RefSeq Acc Id:	XP_011515799 ⟸ XM_011517497
- Peptide Label:	isoform X5
- UniProtKB:	B4DEV5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDW EIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKED DLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKK LLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQL LGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYF CEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGH KEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPA GTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPP AIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQM NDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVL GSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLD SATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRH LQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGLYSQWLIRSLLRIWKEADRRWVPEGPG hide sequence

RefSeq Acc Id:

XP_016868762 ⟸ XM_017013273

- Peptide Label:

isoform X12

- Sequence:

show sequence

MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS
LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDW
EIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKRWTSRKTKWTAESREIC
YFFVETSMYFLPKDTFRQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSIS
LAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASW
PGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQ
LEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYIL
TAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQR
EIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIV
CAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVC
DMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKVGARPEHARTP
SSLQHSEELRSEECPRKGSGVVKLFCPVRNRPPDQLHWIGGNRASECRRGLCRTLAVAAGSVNF
AMWLQGWWWWW

hide sequence

RefSeq Acc Id:

XP_016868759 ⟸ XM_017013270

- Peptide Label:

isoform X3

- Sequence:

show sequence

MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS
LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRVCLIEGDY
PSSFFDEPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTE
TILHTPQKPTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKS
GVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTV
RIFPPWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLT
NNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQR
VYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGM
KVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDI
IDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTL
QTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQK
PLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQR
PEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKVGARPEHARTPSSLQHSEELRS
EECPRKGSGVVKLFCPVRNRPPDQLHWIGGNRASECRRGLCRTLAVAAGSVNFAMWLQGWWWWW

hide sequence

RefSeq Acc Id:

XP_016868757 ⟸ XM_017013268

- Peptide Label:

isoform X1

- Sequence:

show sequence

MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS
LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDW
EIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKED
DLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKK
LLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQL
LGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYF
CEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGH
KEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPA
GTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPP
AIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQM
NDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVL
GSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLD
SATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRH
LQVFLDCRSRPQCRVKVKVGARPEHARTPSSLQHSEELRSEECPRKGSGVVKLFCPVRNRPPDQ
LHWIGGNRASECRRGLCRTLAVAAGSVNFAMWLQGWWWWW

hide sequence

RefSeq Acc Id:

XP_016868758 ⟸ XM_017013269

- Peptide Label:

isoform X2

- Sequence:

show sequence

MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS
LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDW
EIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKED
DLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKK
LLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQL
LGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYF
CEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGH
KEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPA
GTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPP
AIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQL
KSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKD
ALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDE
STAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKVG
ARPEHARTPSSLQHSEELRSEECPRKGSGVVKLFCPVRNRPPDQLHWIGGNRASECRRGLCRTL
AVAAGSVNFAMWLQGWWWWW

hide sequence

RefSeq Acc Id:	XP_016868760 ⟸ XM_017013271
- Peptide Label:	isoform X7
- UniProtKB:	Q14159 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAQSLTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQ FIDWEIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDS EKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENS AKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAM CEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVIL NTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAW THGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGH TDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDT LWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRD ILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAP LCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVML DSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPV LKRHLQVFLDCRSRPQCRVKVKVGARPEHARTPSSLQHSEELRSEECPRKGSGVVKLFCPVRNR PPDQLHWIGGNRASECRRGLCRTLAVAAGSVNFAMWLQGWWWWW hide sequence

RefSeq Acc Id:	NP_001339887 ⟸ NM_001352958
- Peptide Label:	isoform 24
- UniProtKB:	B4DZY2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MFVIKGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGA GVRVVVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEG KSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAH PNLGQIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIW LLVTDVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAE RTVLLLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMC GNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAA GEDGSYEVKSVLGKEVGLLNCFVQSVTAHPTSCIGLEEIELLSAGGASAEH hide sequence

RefSeq Acc Id:

NP_001339878 ⟸ NM_001352949

- Peptide Label:

isoform 19

- Sequence:

show sequence

MERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQ
CISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKE
TAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRS
ISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAA
SWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKA
RQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCY
ILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLE
QREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGR
IVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWP
VCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKVGARPEHAR
TPSSLQHSEAVAAQHFLPAEVCRR

hide sequence

RefSeq Acc Id:	NP_001339860 ⟸ NM_001352931
- Peptide Label:	isoform 4
- UniProtKB:	B4DEV5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDW EIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKED DLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKK LLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQL LGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYF CEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGH KEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPA GTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPP AIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQM NDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVL GSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLD SATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRH LQVFLDCRSRPQCRVKVKVGARPEHARTPSSLQHSEAVAAQHFLPAEVCRR hide sequence

RefSeq Acc Id:	NP_001339863 ⟸ NM_001352934
- Peptide Label:	isoform 8
- UniProtKB:	B4DEV5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDW EIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKED DLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKK LLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQL LGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYF CEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGH KEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPA GTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPP AIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQM NDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVL GSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLD SATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRATK hide sequence

RefSeq Acc Id:	NP_001339890 ⟸ NM_001352961
- Peptide Label:	isoform 7
- UniProtKB:	B4DEV5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDW EIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKED DLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKK LLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQL LGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYF CEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGH KEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPA GTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPP AIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQM NDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVL GSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLD SATPVNSICSVQELRSEECPRKGSGVVKLFCPVRNRPPDQLHWIGGNRASECRRGLCRTLAVAA GSVNFAMWLQGWWWWW hide sequence

RefSeq Acc Id:

NP_001339880 ⟸ NM_001352951

- Peptide Label:

isoform 21

- Sequence:

show sequence

MRSCRSFPRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQV
AMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPV
ILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGT
AWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASS
GHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLI
DTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCL
RDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYV
APLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPV
MLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTS
PVLKRHLQVFLDCRSRPQCRVKVKVGARPEHARTPSSLQHSEAVAAQHFLPAEVCRR

hide sequence

RefSeq Acc Id:

NP_001339877 ⟸ NM_001352948

- Peptide Label:

isoform 18

- Sequence:

show sequence

MRSCRSFPRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQV
AMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPV
ILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGT
AWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASS
GHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLI
DTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCL
RDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYV
APLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPV
MLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTS
PVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFVQSV
TAHPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:	NP_001339884 ⟸ NM_001352955
- Peptide Label:	isoform 22
- UniProtKB:	H0YBC9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGS CPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVAT TGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQG ASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIF SLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVT RCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLL VYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELP GPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRV VTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFV QSVTAHPTSCIGLEEIELLSAGGASAEH hide sequence

RefSeq Acc Id:	NP_001339886 ⟸ NM_001352957
- Peptide Label:	isoform 23
- UniProtKB:	H0YBC9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGS CPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVAT TGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQG ASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIF SLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVT RCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLL VYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELP GPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRATK hide sequence

RefSeq Acc Id:

NP_001339861 ⟸ NM_001352932

- Peptide Label:

isoform 5

- Sequence:

show sequence

MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS
LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRVCLIEGDY
PSSFFDEPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTE
TILHTPQKPTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKS
GVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTV
RIFPPWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLT
NNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQR
VYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGM
KVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDI
IDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTL
QTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQK
PLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQR
PEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEV
KSVLGKEVGLLNCFVQSVTAHPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:

NP_001339869 ⟸ NM_001352940

- Peptide Label:

isoform 12

- Sequence:

show sequence

MKIRHFLSYREPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRT
KSTETILHTPQKPTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLS
GRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRP
QDTVRIFPPWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVI
KGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRV
VVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCS
LVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLG
QIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVT
DVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVL
LLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGR
LEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDG
SYEVKSVLGKEVGLLNCFVQSVTAHPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:

NP_001339879 ⟸ NM_001352950

- Peptide Label:

isoform 20

- Sequence:

show sequence

MKIRHFLSYREPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRT
KSTETILHTPQKPTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLS
GRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRP
QDTVRIFPPWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVI
KGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRV
VVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCS
LVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLG
QIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVT
DVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVL
LLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGR
LEQRPEDRATK

hide sequence

RefSeq Acc Id:

NP_001339872 ⟸ NM_001352943

- Peptide Label:

isoform 15

- Sequence:

show sequence

MKIRHFLSYREPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRT
KSTETILHTPQKPTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLS
GRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRP
QDTVRIFPPWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVI
KGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRV
VVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCS
LVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLG
QIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVT
DVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVL
LLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQELRSEECPRKGSGVVKLFCPVRNR
PPDQLHWIGGNRASECRRGLCRTLAVAAGSVNFAMWLQGWWWWW

hide sequence

RefSeq Acc Id:	NP_001339881 ⟸ NM_001352952
- Peptide Label:	isoform 22
- UniProtKB:	H0YBC9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGS CPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVAT TGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQG ASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIF SLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVT RCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLL VYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELP GPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRV VTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFV QSVTAHPTSCIGLEEIELLSAGGASAEH hide sequence

RefSeq Acc Id:

NP_001339870 ⟸ NM_001352941

- Peptide Label:

isoform 13

- Sequence:

show sequence

MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS
LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRGRKSGVLT
VKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFP
PWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSP
EIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSL
PSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQ
KVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDED
PIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKE
ERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLS
VVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDR
GAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVL
GKEVGLLNCFVQSVTAHPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:

NP_001339873 ⟸ NM_001352944

- Peptide Label:

isoform 16

- Sequence:

show sequence

MPRGSRARGSKRKRSWNTECPSFPGERPLQVRRAGLRTAGAAASLSEAWLRCGEGFQNTSGNPS
LTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRGRKSGVLT
VKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFP
PWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSP
EIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSL
PSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQ
KVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDED
PIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKE
ERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLS
VVSGASSCELPGPVMLDSLDSATPVNSICSVQELRSEECPRKGSGVVKLFCPVRNRPPDQLHWI
GGNRASECRRGLCRTLAVAAGSVNFAMWLQGWWWWW

hide sequence

RefSeq Acc Id:

NP_001339864 ⟸ NM_001352935

- Peptide Label:

isoform 9

- Sequence:

show sequence

MAQVWRRVSEHFWESETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDWEIDSDR
AEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKEDDLENVL
LIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKKLLRGGL
AERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPAT
SSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYFCEKVVA
KEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQR
IPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACL
LVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKT
PGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTR
CSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLE
ALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLDSATPVN
SICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLD
CRSRPQCRVKVKVGARPEHARTPSSLQHSEAVAAQHFLPAEVCRR

hide sequence

RefSeq Acc Id:	NP_001339865 ⟸ NM_001352936
- Peptide Label:	isoform 10
- UniProtKB:	B4DEV5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQVWRRVSEHFWESETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQFIDWEIDSDR AEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDSEKEDDLENVL LIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKKLLRGGL AERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPAT SSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYFCEKVVA KEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQR IPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACL LVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKT PGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTR CSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLE ALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLDSATPVN SICSVQELRSEECPRKGSGVVKLFCPVRNRPPDQLHWIGGNRASECRRGLCRTLAVAAGSVNFA MWLQGWWWWW hide sequence

RefSeq Acc Id:	NP_001339882 ⟸ NM_001352953
- Peptide Label:	isoform 22
- UniProtKB:	H0YBC9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGS CPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVAT TGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQG ASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIF SLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVT RCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLL VYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELP GPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRV VTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFV QSVTAHPTSCIGLEEIELLSAGGASAEH hide sequence

RefSeq Acc Id:

NP_001339868 ⟸ NM_001352939

- Peptide Label:

isoform 12

- Sequence:

show sequence

MKIRHFLSYREPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRT
KSTETILHTPQKPTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLS
GRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRP
QDTVRIFPPWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVI
KGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRV
VVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCS
LVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLG
QIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVT
DVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVL
LLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGR
LEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDG
SYEVKSVLGKEVGLLNCFVQSVTAHPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:	NP_001339885 ⟸ NM_001352956
- Peptide Label:	isoform 22
- UniProtKB:	H0YBC9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGS CPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVAT TGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQG ASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIF SLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVT RCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLL VYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELP GPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRV VTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFV QSVTAHPTSCIGLEEIELLSAGGASAEH hide sequence

RefSeq Acc Id:

NP_001339874 ⟸ NM_001352945

- Peptide Label:

isoform 17

- Sequence:

show sequence

MAQVWRRVSEHFWESETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRGRKSGVLTVKILEL
HEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLI
IPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVC
SGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDST
RGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGR
TAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLY
QPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRL
PKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGAS
SCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCG
DCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGL
LNCFVQSVTAHPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:

NP_001339876 ⟸ NM_001352947

- Peptide Label:

isoform 18

- Sequence:

show sequence

MRSCRSFPRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQV
AMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPV
ILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGT
AWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASS
GHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLI
DTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCL
RDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYV
APLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPV
MLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTS
PVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFVQSV
TAHPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:

NP_001339862 ⟸ NM_001352933

- Peptide Label:

isoform 6

- Sequence:

show sequence

MAQSLTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQ
FIDWEIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDS
EKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENS
AKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAM
CEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVIL
NTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAW
THGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGH
TDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDT
LWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRD
ILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAP
LCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVML
DSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPV
LKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFVQSVTA
HPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:	NP_001339866 ⟸ NM_001352937
- Peptide Label:	isoform 11
- UniProtKB:	B4DEV5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAQSLTAEEKTITEKHLELCPRPKQETTTSKSTSGLTDITWSSSGSDLSDEDKTLSQLQRDELQ FIDWEIDSDRAEASDCDEFEDDEGAVEISDCASCASNQSLTSDEKLSELPKPSSIEILEYSSDS EKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRTKSTETILHTPQKPTAKFPRTPENS AKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQVAM CEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVIL NTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAW THGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGH TDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDT LWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRD ILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAP LCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVML DSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRATK hide sequence

RefSeq Acc Id:

NP_001339875 ⟸ NM_001352946

- Peptide Label:

isoform 18

- Sequence:

show sequence

MRSCRSFPRGGLAERLNGLQNRERSAISLWRHQCISYQKTLSGRKSGVLTVKILELHEECAMQV
AMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRPQDTVRIFPPWQKLIIPSGSCPV
ILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVIKGLTNNSPEIQVVCSGVATTGT
AWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRVVVQRVYSLPSRDSTRGQQGASS
GHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLI
DTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCL
RDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYV
APLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPV
MLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTS
PVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFVQSV
TAHPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:

NP_001339867 ⟸ NM_001352938

- Peptide Label:

isoform 12

- Sequence:

show sequence

MKIRHFLSYREPSSIEILEYSSDSEKEDDLENVLLIDSESPHKYHVQFASDARQIMERLIDPRT
KSTETILHTPQKPTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQCISYQKTLS
GRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKETAGYLRGRP
QDTVRIFPPWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRSISLAQMFVI
KGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAASWPGAGVRV
VVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKARQLEGKSCS
LVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLG
QIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVT
DVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVL
LLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGR
LEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDG
SYEVKSVLGKEVGLLNCFVQSVTAHPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:

NP_001339871 ⟸ NM_001352942

- Peptide Label:

isoform 14

- Sequence:

show sequence

MERLIDPRTKSTETILHTPQKPTAKFPRTPENSAKKKLLRGGLAERLNGLQNRERSAISLWRHQ
CISYQKTLSGRKSGVLTVKILELHEECAMQVAMCEQLLGSPATSSSQSVAPRPGAGLKVLFTKE
TAGYLRGRPQDTVRIFPPWQKLIIPSGSCPVILNTYFCEKVVAKEDSEKTCEVYCPDIPLPRRS
ISLAQMFVIKGLTNNSPEIQVVCSGVATTGTAWTHGHKEAKQRIPTSTPLRDSLLDVVESQGAA
SWPGAGVRVVVQRVYSLPSRDSTRGQQGASSGHTDPAGTRACLLVQDACGMFGEVHLEFTMSKA
RQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCY
ILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLE
QREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGR
IVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWP
VCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSL
LRFAAGEDGSYEVKSVLGKEVGLLNCFVQSVTAHPTSCIGLEEIELLSAGGASAEH

hide sequence

RefSeq Acc Id:	NP_001339888 ⟸ NM_001352959
- Peptide Label:	isoform 25
- UniProtKB:	B4DWT8 (UniProtKB/TrEMBL), B4DZY2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MCVPRGMQEPLGYSQSSLARACLLVQDACGMFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVT RGRTAGIFSLIDTLWPPAIPLKTPGRDQPCEEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIY KLYQPPVTRCLRDILQMNDLGTRCSFYATVIYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERD PRLPKTLLVYVAPLCVLGSEVLEALAGAAPHSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVS GASSCELPGPVMLDSLDSATPVNSICSVQGTVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAF SCGDCSRVVTSPVLKRHLQVFLDCRSRPQCRVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKE VGLLNCFVQSVTAHPTSCIGLEEIELLSAGGASAEH hide sequence

RefSeq Acc Id:	NP_001339889 ⟸ NM_001352960
- Peptide Label:	isoform 26
- UniProtKB:	B3KP42 (UniProtKB/TrEMBL), B4DZY2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MFGEVHLEFTMSKARQLEGKSCSLVGMKVLQKVTRGRTAGIFSLIDTLWPPAIPLKTPGRDQPC EEIKTHLPPPALCYILTAHPNLGQIDIIDEDPIYKLYQPPVTRCLRDILQMNDLGTRCSFYATV IYQKPQLKSLLLLEQREIWLLVTDVTLQTKEERDPRLPKTLLVYVAPLCVLGSEVLEALAGAAP HSLFFKDALRDQGRIVCAERTVLLLQKPLLSVVSGASSCELPGPVMLDSLDSATPVNSICSVQG TVVGVDESTAFSWPVCDMCGNGRLEQRPEDRGAFSCGDCSRVVTSPVLKRHLQVFLDCRSRPQC RVKVKLLQRSISSLLRFAAGEDGSYEVKSVLGKEVGLLNCFVQSVTAHPTSCIGLEEIELLSAG GASAEH hide sequence

RefSeq Acc Id:

ENSP00000444061 ⟸ ENST00000541342

RefSeq Acc Id:

ENSP00000427889 ⟸ ENST00000517693

RefSeq Acc Id:

ENSP00000427878 ⟸ ENST00000517619

RefSeq Acc Id:

ENSP00000430965 ⟸ ENST00000517824

RefSeq Acc Id:

ENSP00000429487 ⟸ ENST00000518074

RefSeq Acc Id:

ENSP00000429448 ⟸ ENST00000518060

RefSeq Acc Id:

ENSP00000429193 ⟸ ENST00000519401

RefSeq Acc Id:

ENSP00000428287 ⟸ ENST00000519661

RefSeq Acc Id:

ENSP00000297423 ⟸ ENST00000297423

RefSeq Acc Id:

ENSP00000430664 ⟸ ENST00000522222

RefSeq Acc Id:

ENSP00000429805 ⟸ ENST00000522117

RefSeq Acc Id:

ENSP00000428222 ⟸ ENST00000523814

RefSeq Acc Id:

ENSP00000430091 ⟸ ENST00000524006

RefSeq Acc Id:

ENSP00000429997 ⟸ ENST00000524033

RefSeq Acc Id:

ENSP00000430941 ⟸ ENST00000524126

RefSeq Acc Id:	XP_047277594 ⟸ XM_047421638
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047277599 ⟸ XM_047421643
- Peptide Label:	isoform X11

RefSeq Acc Id:	XP_047277597 ⟸ XM_047421641
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_047277600 ⟸ XM_047421644
- Peptide Label:	isoform X13

RefSeq Acc Id:	XP_047277598 ⟸ XM_047421642
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_047277595 ⟸ XM_047421639
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047277596 ⟸ XM_047421640
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_047277601 ⟸ XM_047421645
- Peptide Label:	isoform X14

RefSeq Acc Id:	XP_047277606 ⟸ XM_047421650
- Peptide Label:	isoform X19

RefSeq Acc Id:	XP_047277604 ⟸ XM_047421648
- Peptide Label:	isoform X17

RefSeq Acc Id:	XP_047277605 ⟸ XM_047421649
- Peptide Label:	isoform X18

RefSeq Acc Id:	XP_047277603 ⟸ XM_047421647
- Peptide Label:	isoform X16

RefSeq Acc Id:	XP_047277602 ⟸ XM_047421646
- Peptide Label:	isoform X15

RefSeq Acc Id:	XP_047277607 ⟸ XM_047421651
- Peptide Label:	isoform X20

RefSeq Acc Id:	XP_047277608 ⟸ XM_047421652
- Peptide Label:	isoform X20

RefSeq Acc Id:	XP_054216177 ⟸ XM_054360202
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054216181 ⟸ XM_054360206
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054216178 ⟸ XM_054360203
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054216180 ⟸ XM_054360205
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054216187 ⟸ XM_054360212
- Peptide Label:	isoform X11

RefSeq Acc Id:	XP_054216185 ⟸ XM_054360210
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_054216188 ⟸ XM_054360213
- Peptide Label:	isoform X12

RefSeq Acc Id:	XP_054216179 ⟸ XM_054360204
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054216189 ⟸ XM_054360214
- Peptide Label:	isoform X13

RefSeq Acc Id:	XP_054216186 ⟸ XM_054360211
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_054216182 ⟸ XM_054360207
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054216183 ⟸ XM_054360208
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054216184 ⟸ XM_054360209
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_054216190 ⟸ XM_054360215
- Peptide Label:	isoform X14

RefSeq Acc Id:	XP_054216196 ⟸ XM_054360221
- Peptide Label:	isoform X19

RefSeq Acc Id:	XP_054216193 ⟸ XM_054360218
- Peptide Label:	isoform X17

RefSeq Acc Id:	XP_054216194 ⟸ XM_054360219
- Peptide Label:	isoform X18

RefSeq Acc Id:	XP_054216192 ⟸ XM_054360217
- Peptide Label:	isoform X16

RefSeq Acc Id:	XP_054216191 ⟸ XM_054360216
- Peptide Label:	isoform X15

RefSeq Acc Id:	XP_054216195 ⟸ XM_054360220
- Peptide Label:	isoform X20

RefSeq Acc Id:	XP_054216197 ⟸ XM_054360222
- Peptide Label:	isoform X20

RefSeq Acc Id:	XP_054216198 ⟸ XM_054360223
- Peptide Label:	isoform X20

Protein Domains

DUF4502 DUF4503

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q14159-F1-model_v2	AlphaFold	Q14159	1-915	view protein structure

Promoters

RGD ID:

7213251

Promoter ID:

EPDNEW_H12372

Type:

initiation region

Name:

SPIDR_2

Description:

scaffolding protein involved in DNA repair

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H12373

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,575 - 47,260,635	EPDNEW

RGD ID:

7213257

Promoter ID:

EPDNEW_H12373

Type:

initiation region

Name:

SPIDR_1

Description:

scaffolding protein involved in DNA repair

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H12372

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	47,260,938 - 47,260,998	EPDNEW

RGD ID:

6806819

Promoter ID:

HG_KWN:61247

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:

NM_001080394, UC003XQE.1, UC010LXS.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	48,335,654 - 48,336,154 (+)	MPROMDB

RGD ID:

6813429

Promoter ID:

HG_ACW:76990

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

KIAA0146.VDAPR07-UNSPLICED

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	48,810,226 - 48,810,726 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:28971	AgrOrtholog
COSMIC	SPIDR	COSMIC
Ensembl Genes	ENSG00000164808	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000297423	ENTREZGENE
	ENST00000297423.9	UniProtKB/Swiss-Prot
	ENST00000517619.5	UniProtKB/TrEMBL
	ENST00000517693	ENTREZGENE
	ENST00000517693.5	UniProtKB/TrEMBL
	ENST00000517824.5	UniProtKB/TrEMBL
	ENST00000518060.5	UniProtKB/TrEMBL
	ENST00000518074	ENTREZGENE
	ENST00000518074.5	UniProtKB/Swiss-Prot
	ENST00000519141	ENTREZGENE
	ENST00000519401	ENTREZGENE
	ENST00000519401.5	UniProtKB/TrEMBL
	ENST00000519661.5	UniProtKB/TrEMBL
	ENST00000521214	ENTREZGENE
	ENST00000522117	ENTREZGENE
	ENST00000522117.5	UniProtKB/TrEMBL
	ENST00000522222.5	UniProtKB/TrEMBL
	ENST00000523814.5	UniProtKB/TrEMBL
	ENST00000524006.5	UniProtKB/TrEMBL
	ENST00000524033.5	UniProtKB/TrEMBL
	ENST00000524126	ENTREZGENE
	ENST00000524126.5	UniProtKB/TrEMBL
	ENST00000541342	ENTREZGENE
	ENST00000541342.2	UniProtKB/Swiss-Prot
GTEx	ENSG00000164808	GTEx
HGNC ID	HGNC:28971	ENTREZGENE
Human Proteome Map	SPIDR	Human Proteome Map
InterPro	DUF4502	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DUF4503	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:23514	UniProtKB/Swiss-Prot
NCBI Gene	23514	ENTREZGENE
OMIM	615384	OMIM
PANTHER	DNA REPAIR-SCAFFOLDING PROTEIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DNA REPAIR-SCAFFOLDING PROTEIN SPIDR	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	DUF4502	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DUF4503	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA142671636	PharmGKB
UniProt	B3KP42	ENTREZGENE, UniProtKB/TrEMBL
	B4DEV5	ENTREZGENE, UniProtKB/TrEMBL
	B4DFV2	ENTREZGENE
	B4DMX9_HUMAN	UniProtKB/TrEMBL
	B4DWT8	ENTREZGENE, UniProtKB/TrEMBL
	B4DZY2	ENTREZGENE, UniProtKB/TrEMBL
	B4E0Y6	ENTREZGENE
	E5RFY2_HUMAN	UniProtKB/TrEMBL
	E5RGV8_HUMAN	UniProtKB/TrEMBL
	E5RGX8_HUMAN	UniProtKB/TrEMBL
	E5RHG3_HUMAN	UniProtKB/TrEMBL
	E5RIB8_HUMAN	UniProtKB/TrEMBL
	E5RIU7_HUMAN	UniProtKB/TrEMBL
	E5RJJ2_HUMAN	UniProtKB/TrEMBL
	E7EVI9_HUMAN	UniProtKB/TrEMBL
	H0YBC9	ENTREZGENE, UniProtKB/TrEMBL
	Q14159	ENTREZGENE
	Q96BI5	ENTREZGENE
	SPIDR_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	B4DFV2	UniProtKB/Swiss-Prot
	B4E0Y6	UniProtKB/Swiss-Prot
	Q96BI5	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2018-03-06	SPIDR	scaffold protein involved in DNA repair		scaffolding protein involved in DNA repair	Symbol and/or name change	5135510	APPROVED
2013-07-09	SPIDR	scaffolding protein involved in DNA repair	KIAA0146	KIAA0146	Symbol and/or name change	5135510	APPROVED

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

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

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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