C14orf93 (chromosome 14 open reading frame 93)

Gene: C14orf93 (chromosome 14 open reading frame 93) Homo sapiens

Analyze

Symbol:

C14orf93

Name:

chromosome 14 open reading frame 93

RGD ID:

1348927

HGNC Page

HGNC:20162

Description:

Enables RNA binding activity. Predicted to act upstream of or within cell differentiation and positive regulation of gene expression. Predicted to be located in extracellular region.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ12154; hypothetical protein LOC60686; regulator of thyroid function and cancer; RTFC; uncharacterized protein C14orf93

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	14	22,985,894 - 23,010,143 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	22,985,894 - 23,010,166 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	23,455,103 - 23,479,352 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	22,525,951 - 22,549,192 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	22,525,950 - 22,549,192	NCBI
Celera	14	3,319,000 - 3,342,250 (-)	NCBI		Celera
Cytogenetic Map	14	q11.2	NCBI
HuRef	14	3,573,344 - 3,596,639 (-)	NCBI		HuRef
CHM1_1	14	23,454,741 - 23,477,990 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	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

Brain-Lung-Thyroid Syndrome (IAGP)

genetic disease (IAGP)

lysinuric protein intolerance (IAGP)

Specific Granule Deficiency (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-schisandrin B (ISO)

17beta-estradiol (EXP)

2,2',4,4'-Tetrabromodiphenyl ether (ISO)

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

3-isobutyl-1-methyl-7H-xanthine (EXP)

acrylamide (ISO)

aflatoxin B1 (EXP)

benzo[a]pyrene (EXP)

bisphenol A (EXP,ISO)

cisplatin (EXP)

Cuprizon (ISO)

cyclosporin A (EXP)

dexamethasone (EXP)

dibutyl phthalate (ISO)

dorsomorphin (EXP)

FR900359 (EXP)

hydrogen peroxide (EXP)

indometacin (EXP)

methylmercury chloride (EXP)

nickel atom (EXP)

nitrofen (ISO)

paracetamol (EXP)

phenylmercury acetate (EXP)

resveratrol (EXP)

SB 431542 (EXP)

silicon dioxide (EXP)

sodium arsenite (EXP)

tetrachloromethane (ISO)

thioacetamide (ISO)

trichloroethene (ISO)

valproic acid (EXP)

vinclozolin (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

cell differentiation (IEA,ISO)

positive regulation of gene expression (IEA,ISO)

Cellular Component

extracellular region (IEA)

Molecular Function

protein binding (IPI)

RNA binding (HDA)

References

References - curated

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

Additional References at PubMed

PMID:12477932	PMID:14702039	PMID:15146197	PMID:15489334	PMID:16344560	PMID:18029348	PMID:21832049	PMID:22658674	PMID:22810586	PMID:23704328	PMID:25416956	PMID:26496610
PMID:26687479	PMID:27107014	PMID:27864143	PMID:28230092	PMID:30804502	PMID:33961781	PMID:35271311

Genomics

Comparative Map Data

C14orf93
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	22,985,894 - 23,010,166 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	23,455,103 - 23,479,352 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	22,525,951 - 22,549,192 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	22,525,950 - 22,549,192	NCBI
Celera	14	3,319,000 - 3,342,250 (-)	NCBI		Celera
Cytogenetic Map	14	q11.2	NCBI
HuRef	14	3,573,344 - 3,596,639 (-)	NCBI		HuRef
CHM1_1	14	23,454,741 - 23,477,990 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI		T2T-CHM13v2.0

4931414P19Rik
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	14	54,821,119 - 54,843,450 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	14	54,821,120 - 54,843,450 (-)	Ensembl		GRCm39 Ensembl
GRCm38	14	54,583,662 - 54,606,099 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	14	54,583,663 - 54,605,993 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	14	55,202,500 - 55,224,745 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	14	53,537,868 - 53,560,113 (-)	NCBI		MGSCv36	mm8
Celera	14	52,372,626 - 52,394,656 (-)	NCBI		Celera
Cytogenetic Map	14	C2	NCBI
cM Map	14	27.85	NCBI

C15h14orf93
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	15	32,007,591 - 32,034,337 (-)	NCBI		GRCr8
mRatBN7.2	15	28,037,567 - 28,064,347 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	15	28,037,574 - 28,064,274 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	15	29,876,988 - 29,903,676 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	15	31,024,204 - 31,050,889 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	15	29,273,748 - 29,300,352 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	15	33,225,172 - 33,250,609 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	15	33,224,896 - 33,250,546 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	15	37,109,226 - 37,143,944 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	15	32,656,277 - 32,688,050 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	15	27,616,290 - 27,642,915 (-)	NCBI		Celera
Cytogenetic Map	15	p13	NCBI

CUNH14orf93
(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_004955409	37,290,550 - 37,314,598 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955409	37,290,615 - 37,315,297 (+)	NCBI	ChiLan1.0	ChiLan1.0

C15H14orf93
(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	15	24,419,703 - 24,431,943 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	14	23,636,188 - 23,648,298 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	14	3,807,076 - 3,830,892 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	14	21,905,028 - 21,928,242 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	14	21,905,028 - 21,928,242 (-)	Ensembl	panpan1.1		panPan2

C8H14orf93
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	8	3,305,532 - 3,316,072 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	8	3,305,751 - 3,316,079 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	8	3,253,297 - 3,264,153 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	8	3,413,133 - 3,423,991 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	8	3,413,664 - 3,437,322 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	8	3,104,064 - 3,114,923 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	8	3,165,789 - 3,176,644 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	8	3,427,852 - 3,438,706 (-)	NCBI		UU_Cfam_GSD_1.0

CUNH14orf93
(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_024408640	35,060,954 - 35,084,717 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936722	1,316,789 - 1,328,059 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936722	1,304,357 - 1,327,726 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

C7H14orf93
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	7	76,045,686 - 76,058,891 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	7	76,033,750 - 76,061,877 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

CUNH14orf93
(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	29	23,356,885 - 23,381,273 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	29	23,355,798 - 23,369,839 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666059	23,038,445 - 23,063,808 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

CUNH14orf93
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624820	9,524,499 - 9,548,765 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624820	9,524,566 - 9,548,650 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in C14orf93
8 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 14q11.2(chr14:20151149-23442195)x3	copy number gain	See cases [RCV000050914]	Chr14:20151149..23442195 [GRCh38] Chr14:20619308..23911404 [GRCh37] Chr14:19689148..22981244 [NCBI36] Chr14:14q11.2	pathogenic
GRCh38/hg38 14q11.2-12(chr14:20151149-27723796)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051484]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051484]\|See cases [RCV000051484]	Chr14:20151149..27723796 [GRCh38] Chr14:20619308..28193002 [GRCh37] Chr14:19689148..27262842 [NCBI36] Chr14:14q11.2-12	pathogenic
GRCh38/hg38 14q11.2-21.2(chr14:20196945-45284802)x1	copy number loss	See cases [RCV000051485]	Chr14:20196945..45284802 [GRCh38] Chr14:20665104..45754005 [GRCh37] Chr14:19734944..44823755 [NCBI36] Chr14:14q11.2-21.2	pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:20000611-38984415)x3	copy number gain	See cases [RCV000053803]	Chr14:20000611..38984415 [GRCh38] Chr14:20468770..39453619 [GRCh37] Chr14:19538610..38523370 [NCBI36] Chr14:14q11.2-21.1	pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:20150949-39746154)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053806]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053806]\|See cases [RCV000053806]	Chr14:20150949..39746154 [GRCh38] Chr14:20619108..40215358 [GRCh37] Chr14:19688948..39285109 [NCBI36] Chr14:14q11.2-21.1	pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3	copy number gain	See cases [RCV000135543]	Chr14:20151149..106855263 [GRCh38] Chr14:20619308..107263478 [GRCh37] Chr14:19689148..106334523 [NCBI36] Chr14:14q11.2-32.33	pathogenic
GRCh38/hg38 14q11.2-12(chr14:20412587-25018120)x3	copy number gain	See cases [RCV000137725]	Chr14:20412587..25018120 [GRCh38] Chr14:20880746..25487326 [GRCh37] Chr14:19950586..24557166 [NCBI36] Chr14:14q11.2-12	likely pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3	copy number gain	See cases [RCV000143373]	Chr14:20043514..106877229 [GRCh38] Chr14:20511673..107285437 [GRCh37] Chr14:19581513..106356482 [NCBI36] Chr14:14q11.2-32.33	pathogenic
GRCh38/hg38 14q11.2-21.2(chr14:20022693-44093672)x3	copy number gain	See cases [RCV000143186]	Chr14:20022693..44093672 [GRCh38] Chr14:20490852..44562875 [GRCh37] Chr14:19560692..43632625 [NCBI36] Chr14:14q11.2-21.2	pathogenic
GRCh38/hg38 14q11.2-21.3(chr14:20043513-48642042)x3	copy number gain	See cases [RCV000143748]	Chr14:20043513..48642042 [GRCh38] Chr14:20511672..49111245 [GRCh37] Chr14:19581512..48180995 [NCBI36] Chr14:14q11.2-21.3	pathogenic
GRCh37/hg19 14q11.2-12(chr14:19100682-28730087)	copy number gain	not provided [RCV000767822]	Chr14:19100682..28730087 [GRCh37] Chr14:14q11.2-12	pathogenic
GRCh37/hg19 14q11.2-12(chr14:19794561-27768254)x3	copy number gain	See cases [RCV000240285]	Chr14:19794561..27768254 [GRCh37] Chr14:14q11.2-12	pathogenic
GRCh37/hg19 14q11.2-22.2(chr14:23164384-54733411)x3	copy number gain	See cases [RCV000447658]	Chr14:23164384..54733411 [GRCh37] Chr14:14q11.2-22.2	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3	copy number gain	See cases [RCV000446256]	Chr14:19794561..107234280 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2-13.1(chr14:19794561-34049214)x3	copy number gain	See cases [RCV000448273]	Chr14:19794561..34049214 [GRCh37] Chr14:14q11.2-13.1	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437)	copy number gain	See cases [RCV000512041]	Chr14:20511673..107285437 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2(chr14:23240787-23468899)x1	copy number loss	not provided [RCV000683591]	Chr14:23240787..23468899 [GRCh37] Chr14:14q11.2	uncertain significance
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3	copy number gain	not provided [RCV000738412]	Chr14:19000422..107289053 [GRCh37] Chr14:14q11.1-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3	copy number gain	not provided [RCV000738413]	Chr14:19280733..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3	copy number gain	not provided [RCV000738414]	Chr14:19327823..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2(chr14:21717093-24027220)x3	copy number gain	not provided [RCV000856644]	Chr14:21717093..24027220 [GRCh37] Chr14:14q11.2	likely pathogenic
NC_000014.8:g.(?_23242819)_(25103366_?)dup	duplication	Lysinuric protein intolerance [RCV003105428]\|Specific granule deficiency [RCV003105427]	Chr14:23242819..25103366 [GRCh37] Chr14:14q11.2-12	uncertain significance
NM_021944.4(C14orf93):c.105C>T (p.Ser35=)	single nucleotide variant	not provided [RCV000880444]	Chr14:22998919 [GRCh38] Chr14:23468128 [GRCh37] Chr14:14q11.2	benign
NM_021944.4(C14orf93):c.1329C>T (p.Arg443=)	single nucleotide variant	not provided [RCV000957197]	Chr14:22987503 [GRCh38] Chr14:23456712 [GRCh37] Chr14:14q11.2	benign
GRCh37/hg19 14q11.2-21.2(chr14:20511672-44829030)x3	copy number gain	not provided [RCV001006605]	Chr14:20511672..44829030 [GRCh37] Chr14:14q11.2-21.2	pathogenic
GRCh37/hg19 14q11.2-21.1(chr14:20511672-42881888)x3	copy number gain	not provided [RCV001249358]	Chr14:20511672..42881888 [GRCh37] Chr14:14q11.2-21.1	not provided
GRCh37/hg19 14q11.2(chr14:23457638-23698285)x3	copy number gain	not provided [RCV001259178]	Chr14:23457638..23698285 [GRCh37] Chr14:14q11.2	uncertain significance
GRCh37/hg19 14q11.2-21.3(chr14:20511672-47481203)	copy number gain	Seizure [RCV002280625]	Chr14:20511672..47481203 [GRCh37] Chr14:14q11.2-21.3	pathogenic
GRCh37/hg19 14q11.2(chr14:20925965-23649548)x3	copy number gain	14q11.2 microduplication [RCV001786536]	Chr14:20925965..23649548 [GRCh37] Chr14:14q11.2	likely pathogenic
NC_000014.8:g.(21162263_36986276)_(36987308_50713602)del	deletion	Brain-lung-thyroid syndrome [RCV002221171]	Chr14:36986276..36987308 [GRCh37] Chr14:14q11.2-21.3	pathogenic
NM_021944.4(C14orf93):c.145A>T (p.Thr49Ser)	single nucleotide variant	Inborn genetic diseases [RCV002772306]	Chr14:22998879 [GRCh38] Chr14:23468088 [GRCh37] Chr14:14q11.2	uncertain significance
NM_021944.4(C14orf93):c.1351C>T (p.Arg451Cys)	single nucleotide variant	Inborn genetic diseases [RCV002773092]	Chr14:22987481 [GRCh38] Chr14:23456690 [GRCh37] Chr14:14q11.2	uncertain significance
NM_021944.4(C14orf93):c.1507G>A (p.Glu503Lys)	single nucleotide variant	Inborn genetic diseases [RCV002926062]	Chr14:22987325 [GRCh38] Chr14:23456534 [GRCh37] Chr14:14q11.2	uncertain significance
NM_021944.4(C14orf93):c.854C>G (p.Ser285Cys)	single nucleotide variant	Inborn genetic diseases [RCV002762967]	Chr14:22996012 [GRCh38] Chr14:23465221 [GRCh37] Chr14:14q11.2	uncertain significance
GRCh37/hg19 14q11.2-23.1(chr14:20511673-61826023)x3	copy number gain	not provided [RCV003485022]	Chr14:20511673..61826023 [GRCh37] Chr14:14q11.2-23.1	pathogenic
NM_021944.4(C14orf93):c.533A>T (p.Gln178Leu)	single nucleotide variant	not provided [RCV003424942]	Chr14:22998491 [GRCh38] Chr14:23467700 [GRCh37] Chr14:14q11.2	likely benign

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	5919
Count of miRNA genes:	982
Interacting mature miRNAs:	1201
Transcripts:	ENST00000299088, ENST00000341470, ENST00000397376, ENST00000397377, ENST00000397379, ENST00000397380, ENST00000397382, ENST00000406429, ENST00000553316, ENST00000553606, ENST00000553675, ENST00000553931, ENST00000553958, ENST00000554179, ENST00000554536, ENST00000555098, ENST00000555575, ENST00000555998, ENST00000556419, ENST00000556812, ENST00000556896, ENST00000557513
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

SHGC-31862

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	23,456,423 - 23,456,552	UniSTS	GRCh37
Build 36	14	22,526,263 - 22,526,392	RGD	NCBI36
Celera	14	3,319,313 - 3,319,442	RGD
Cytogenetic Map	14	q11.2	UniSTS
HuRef	14	3,573,657 - 3,573,786	UniSTS
GeneMap99-G3 RH Map	14	392.0	UniSTS

G63676

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	23,464,449 - 23,464,550	UniSTS	GRCh37
Build 36	14	22,534,289 - 22,534,390	RGD	NCBI36
Celera	14	3,327,339 - 3,327,440	RGD
Cytogenetic Map	14	q11.2	UniSTS
HuRef	14	3,581,808 - 3,581,909	UniSTS
TNG Radiation Hybrid Map	14	984.0	UniSTS

AFMB073ZC5

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	23,465,981 - 23,466,256	UniSTS	GRCh37
Build 36	14	22,535,821 - 22,536,096	RGD	NCBI36
Celera	14	3,328,871 - 3,329,146	RGD
Cytogenetic Map	14	q11.2	UniSTS
HuRef	14	3,583,340 - 3,583,615	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

392

327

188

111

343

488

115

Low

2357

2860

1328

596

1617

436

4166

2145

3617

308

1117

1125

171

1190

2671

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001130706	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001130708	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001282968	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001282969	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001282970	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_021944	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005267971	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005267972	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006720231	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006720232	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011537059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011537060	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011537062	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021570	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021572	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021573	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021574	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021575	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021576	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449685	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449687	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431660	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431661	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431662	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431663	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431664	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431665	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431666	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431667	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431668	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431669	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431671	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431672	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376543	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376544	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376545	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376546	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376547	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376548	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376549	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376550	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376551	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AK022216	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK023026	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL132780	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AX880043	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC014299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC045740	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX161383	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX161417	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX161474	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX161507	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471078	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN309429	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA818572	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA891690	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000299088 ⟹ ENSP00000299088

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,985,894 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

ENST00000341470 ⟹ ENSP00000341353

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,986,902 - 23,010,132 (-)	Ensembl

RefSeq Acc Id:

ENST00000397376 ⟹ ENSP00000380532

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,995,948 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

ENST00000397377 ⟹ ENSP00000380533

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,987,145 - 23,010,122 (-)	Ensembl

RefSeq Acc Id:

ENST00000397379 ⟹ ENSP00000380535

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,987,123 - 23,010,128 (-)	Ensembl

RefSeq Acc Id:

ENST00000397380 ⟹ ENSP00000380536

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,996,240 - 23,002,769 (-)	Ensembl

RefSeq Acc Id:

ENST00000397382 ⟹ ENSP00000380538

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,987,129 - 23,010,166 (-)	Ensembl

RefSeq Acc Id:

ENST00000553316

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,999,103 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

ENST00000553606 ⟹ ENSP00000451155

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,996 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

ENST00000553675 ⟹ ENSP00000450771

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,427 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

ENST00000553931 ⟹ ENSP00000452036

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,615 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

ENST00000553958 ⟹ ENSP00000451456

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,773 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

ENST00000554179 ⟹ ENSP00000452088

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,996 - 23,010,151 (-)	Ensembl

RefSeq Acc Id:

ENST00000554536

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,621 - 23,010,133 (-)	Ensembl

RefSeq Acc Id:

ENST00000555098 ⟹ ENSP00000450866

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,788 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

ENST00000555575 ⟹ ENSP00000451111

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,705 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

ENST00000555998 ⟹ ENSP00000451879

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,875 - 23,010,133 (-)	Ensembl

RefSeq Acc Id:

ENST00000556419 ⟹ ENSP00000451762

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,991 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

ENST00000556812

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,998,721 - 23,010,096 (-)	Ensembl

RefSeq Acc Id:

ENST00000556896

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,999,121 - 23,007,123 (-)	Ensembl

RefSeq Acc Id:

ENST00000557513

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	22,999,045 - 23,010,143 (-)	Ensembl

RefSeq Acc Id:

NM_001130706 ⟹ NP_001124178

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI
GRCh37	14	23,456,110 - 23,479,375 (-)	NCBI
Celera	14	3,319,000 - 3,342,250 (-)	RGD
HuRef	14	3,573,344 - 3,596,689 (-)	NCBI
CHM1_1	14	23,454,741 - 23,478,040 (-)	NCBI
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

Sequence:

show sequence

CTTTTTGCACACACACGAATACAAAGAGCCATACGACCTTCGGTTTCAGGTTTAGCTGTGCCTC
CCAGTGACTATAATGACAAGGAAGCTGTAAATGTATTTGAGTTAAGCTTTTGCGAGAAACCCTA
CAGCTTGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTT
GATGCTTCCTACCTGTTGGAGCGGCCCAGCAGTGTAAGCGTGGTTGTTACTGCCCCATCCGCCA
TGTCCTTCAGTGCCACCATTCTCTTCTCCCCTCCCAGTGGCAGCGAGGCCAGATGCTGCTGCTG
CGCCTGTAAGAGTGAGACTAATGGAGGCAACACAGGCTCCCAGGGTGGGAATCCTCCTCCCAGC
ACCCCCATCACAGTGACTGGACATGGCTTGGCTGTTCAGAGCTCAGAGCAGCTCCTGCATGTTA
TCTACCAGCGGGTCGATAAGGCAGTGGGTTTGGCTGAAGCTGCTCTGGGTCTTGCCAGGGCCAA
CAATGAGTTGTTAAAACGTCTCCAGGAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTCCATC
CCTGATGAAGATGGGGAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTCAAGG
AAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGGGCAG
CGGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGGGCCT
TTGGGCTTCCCAGCAACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGCGAGG
CGGCCCCCCTGCTCAATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGTACAGCGAGT
TCTGGTCCCTGCTTATGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAGCGGGCAACC
CCAGAGACAGGACCAGAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACATGCTCAATG
CCGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGAGACA
CTCTCTAGGGCTGACCGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAGGCGC
AAGCGGGATCTTGTACTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCAATGACAAGA
GATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTCTGGA
AAAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTAAAAGGAGCC
TGTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAAGGCC
TGAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAACCGATCCAG
TATCATGAGGCATTTTGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAGGAACTGATG
TCAGATGAAGAGGACAGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTTCCGGG
CCCAGCGCCTCACAGAGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCACCAAAGCCAA
CCGTGTGTATGGGCCTCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACCAGAA
CTTTACAATCCTAATTTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACCTGGCTCCC
CATCTTTTGACCAACCCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAAATCAAGGT
GGAAAAGGATGAATAAAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCCATGTCTCA
GAAATAGGTGGCCATGGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGCAAAT
TTGCCTCTTTTCTTAACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAAAACTTATC
TAGAAGGGGAGAAACTCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCTCAGCATAA
ACAGTATCTCGGAGAAGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACATGAGGCCT
TCTTGACATATGCCCTGTCTCTGAGTTGTTTCTGCCCCTGCCCAGTTCCACCCAAAGCTCTGAG
GAAGCAGCCCAGGTTGTACCTTTTGCTTCCCTGTGACTACTTGTCTTGCTCTGCAGTGGAAACC
GAACATGACCAGTGCAGGTTAATACCGCCACCTGGTGGGCAGTTTCAGTCATGAGCTTGAGTCT
TCTGACCAAGGGAACACAAGTTCTATCACTATTGGGGAATTGGGTTCCTGATATAATAGCTATT
GTTTATTGAATTACATGAGGAAAATTTTACTATTCCTATCTTACAGATGAGGAAATTAAGGCTT
AAAGAGTTCCCGTGTCTCACCGGCAGCCTCTCTCTCACTATGTGACCAAGCAAAATACACAGCT
TTGTAGCTGTTTCTTGGTCCTGTCAGCCAAGCTGTATTTTGAGGAAGGGGTGTGCATTTTGGAT
GGATTGAAAAGCAAAAATGGCTTTACATTTATTCAGTCTTATAACAAACATTGATCGCTTTACT
AGGTGTCAGGTACTGTGCTATGGATACATTGTTGATAAGGTTGGATGCTGTTCAGAGATTTTTT
TAGTTTAGTCAGGAAGCCAGGCAGTGGAGTAGGCAATGAAATGAACTGTGATAAGGGTGACCAT
GGTGGAGTGTAGTGCACTATGGCAATATACAGCAGGGGTAGCTAACCTACTCTTGCAGTCTGGA
AAGGCTTCTTCTGAGAGGGTGTAATGTCTAAACTGGGGAAGAGTTAACCAGAAGGAAAGGGGAG
GCTAAGAGAGTGTTCCAAACAGGGAACTGCAGGTACAAAAGTCCAGGGGCAAGAGAGAGTACAG
ACAAGGTCCAGTTCTACTGCAGACTTTTGGGGAAGGGATAATGCTAGAGGAGAGGCTGGAGAGT
GAGACAGACCTCATAATACAGAGTACAGACTTCAACCCAAGGGCAGTGAGAAATCATTGAAAGT
TTGTTTTAGCAGGGAAATAAAACGACAGGTTTTGCCTACAGGCAGTCCCCAACTCAA

hide sequence

RefSeq Acc Id:

NM_001130708 ⟹ NP_001124180

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI
GRCh37	14	23,456,110 - 23,479,375 (-)	NCBI
Celera	14	3,319,000 - 3,342,250 (-)	RGD
HuRef	14	3,573,344 - 3,596,689 (-)	NCBI
CHM1_1	14	23,454,741 - 23,478,040 (-)	NCBI
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

Sequence:

show sequence

CTTTTTGCACACACACGAATACAAAGAGCCATACGACCTTCGGACCCTACAGCTTGGGGCCTGG
GCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTTGATGCTTCCTACCTG
TTGGAGCGGCCCAGCAGTGTAAGCGTGGTTGTTACTGCCCCATCCGCCATGTCCTTCAGTGCCA
CCATTCTCTTCTCCCCTCCCAGTGGCAGCGAGGCCAGATGCTGCTGCTGCGCCTGTAAGAGTGA
GACTAATGGAGGCAACACAGGCTCCCAGGGTGGGAATCCTCCTCCCAGCACCCCCATCACAGTG
ACTGGACATGGCTTGGCTGTTCAGAGCTCAGAGCAGCTCCTGCATGTTATCTACCAGCGGGTCG
ATAAGGCAGTGGGTTTGGCTGAAGCTGCTCTGGGTCTTGCCAGGGCCAACAATGAGTTGTTAAA
ACGTCTCCAGGAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTCCATCCCTGATGAAGATGGG
GAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGTCCCGGGGAAG
CCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGGGCAGCGGCGTGCAGGTGGT
GATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGGGCCTTTGGGCTTCCCAGCA
ACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGCGAGGCGGCCCCCCTGCTCA
ATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGTACAGCGAGTTCTGGTCCCTGCTTA
TGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAGCGGGCAACCCCAGAGACAGGACCA
GAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACATGCTCAATGCCGCTGCTGCGCTGG
ACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGAGACACTCTCTAGGGCTGAC
CGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAGGCGCAAGCGGGATCTTGTA
CTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCAATGACAAGAGATTCAATGGGTCTG
AAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTCTGGAAAAGCTCAAGCAAGA
GCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTAAAAGGAGCCTGTGTGGCCTACTTC
CTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAAGGCCTGAAGGAAAAAGAGG
AGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAACCGATCCAGTATCATGAGGCATTT
TGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAGGAACTGATGTCAGATGAAGAGGAC
AGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTTCCGGGCCCAGCGCCTCACAG
AGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCACCAAAGCCAACCGTGTGTATGGGCC
TCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACCAGAACTTTACAATCCTAAT
TTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACCTGGCTCCCCATCTTTTGACCAAC
CCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAAATCAAGGTGGAAAAGGATGAATA
AAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCCATGTCTCAGAAATAGGTGGCCAT
GGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGCAAATTTGCCTCTTTTCTTA
ACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAAAACTTATCTAGAAGGGGAGAAAC
TCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCTCAGCATAAACAGTATCTCGGAGA
AGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACATGAGGCCTTCTTGACATATGCCC
TGTCTCTGAGTTGTTTCTGCCCCTGCCCAGTTCCACCCAAAGCTCTGAGGAAGCAGCCCAGGTT
GTACCTTTTGCTTCCCTGTGACTACTTGTCTTGCTCTGCAGTGGAAACCGAACATGACCAGTGC
AGGTTAATACCGCCACCTGGTGGGCAGTTTCAGTCATGAGCTTGAGTCTTCTGACCAAGGGAAC
ACAAGTTCTATCACTATTGGGGAATTGGGTTCCTGATATAATAGCTATTGTTTATTGAATTACA
TGAGGAAAATTTTACTATTCCTATCTTACAGATGAGGAAATTAAGGCTTAAAGAGTTCCCGTGT
CTCACCGGCAGCCTCTCTCTCACTATGTGACCAAGCAAAATACACAGCTTTGTAGCTGTTTCTT
GGTCCTGTCAGCCAAGCTGTATTTTGAGGAAGGGGTGTGCATTTTGGATGGATTGAAAAGCAAA
AATGGCTTTACATTTATTCAGTCTTATAACAAACATTGATCGCTTTACTAGGTGTCAGGTACTG
TGCTATGGATACATTGTTGATAAGGTTGGATGCTGTTCAGAGATTTTTTTAGTTTAGTCAGGAA
GCCAGGCAGTGGAGTAGGCAATGAAATGAACTGTGATAAGGGTGACCATGGTGGAGTGTAGTGC
ACTATGGCAATATACAGCAGGGGTAGCTAACCTACTCTTGCAGTCTGGAAAGGCTTCTTCTGAG
AGGGTGTAATGTCTAAACTGGGGAAGAGTTAACCAGAAGGAAAGGGGAGGCTAAGAGAGTGTTC
CAAACAGGGAACTGCAGGTACAAAAGTCCAGGGGCAAGAGAGAGTACAGACAAGGTCCAGTTCT
ACTGCAGACTTTTGGGGAAGGGATAATGCTAGAGGAGAGGCTGGAGAGTGAGACAGACCTCATA
ATACAGAGTACAGACTTCAACCCAAGGGCAGTGAGAAATCATTGAAAGTTTGTTTTAGCAGGGA
AATAAAACGACAGGTTTTGCCTACAGGCAGTCCCCAACTCAA

hide sequence

RefSeq Acc Id:

NM_001282968 ⟹ NP_001269897

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI
HuRef	14	3,573,344 - 3,596,689 (-)	NCBI
CHM1_1	14	23,454,741 - 23,478,040 (-)	NCBI
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

Sequence:

show sequence

CTTTTTGCACACACACGAATACAAAGAGCCATACGACCTTCGGATGCCGGAAGGTCCTTCTGAA
TCCCTTCCCTGTTCCTTAGGTTGCACTAGTCGGGGGTTCCATGCTGGGGGGCAGAAGGAATGCT
CTCTACCGTCTGAAACCGTTCATCAGGAAGGCCTTGATTTGTGATGTGCTAGGAGAGCACAGGA
TCTGCAAATAGAAGGCACCTGTCTCCCTTCTGCAGGCCGAGGAGAGGCCGCCATGGACTGTGTG
CTTCTTCATGGCTTGTTTACTCTTCTTTCACAGACCCTACAGCTTGGGGCCTGGGCTCCTCTGA
CCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTTGATGCTTCCTACCTGTTGGAGCGGC
CCAGCAGTGAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTCCATCCCTGATGAAGATGGGGA
AAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGTCCCGGGGAAGCC
TTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGGGCAGCGGCGTGCAGGTGGTGA
TTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGGGCCTTTGGGCTTCCCAGCAAC
TCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGCGAGGCGGCCCCCCTGCTCAAT
CCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGTACAGCGAGTTCTGGTCCCTGCTTATG
CCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAGCGGGCAACCCCAGAGACAGGACCAGA
AAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACATGCTCAATGCCGCTGCTGCGCTGGAC
AGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGAGACACTCTCTAGGGCTGACCG
TTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAGGCGCAAGCGGGATCTTGTACT
CTCTAAACTGGTCCACAATGTGCATAACCACATCACCAATGACAAGAGATTCAATGGGTCTGAA
AGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTCTGGAAAAGCTCAAGCAAGAGC
TGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTAAAAGGAGCCTGTGTGGCCTACTTCCT
TACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAAGGCCTGAAGGAAAAAGAGGAG
AAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAACCGATCCAGTATCATGAGGCATTTTG
GACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAGGAACTGATGTCAGATGAAGAGGACAG
TCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTTCCGGGCCCAGCGCCTCACAGAG
CTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCACCAAAGCCAACCGTGTGTATGGGCCTC
CCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACCAGAACTTTACAATCCTAATTT
CCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACCTGGCTCCCCATCTTTTGACCAACCC
CACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAAATCAAGGTGGAAAAGGATGAATAAA
ATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCCATGTCTCAGAAATAGGTGGCCATGG
GGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGCAAATTTGCCTCTTTTCTTAAC
ACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAAAACTTATCTAGAAGGGGAGAAACTC
CCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCTCAGCATAAACAGTATCTCGGAGAAG
CCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACATGAGGCCTTCTTGACATATGCCCTG
TCTCTGAGTTGTTTCTGCCCCTGCCCAGTTCCACCCAAAGCTCTGAGGAAGCAGCCCAGGTTGT
ACCTTTTGCTTCCCTGTGACTACTTGTCTTGCTCTGCAGTGGAAACCGAACATGACCAGTGCAG
GTTAATACCGCCACCTGGTGGGCAGTTTCAGTCATGAGCTTGAGTCTTCTGACCAAGGGAACAC
AAGTTCTATCACTATTGGGGAATTGGGTTCCTGATATAATAGCTATTGTTTATTGAATTACATG
AGGAAAATTTTACTATTCCTATCTTACAGATGAGGAAATTAAGGCTTAAAGAGTTCCCGTGTCT
CACCGGCAGCCTCTCTCTCACTATGTGACCAAGCAAAATACACAGCTTTGTAGCTGTTTCTTGG
TCCTGTCAGCCAAGCTGTATTTTGAGGAAGGGGTGTGCATTTTGGATGGATTGAAAAGCAAAAA
TGGCTTTACATTTATTCAGTCTTATAACAAACATTGATCGCTTTACTAGGTGTCAGGTACTGTG
CTATGGATACATTGTTGATAAGGTTGGATGCTGTTCAGAGATTTTTTTAGTTTAGTCAGGAAGC
CAGGCAGTGGAGTAGGCAATGAAATGAACTGTGATAAGGGTGACCATGGTGGAGTGTAGTGCAC
TATGGCAATATACAGCAGGGGTAGCTAACCTACTCTTGCAGTCTGGAAAGGCTTCTTCTGAGAG
GGTGTAATGTCTAAACTGGGGAAGAGTTAACCAGAAGGAAAGGGGAGGCTAAGAGAGTGTTCCA
AACAGGGAACTGCAGGTACAAAAGTCCAGGGGCAAGAGAGAGTACAGACAAGGTCCAGTTCTAC
TGCAGACTTTTGGGGAAGGGATAATGCTAGAGGAGAGGCTGGAGAGTGAGACAGACCTCATAAT
ACAGAGTACAGACTTCAACCCAAGGGCAGTGAGAAATCATTGAAAGTTTGTTTTAGCAGGGAAA
TAAAACGACAGGTTTTGCCTACAGGCAGTCCCCAACTCAA

hide sequence

RefSeq Acc Id:

NM_001282969 ⟹ NP_001269898

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,986,901 - 23,001,037 (-)	NCBI
HuRef	14	3,573,344 - 3,596,689 (-)	NCBI
CHM1_1	14	23,454,741 - 23,468,864 (-)	NCBI
T2T-CHM13v2.0	14	17,187,519 - 17,201,655 (-)	NCBI

Sequence:

show sequence

TTTCAGGTTTAGCTGTGCCTCCCAGTGACTATAATGACAAGGAAGCTGTAAATGTATTTGAGTT
AAGCTTTTGCGAGAAACCCTACAGCTTGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAG
GAAAGTGAGTCCAGAGAAGTTGATGCTTCCTACCTGTTGGAGCGGCCCAGCAGTGAGGAAGTGG
GTGACCTGAGGCAAGGGAAAGTGTCCATCCCTGATGAAGATGGGGAAAGCCGGGCACATAGTTC
CCCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCC
GTGGAAGAGGAGTGTGACAGCGTGGGCAGCGGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGC
TGGGAGCAGCCTCAGTGGGGCCTGGGCCTTTGGGCTTCCCAGCAACTCAGAGGGACATGCGGCT
CCCAGGGTGCACGCTGGCTGCCAGCGAGGCGGCCCCCCTGCTCAATCCTCTGGTGGATGATTAC
GTGGCCTCTGAGGGTGCAGTACAGCGAGTTCTGGTCCCTGCTTATGCCAAGCAACTCTCACCAG
CCACACAACTGGCAATCCAGCGGGCAACCCCAGAGACAGGACCAGAAAATGGAACCAAGCTGCC
ACCACCCCGCCCTGAGGACATGCTCAATGCCGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCA
GGCCCTGGGAGCACTGGGGAGCTGAGACACTCTCTAGGGCTGACCGTTTCCCCATGCAGGACCA
GAGGAAGTGGGCAGAAGAACTCCAGGCGCAAGCGGGATCTTGTACTCTCTAAACTGGTCCACAA
TGTGCATAACCACATCACCAATGACAAGAGATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGG
AATATTTCAGTAGTGAAGTTTCTTCTGGAAAAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACA
ATTACACTGATAAGGAGCTAAAAGGAGCCTGTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTA
CCGCAACTCCCTGAACCCCTTTAAAGGCCTGAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGC
CGATATCGGCTTTTTGCCAACCGATCCAGTATCATGAGGCATTTTGGACCTGAGGACCAACGTC
TGTGGAATGATGTGACAGAGGAACTGATGTCAGATGAAGAGGACAGTCTTAACGAGCCAGGTGT
GTGGGTGGCCCGCCCTCCCCGTTTCCGGGCCCAGCGCCTCACAGAGCTCTGCTACCACCTGGAT
GCTAACTCTAAGCATGGCACCAAAGCCAACCGTGTGTATGGGCCTCCCTCAGACAGACTGCCTT
CTGCTGAAGCCCAGCTCCTTCCACCAGAACTTTACAATCCTAATTTCCAAGAAGAGGAAGATGA
GGGAGGGGATGAGAATGCACCTGGCTCCCCATCTTTTGACCAACCCCACAAAACCTGCTGTCCT
GACTTGAACTCATTCATTGAAATCAAGGTGGAAAAGGATGAATAAAATCTACAGCCAAGAATAA
CTCTGGCTTCCGCCATGCCCCATGTCTCAGAAATAGGTGGCCATGGGGCTTCACAAAATAATGA
GATGCTCTGTGCAGTCTGAGAAAGCAAATTTGCCTCTTTTCTTAACACAGTCTCTACTGGGGAA
GCAGAACACTGGTGGGATAAAAACTTATCTAGAAGGGGAGAAACTCCCTCCACTGTGAACAGTA
AGCCAGAATATGCTTATTCCTCAGCATAAACAGTATCTCGGAGAAGCCTGGGATGAGAAAATGA
GGAGGATGGGTCCAAGAAACATGAGGCCTTCTTGACATAAAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_001282970 ⟹ NP_001269899

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,986,901 - 23,010,143 (-)	NCBI
HuRef	14	3,573,344 - 3,596,689 (-)	NCBI
CHM1_1	14	23,454,741 - 23,478,040 (-)	NCBI
T2T-CHM13v2.0	14	17,187,519 - 17,210,763 (-)	NCBI

Sequence:

show sequence

CTTTTTGCACACACACGAATACAAAGAGCCATACGACCTTCGGATGCCGGAAGGTCCTTCTGAA
TCCCTTCCCTGTTCCTTAGGTTGCACTAGTCGGGGGTTCCATGCTGGGGGGCAGAAGGAATGCT
CTCTACCGTCTGAAACCGTTCATCAGGAAGGCCTTGATTTGTGATGTGCTAGGAGAGCACAGGA
TCTGCAAATAGAAGGCACCTGTCTCCCTTCTGCAGGCCGAGGAGAGGCCGCCATGGACTGTGTG
CTTCTTCATGGCTTGTTTACTCTTCTTTCACAGACCCTACAGCTTGGGGCCTGGGCTCCTCTGA
CCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTTGATGCTTCCTACCTGTTGGAGCGGC
CCAGCAGTGTAAGCGTGGTTGTTACTGCCCCATCCGCCATGTCCTTCAGTGCCACCATTCTCTT
CTCCCCTCCCAGTGGCAGCGAGGCCAGATGCTGCTGCTGCGCCTGTAAGAGTGAGACTAATGGA
GGCAACACAGGCTCCCAGGGTGGGAATCCTCCTCCCAGCACCCCCATCACAGTGACTGGACATG
GCTTGGCTGTTCAGAGCTCAGAGCAGCTCCTGCATGTTATCTACCAGCGGGTCGATAAGGCAGT
GGGTTTGGCTGAAGCTGCTCTGGGTCTTGCCAGGGCCAACAATGAGTTGTTAAAACGTCTCCAG
GAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTCCATCCCTGATGAAGATGGGGAAAGCCGGG
CACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGGC
TCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGGGCAGCGGCGTGCAGGTGGTGATTGAGGAG
CTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGGGCCTTTGGGCTTCCCAGCAACTCAGAGGG
ACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGCGAGGCGGCCCCCCTGCTCAATCCTCTGGT
GGATGATTACGTGGCCTCTGAGGGTGCAGTACAGCGAGTTCTGGTCCCTGCTTATGCCAAGCAA
CTCTCACCAGCCACACAACTGGCAATCCAGCGGGCAACCCCAGAGACAGGACCAGAAAATGGAA
CCAAGCTGCCACCACCCCGCCCTGAGGACATGCTCAATGCCGCTGCTGCGCTGGACAGTGCCTT
GGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGAGACACTCTCTAGGGCTGACCGTTTCCCCA
TGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAGGCGCAAGCGGGATCTTGTACTCTCTAAAC
TGGTCCACAATGTGCATAACCACATCACCAATGACAAGAGATTCAATGGGTCTGAAAGCATCAA
GTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTCTGGAAAAGCTCAAGCAAGAGCTGGTGACC
AGTCCCCACAATTACACTGATAAGGAGCTAAAAGGAGCCTGTGTGGCCTACTTCCTTACTAAGA
GGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAAGGCCTGAAGGAAAAAGAGGAGAAGAAACT
TCGAAGTCGCCGATATCGGCTTTTTGCCAACCGATCCAGTATCATGAGGCATTTTGGACCTGAG
GACCAACGTCTGTGGAATGATGTGACAGAGGAACTGATGTCAGATGAAGAGGACAGTCTTAACG
AGCCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACCAGAACTTTACAATCCTAATTT
CCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACCTGGCTCCCCATCTTTTGACCAACCC
CACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAAATCAAGGTGGAAAAGGATGAATAAA
ATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCCATGTCTCAGAAATAGGTGGCCATGG
GGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGCAAATTTGCCTCTTTTCTTAAC
ACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAAAACTTATCTAGAAGGGGAGAAACTC
CCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCTCAGCATAAACAGTATCTCGGAGAAG
CCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACATGAGGCCTTCTTGACATA

hide sequence

RefSeq Acc Id:

NM_021944 ⟹ NP_068763

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI
GRCh37	14	23,456,110 - 23,479,375 (-)	NCBI
Build 36	14	22,525,951 - 22,549,192 (-)	NCBI Archive
Celera	14	3,319,000 - 3,342,250 (-)	RGD
HuRef	14	3,573,344 - 3,596,689 (-)	NCBI
CHM1_1	14	23,454,741 - 23,478,040 (-)	NCBI
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

Sequence:

show sequence

CTTTTTGCACACACACGAATACAAAGAGCCATACGACCTTCGGATGCCGGAAGGTCCTTCTGAA
TCCCTTCCCTGTTCCTTAGGTTGCACTAGTCGGGGGTTCCATGCTGGGGGGCAGAAGGAATGCT
CTCTACCGTCTGAAACCGTTCATCAGGAAGGCCTTGATTTGTGATGTGCTAGGAGAGCACAGGA
TCTGCAAATAGAAGGCACCTGTCTCCCTTCTGCAGGCCGAGGAGAGGCCGCCATGGACTGTGTG
CTTCTTCATGGCTTGTTTACTCTTCTTTCACAGACCCTACAGCTTGGGGCCTGGGCTCCTCTGA
CCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTTGATGCTTCCTACCTGTTGGAGCGGC
CCAGCAGTGTAAGCGTGGTTGTTACTGCCCCATCCGCCATGTCCTTCAGTGCCACCATTCTCTT
CTCCCCTCCCAGTGGCAGCGAGGCCAGATGCTGCTGCTGCGCCTGTAAGAGTGAGACTAATGGA
GGCAACACAGGCTCCCAGGGTGGGAATCCTCCTCCCAGCACCCCCATCACAGTGACTGGACATG
GCTTGGCTGTTCAGAGCTCAGAGCAGCTCCTGCATGTTATCTACCAGCGGGTCGATAAGGCAGT
GGGTTTGGCTGAAGCTGCTCTGGGTCTTGCCAGGGCCAACAATGAGTTGTTAAAACGTCTCCAG
GAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTCCATCCCTGATGAAGATGGGGAAAGCCGGG
CACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGGC
TCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGGGCAGCGGCGTGCAGGTGGTGATTGAGGAG
CTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGGGCCTTTGGGCTTCCCAGCAACTCAGAGGG
ACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGCGAGGCGGCCCCCCTGCTCAATCCTCTGGT
GGATGATTACGTGGCCTCTGAGGGTGCAGTACAGCGAGTTCTGGTCCCTGCTTATGCCAAGCAA
CTCTCACCAGCCACACAACTGGCAATCCAGCGGGCAACCCCAGAGACAGGACCAGAAAATGGAA
CCAAGCTGCCACCACCCCGCCCTGAGGACATGCTCAATGCCGCTGCTGCGCTGGACAGTGCCTT
GGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGAGACACTCTCTAGGGCTGACCGTTTCCCCA
TGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAGGCGCAAGCGGGATCTTGTACTCTCTAAAC
TGGTCCACAATGTGCATAACCACATCACCAATGACAAGAGATTCAATGGGTCTGAAAGCATCAA
GTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTCTGGAAAAGCTCAAGCAAGAGCTGGTGACC
AGTCCCCACAATTACACTGATAAGGAGCTAAAAGGAGCCTGTGTGGCCTACTTCCTTACTAAGA
GGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAAGGCCTGAAGGAAAAAGAGGAGAAGAAACT
TCGAAGTCGCCGATATCGGCTTTTTGCCAACCGATCCAGTATCATGAGGCATTTTGGACCTGAG
GACCAACGTCTGTGGAATGATGTGACAGAGGAACTGATGTCAGATGAAGAGGACAGTCTTAACG
AGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTTCCGGGCCCAGCGCCTCACAGAGCTCTGCTA
CCACCTGGATGCTAACTCTAAGCATGGCACCAAAGCCAACCGTGTGTATGGGCCTCCCTCAGAC
AGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACCAGAACTTTACAATCCTAATTTCCAAGAAG
AGGAAGATGAGGGAGGGGATGAGAATGCACCTGGCTCCCCATCTTTTGACCAACCCCACAAAAC
CTGCTGTCCTGACTTGAACTCATTCATTGAAATCAAGGTGGAAAAGGATGAATAAAATCTACAG
CCAAGAATAACTCTGGCTTCCGCCATGCCCCATGTCTCAGAAATAGGTGGCCATGGGGCTTCAC
AAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGCAAATTTGCCTCTTTTCTTAACACAGTCTC
TACTGGGGAAGCAGAACACTGGTGGGATAAAAACTTATCTAGAAGGGGAGAAACTCCCTCCACT
GTGAACAGTAAGCCAGAATATGCTTATTCCTCAGCATAAACAGTATCTCGGAGAAGCCTGGGAT
GAGAAAATGAGGAGGATGGGTCCAAGAAACATGAGGCCTTCTTGACATATGCCCTGTCTCTGAG
TTGTTTCTGCCCCTGCCCAGTTCCACCCAAAGCTCTGAGGAAGCAGCCCAGGTTGTACCTTTTG
CTTCCCTGTGACTACTTGTCTTGCTCTGCAGTGGAAACCGAACATGACCAGTGCAGGTTAATAC
CGCCACCTGGTGGGCAGTTTCAGTCATGAGCTTGAGTCTTCTGACCAAGGGAACACAAGTTCTA
TCACTATTGGGGAATTGGGTTCCTGATATAATAGCTATTGTTTATTGAATTACATGAGGAAAAT
TTTACTATTCCTATCTTACAGATGAGGAAATTAAGGCTTAAAGAGTTCCCGTGTCTCACCGGCA
GCCTCTCTCTCACTATGTGACCAAGCAAAATACACAGCTTTGTAGCTGTTTCTTGGTCCTGTCA
GCCAAGCTGTATTTTGAGGAAGGGGTGTGCATTTTGGATGGATTGAAAAGCAAAAATGGCTTTA
CATTTATTCAGTCTTATAACAAACATTGATCGCTTTACTAGGTGTCAGGTACTGTGCTATGGAT
ACATTGTTGATAAGGTTGGATGCTGTTCAGAGATTTTTTTAGTTTAGTCAGGAAGCCAGGCAGT
GGAGTAGGCAATGAAATGAACTGTGATAAGGGTGACCATGGTGGAGTGTAGTGCACTATGGCAA
TATACAGCAGGGGTAGCTAACCTACTCTTGCAGTCTGGAAAGGCTTCTTCTGAGAGGGTGTAAT
GTCTAAACTGGGGAAGAGTTAACCAGAAGGAAAGGGGAGGCTAAGAGAGTGTTCCAAACAGGGA
ACTGCAGGTACAAAAGTCCAGGGGCAAGAGAGAGTACAGACAAGGTCCAGTTCTACTGCAGACT
TTTGGGGAAGGGATAATGCTAGAGGAGAGGCTGGAGAGTGAGACAGACCTCATAATACAGAGTA
CAGACTTCAACCCAAGGGCAGTGAGAAATCATTGAAAGTTTGTTTTAGCAGGGAAATAAAACGA
CAGGTTTTGCCTACAGGCAGTCCCCAACTCAA

hide sequence

RefSeq Acc Id:

XM_005267971 ⟹ XP_005268028

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

CTTTTTGCACACACACGAATACAAAGAGCCATACGACCTTCGGGTTGCACTAGTCGGGGGTTCC
ATGCTGGGGGGCAGAAGGAATGCTCTCTACCGTCTGAAACCGTTCATCAGGAAGGCCTTGATTT
GTGATGTGCTAGGAGAGCACAGGATCTGCAAATAGAAGGCACCTGTCTCCCTTCTGCAGGCCGA
GGAGAGGCCGCCATGGACTGTGTGCTTCTTCATGGCTTGTTTACTCTTCTTTCACAGACCCTAC
AGCTTGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTTG
ATGCTTCCTACCTGTTGGAGCGGCCCAGCAGTGTAAGCGTGGTTGTTACTGCCCCATCCGCCAT
GTCCTTCAGTGCCACCATTCTCTTCTCCCCTCCCAGTGGCAGCGAGGCCAGATGCTGCTGCTGC
GCCTGTAAGAGTGAGACTAATGGAGGCAACACAGGCTCCCAGGGTGGGAATCCTCCTCCCAGCA
CCCCCATCACAGTGACTGGACATGGCTTGGCTGTTCAGAGCTCAGAGCAGCTCCTGCATGTTAT
CTACCAGCGGGTCGATAAGGCAGTGGGTTTGGCTGAAGCTGCTCTGGGTCTTGCCAGGGCCAAC
AATGAGTTGTTAAAACGTCTCCAGGAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTCCATCC
CTGATGAAGATGGGGAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTCAAGGA
AAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGGGCAGC
GGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGGGCCTT
TGGGCTTCCCAGCAACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGCGAGGC
GGCCCCCCTGCTCAATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGTACAGCGAGTT
CTGGTCCCTGCTTATGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAGCGGGCAACCC
CAGAGACAGGACCAGAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACATGCTCAATGC
CGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGAGACAC
TCTCTAGGGCTGACCGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAGGCGCA
AGCGGGATCTTGTACTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCAATGACAAGAG
ATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTCTGGAA
AAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTAAAAGGAGCCT
GTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAAGGCCT
GAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAACCGATCCAGT
ATCATGAGGCATTTTGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAGGAACTGATGT
CAGATGAAGAGGACAGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTTCCGGGC
CCAGCGCCTCACAGAGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCACCAAAGCCAAC
CGTGTGTATGGGCCTCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACCAGAAC
TTTACAATCCTAATTTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACCTGGCTCCCC
ATCTTTTGACCAACCCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAAATCAAGGTG
GAAAAGGATGAATAAAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCCATGTCTCAG
AAATAGGTGGCCATGGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGCAAATT
TGCCTCTTTTCTTAACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAAAACTTATCT
AGAAGGGGAGAAACTCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCTCAGCATAAA
CAGTATCTCGGAGAAGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACATGAGGCCTT
CTTGACA

hide sequence

RefSeq Acc Id:

XM_005267972 ⟹ XP_005268029

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

CTTTTTGCACACACACGAATACAAAGAGCCATACGACCTTCGGGTATCCTTTTTCCATTTTTTT
TCCTCCTTAATCTTGTGTGTGTTTTCAAATTTTTTAAAAATAGAGATCTGTAGCAGTGTTGGGA
CCCTACAGCTTGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAG
AAGTTGATGCTTCCTACCTGTTGGAGCGGCCCAGCAGTGTAAGCGTGGTTGTTACTGCCCCATC
CGCCATGTCCTTCAGTGCCACCATTCTCTTCTCCCCTCCCAGTGGCAGCGAGGCCAGATGCTGC
TGCTGCGCCTGTAAGAGTGAGACTAATGGAGGCAACACAGGCTCCCAGGGTGGGAATCCTCCTC
CCAGCACCCCCATCACAGTGACTGGACATGGCTTGGCTGTTCAGAGCTCAGAGCAGCTCCTGCA
TGTTATCTACCAGCGGGTCGATAAGGCAGTGGGTTTGGCTGAAGCTGCTCTGGGTCTTGCCAGG
GCCAACAATGAGTTGTTAAAACGTCTCCAGGAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGT
CCATCCCTGATGAAGATGGGGAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGCCTCT
CAAGGAAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTG
GGCAGCGGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTG
GGCCTTTGGGCTTCCCAGCAACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAG
CGAGGCGGCCCCCCTGCTCAATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGTACAG
CGAGTTCTGGTCCCTGCTTATGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAGCGGG
CAACCCCAGAGACAGGACCAGAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACATGCT
CAATGCCGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTG
AGACACTCTCTAGGGCTGACCGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCA
GGCGCAAGCGGGATCTTGTACTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCAATGA
CAAGAGATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTT
CTGGAAAAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTAAAAG
GAGCCTGTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCTTTAA
AGGCCTGAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAACCGA
TCCAGTATCATGAGGCATTTTGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAGGAAC
TGATGTCAGATGAAGAGGACAGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTT
CCGGGCCCAGCGCCTCACAGAGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCACCAAA
GCCAACCGTGTGTATGGGCCTCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCAC
CAGAACTTTACAATCCTAATTTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACCTGG
CTCCCCATCTTTTGACCAACCCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAAATC
AAGGTGGAAAAGGATGAATAAAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCCATG
TCTCAGAAATAGGTGGCCATGGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAG
CAAATTTGCCTCTTTTCTTAACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAAAAC
TTATCTAGAAGGGGAGAAACTCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCTCAG
CATAAACAGTATCTCGGAGAAGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACATGA
GGCCTTCTTGACA

hide sequence

RefSeq Acc Id:

XM_006720231 ⟹ XP_006720294

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

CTTTTTGCACACACACGAATACAAAGAGCCATACGACCTTCGGGTATCCTTTTTCCATTTTTTT
TCCTCCTTAATCTTGTGTGTGTTTTCAAATTTTTTAAAAATAGAGATCTGTAGCAGTGTTGGGA
CCCTACAGCTTGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAG
AAGTTGATGCTTCCTACCTGTTGGAGCGGCCCAGCAGTGAGGAAGTGGGTGACCTGAGGCAAGG
GAAAGTGTCCATCCCTGATGAAGATGGGGAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCT
GGGCCTCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTG
ACAGCGTGGGCAGCGGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGT
GGGGCCTGGGCCTTTGGGCTTCCCAGCAACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTG
GCTGCCAGCGAGGCGGCCCCCCTGCTCAATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTG
CAGTACAGCGAGTTCTGGTCCCTGCTTATGCCAAGCAACTCTCACCAGCCACACAACTGGCAAT
CCAGCGGGCAACCCCAGAGACAGGACCAGAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAG
GACATGCTCAATGCCGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTG
GGGAGCTGAGACACTCTCTAGGGCTGACCGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAA
GAACTCCAGGCGCAAGCGGGATCTTGTACTCTCTAAACTGGTCCACAATGTGCATAACCACATC
ACCAATGACAAGAGATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGA
AGTTTCTTCTGGAAAAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACAATTACACTGATAAGGA
GCTAAAAGGAGCCTGTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAAC
CCCTTTAAAGGCCTGAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTG
CCAACCGATCCAGTATCATGAGGCATTTTGGACCTGAGGACCAACGTCTGTGGAATGATGTGAC
AGAGGAACTGATGTCAGATGAAGAGGACAGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCT
CCCCGTTTCCGGGCCCAGCGCCTCACAGAGCTCTGCTACCACCTGGATGCTAACTCTAAGCATG
GCACCAAAGCCAACCGTGTGTATGGGCCTCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCT
CCTTCCACCAGAACTTTACAATCCTAATTTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAAT
GCACCTGGCTCCCCATCTTTTGACCAACCCCACAAAACCTGCTGTCCTGACTTGAACTCATTCA
TTGAAATCAAGGTGGAAAAGGATGAATAAAATCTACAGCCAAGAATAACTCTGGCTTCCGCCAT
GCCCCATGTCTCAGAAATAGGTGGCCATGGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTC
TGAGAAAGCAAATTTGCCTCTTTTCTTAACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGG
ATAAAAACTTATCTAGAAGGGGAGAAACTCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTA
TTCCTCAGCATAAACAGTATCTCGGAGAAGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAG
AAACATGAGGCCTTCTTGACA

hide sequence

RefSeq Acc Id:

XM_006720232 ⟹ XP_006720295

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

CTTTTTGCACACACACGAATACAAAGAGCCATACGACCTTCGGTTTCAGGTTTAGCTGTGCCTC
CCAGTGACTATAATGACAAGGAAGCTGTAAATGTATTTGAGTTAAGCTTTTGCGAGAAACCCTA
CAGCTTGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTT
GATGCTTCCTACCTGTTGGAGCGGCCCAGCAGTGAGGAAGTGGGTGACCTGAGGCAAGGGAAAG
TGTCCATCCCTGATGAAGATGGGGAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGCC
TCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAGC
GTGGGCAGCGGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGC
CTGGGCCTTTGGGCTTCCCAGCAACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTGC
CAGCGAGGCGGCCCCCCTGCTCAATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGTA
CAGCGAGTTCTGGTCCCTGCTTATGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAGC
GGGCAACCCCAGAGACAGGACCAGAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACAT
GCTCAATGCCGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGAG
CTGAGACACTCTCTAGGGCTGACCGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAACT
CCAGGCGCAAGCGGGATCTTGTACTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCAA
TGACAAGAGATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTTT
CTTCTGGAAAAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTAA
AAGGAGCCTGTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCTT
TAAAGGCCTGAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAAC
CGATCCAGTATCATGAGGCATTTTGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAGG
AACTGATGTCAGATGAAGAGGACAGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCG
TTTCCGGGCCCAGCGCCTCACAGAGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCACC
AAAGCCAACCGTGTGTATGGGCCTCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTC
CACCAGAACTTTACAATCCTAATTTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACC
TGGCTCCCCATCTTTTGACCAACCCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAA
ATCAAGGTGGAAAAGGATGAATAAAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCC
ATGTCTCAGAAATAGGTGGCCATGGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGA
AAGCAAATTTGCCTCTTTTCTTAACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAA
AACTTATCTAGAAGGGGAGAAACTCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCT
CAGCATAAACAGTATCTCGGAGAAGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACA
TGAGGCCTTCTTGACATA

hide sequence

RefSeq Acc Id:

XM_011537059 ⟹ XP_011535361

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

CTTTTTGCACACACACGAATACAAAGAGCCATACGACCTTCGGGTATCCTTTTTCCATTTTTTT
TCCTCCTTAATCTTGTGTGTGTTTTCAAATTTTTTAAAAATAGAGATCTGTAGCAGTGTTGGGG
TTGCACTAGTCGGGGGTTCCATGCTGGGGGGCAGAAGGAATGCTCTCTACCGTCTGAAACCGTT
CATCAGGAAGGCCTTGATTTGTGATGTGCTAGGAGAGCACAGGATCTGCAAATAGAAGGCACCT
GTCTCCCTTCTGCAGGCCGAGGAGAGGCCGCCATGGACTGTGTGCTTCTTCATGGCTTGTTTAC
TCTTCTTTCACAGACCCTACAGCTTGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAGGA
AAGTGAGTCCAGAGAAGTTGATGCTTCCTACCTGTTGGAGCGGCCCAGCAGTGTAAGCGTGGTT
GTTACTGCCCCATCCGCCATGTCCTTCAGTGCCACCATTCTCTTCTCCCCTCCCAGTGGCAGCG
AGGCCAGATGCTGCTGCTGCGCCTGTAAGAGTGAGACTAATGGAGGCAACACAGGCTCCCAGGG
TGGGAATCCTCCTCCCAGCACCCCCATCACAGTGACTGGACATGGCTTGGCTGTTCAGAGCTCA
GAGCAGCTCCTGCATGTTATCTACCAGCGGGTCGATAAGGCAGTGGGTTTGGCTGAAGCTGCTC
TGGGTCTTGCCAGGGCCAACAATGAGTTGTTAAAACGTCTCCAGGAGGAAGTGGGTGACCTGAG
GCAAGGGAAAGTGTCCATCCCTGATGAAGATGGGGAAAGCCGGGCACATAGTTCCCCACCTGAG
GAGCCTGGGCCTCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGG
AGTGTGACAGCGTGGGCAGCGGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGC
CTCAGTGGGGCCTGGGCCTTTGGGCTTCCCAGCAACTCAGAGGGACATGCGGCTCCCAGGGTGC
ACGCTGGCTGCCAGCGAGGCGGCCCCCCTGCTCAATCCTCTGGTGGATGATTACGTGGCCTCTG
AGGGTGCAGTACAGCGAGTTCTGGTCCCTGCTTATGCCAAGCAACTCTCACCAGCCACACAACT
GGCAATCCAGCGGGCAACCCCAGAGACAGGACCAGAAAATGGAACCAAGCTGCCACCACCCCGC
CCTGAGGACATGCTCAATGCCGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGA
GCACTGGGGAGCTGAGACACTCTCTAGGGCTGACCGTTTCCCCATGCAGGACCAGAGGAAGTGG
GCAGAAGAACTCCAGGCGCAAGCGGGATCTTGTACTCTCTAAACTGGTCCACAATGTGCATAAC
CACATCACCAATGACAAGAGATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGGAATATTTCAG
TAGTGAAGTTTCTTCTGGAAAAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACAATTACACTGA
TAAGGAGCTAAAAGGAGCCTGTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTACCGCAACTCC
CTGAACCCCTTTAAAGGCCTGAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGCCGATATCGGC
TTTTTGCCAACCGATCCAGTATCATGAGGCATTTTGGACCTGAGGACCAACGTCTGTGGAATGA
TGTGACAGAGGAACTGATGTCAGATGAAGAGGACAGTCTTAACGAGCCAGGTGTGTGGGTGGCC
CGCCCTCCCCGTTTCCGGGCCCAGCGCCTCACAGAGCTCTGCTACCACCTGGATGCTAACTCTA
AGCATGGCACCAAAGCCAACCGTGTGTATGGGCCTCCCTCAGACAGACTGCCTTCTGCTGAAGC
CCAGCTCCTTCCACCAGAACTTTACAATCCTAATTTCCAAGAAGAGGAAGATGAGGGAGGGGAT
GAGAATGCACCTGGCTCCCCATCTTTTGACCAACCCCACAAAACCTGCTGTCCTGACTTGAACT
CATTCATTGAAATCAAGGTGGAAAAGGATGAATAAAATCTACAGCCAAGAATAACTCTGGCTTC
CGCCATGCCCCATGTCTCAGAAATAGGTGGCCATGGGGCTTCACAAAATAATGAGATGCTCTGT
GCAGTCTGAGAAAGCAAATTTGCCTCTTTTCTTAACACAGTCTCTACTGGGGAAGCAGAACACT
GGTGGGATAAAAACTTATCTAGAAGGGGAGAAACTCCCTCCACTGTGAACAGTAAGCCAGAATA
TGCTTATTCCTCAGCATAAACAGTATCTCGGAGAAGCCTGGGATGAGAAAATGAGGAGGATGGG
TCCAAGAAACATGAGGCCTTCTTGACA

hide sequence

RefSeq Acc Id:

XM_011537060 ⟹ XP_011535362

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

GGCAAACCTGAAATCGGAAATATTAATCTTACCAATGTAATCTTAGCAAATGTAAATAAAAAGG
ACTGTGCTATACTGGGCTAAAAATTCTCATCCTGCTATAGAAATATACGTGGAATTTTCAGATT
ACGTGGAATCCTTTAAAGACCGCATTCGGCCTTCTGGGTCTACAGCTCTCTTTTTTACCCCTAA
AAATAAGGTCTTGGATTTTTTGCAGACCATTAGTCGAGTCACTCTTTTAAAATGTGGGAAAATA
GTATTTTGTGGTATTTACTTAGCTGCTCTTGTGTGATAAGGAGCTCATTTCTGATAAAAATAGG
TTTTGAGAGAACCTTTTGACAGGTGAGCCATTTTGCACCTTGAAGTGGAGGAGTAGGACTGACC
AACACAGCAGGAGCTTTAAGTGGCCGTTTTCCTTATTTATTTCTTAAAATGAAGATTATGATAT
GAATTGCCATGCTTTCAGTAATCACATTTAAGGAAGTCTATTGCTAGCATGACCCTGAATGAGT
CAAGCACCCATTATAAAAACATATATCATCTGAGTGATACCATATCATACACATCTATTAAATA
GTGAGAAAACTTTTATTTTTCATAGTTTGGAGGTGAACTCAGTCATGCAGAAAATTCAAACTCA
GAATGGGGAGAAAGCAAGCAAGGGAACTGCCAAGAGTATGATATATTTAGTCCTAACAAAAATG
TGACTTGGGAGGAAAGGGATAGTTAAAATTATGGACAGTCTTACCCTGAACTGTCTGTCTAAAG
GAGATGAATTGTCTTTCTTTTTTATCTAAATATTTATGAAAAATACCAAAAGTACTGGAAAGTA
CATTTTTAAGGCTCGTTTCACATTTATTTAAATTAGACCAATACTGAAATGAACCCCAAATGCT
TATATTTTTTGCAAACCTAAGTGTGACATCTACTGTCATGTTGTGTTGGCAACGCATCCCAAGA
TTGAAGATCTTTTTCTCTTTTTTAGACCTAGTCAGTTGTTTTCAGGACTTTCTACTTAAACATG
TTGCCATCATTTGAAATTTAAAATGTTAAATAAATACACTTCTTCTCTAATATACTGGTGTCTC
CTCTTTTTATTTATTTATTTTTTAGAGACTGGGTCTTGCTATGCTGCCGAGGTTGGTCTCAAAC
TCCTGGGCTCAAGCGATCCTCCTCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCC
CAGCCATGGTATTTCCTCTCAACTGCCTCATTTCTGTCATTCTGGTGGTGGTGGTGGTACCATC
CTGTTACTCTTAGGCTTATAACCTTGCAGTTGTCTTTAACCAATTATCTCTATACCCCATCTCT
ATAACTCTGTCAATTCTCCTTATCTTACTATATAAGCGCCTTTGCTCTGACCTCTGACATGTAC
CCTGTTAAGTCCTGTAATTTTTTTTTTTTCCTCTAGAATGTCTTACTACCCTATCAGTTAATCC
TATACATTGCTCAAGGCTCAACTGGAAGCTTTTCTTCTTTTCAGGTTTAGCTGTGCCTCCCAGT
GACTATAATGACAAGGAAGCTGTAAATGTATTTGAGTTAAGCTTTTGCGAGAAACCCTACAGCT
TGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTTGATGC
TTCCTACCTGTTGGAGCGGCCCAGCAGTGTAAGCGTGGTTGTTACTGCCCCATCCGCCATGTCC
TTCAGTGCCACCATTCTCTTCTCCCCTCCCAGTGGCAGCGAGGCCAGATGCTGCTGCTGCGCCT
GTAAGAGTGAGACTAATGGAGGCAACACAGGCTCCCAGGGTGGGAATCCTCCTCCCAGCACCCC
CATCACAGTGACTGGACATGGCTTGGCTGTTCAGAGCTCAGAGCAGCTCCTGCATGTTATCTAC
CAGCGGGTCGATAAGGCAGTGGGTTTGGCTGAAGCTGCTCTGGGTCTTGCCAGGGCCAACAATG
AGTTGTTAAAACGTCTCCAGGAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTCCATCCCTGA
TGAAGATGGGGAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGT
CCCGGGGAAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGGGCAGCGGCG
TGCAGGTGGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGGGCCTTTGGG
CTTCCCAGCAACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGCGAGGCGGCC
CCCCTGCTCAATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGTACAGCGAGTTCTGG
TCCCTGCTTATGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAGCGGGCAACCCCAGA
GACAGGACCAGAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACATGCTCAATGCCGCT
GCTGCGCTGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGAGACACTCTC
TAGGGCTGACCGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAGGCGCAAGCG
GGATCTTGTACTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCAATGACAAGAGATTC
AATGGGTCTGAAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTCTGGAAAAGC
TCAAGCAAGAGCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTAAAAGGAGCCTGTGT
GGCCTACTTCCTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAAGGCCTGAAG
GAAAAAGAGGAGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAACCGATCCAGTATCA
TGAGGCATTTTGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAGGAACTGATGTCAGA
TGAAGAGGACAGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTTCCGGGCCCAG
CGCCTCACAGAGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCACCAAAGCCAACCGTG
TGTATGGGCCTCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACCAGAACTTTA
CAATCCTAATTTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACCTGGCTCCCCATCT
TTTGACCAACCCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAAATCAAGGTGGAAA
AGGATGAATAAAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCCATGTCTCAGAAAT
AGGTGGCCATGGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGCAAATTTGCC
TCTTTTCTTAACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAAAACTTATCTAGAA
GGGGAGAAACTCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCTCAGCATAAACAGT
ATCTCGGAGAAGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACATGAGGCCTTCTTG
ACA

hide sequence

RefSeq Acc Id:

XM_011537062 ⟹ XP_011535364

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

GCGGTAGCCGGGTACACGGGCAGGCGCCGCGGATAGTTCTGTCTCCCGCGCGCCCGCCTCCGCC
TCTGCCTAGCTGAGTCAGCCCGTGCGGTAGCGCCAGGCACACGCGGTAGAACATCTGTAGGGCT
GCAAAGCTGCACCTCCGCGTCAGTTCTCACGGCGAGCGCCGCCTTCAGCCCAAGTTCTCAAAGC
TCTCGGGGCTACGTAGTCTACCCTCCCCGGTGACCCGGCGAGATCCCTAGCCGCTCCTCCGGCC
GCTCTGCTCTCCGCATCCCTCGCGGGAATGACCCCCTTTACCCGGGACTCCCAGAGCGCACTGT
ATGACCCTACAGCTTGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCC
AGAGAAGTTGATGCTTCCTACCTGTTGGAGCGGCCCAGCAGTGTAAGCGTGGTTGTTACTGCCC
CATCCGCCATGTCCTTCAGTGCCACCATTCTCTTCTCCCCTCCCAGTGGCAGCGAGGCCAGATG
CTGCTGCTGCGCCTGTAAGAGTGAGACTAATGGAGGCAACACAGGCTCCCAGGGTGGGAATCCT
CCTCCCAGCACCCCCATCACAGTGACTGGACATGGCTTGGCTGTTCAGAGCTCAGAGCAGCTCC
TGCATGTTATCTACCAGCGGGTCGATAAGGCAGTGGGTTTGGCTGAAGCTGCTCTGGGTCTTGC
CAGGGCCAACAATGAGTTGTTAAAACGTCTCCAGGAGGAAGTGGGTGACCTGAGGCAAGGGAAA
GTGTCCATCCCTGATGAAGATGGGGAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGC
CTCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAG
CGTGGGCAGCGGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGG
CCTGGGCCTTTGGGCTTCCCAGCAACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTG
CCAGCGAGGCGGCCCCCCTGCTCAATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGT
ACAGCGAGTTCTGGTCCCTGCTTATGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAG
CGGGCAACCCCAGAGACAGGACCAGAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACA
TGCTCAATGCCGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGA
GCTGAGACACTCTCTAGGGCTGACCGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAAC
TCCAGGCGCAAGCGGGATCTTGTACTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCA
ATGACAAGAGATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTT
TCTTCTGGAAAAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTA
AAAGGAGCCTGTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCT
TTAAAGGCCTGAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAA
CCGATCCAGTATCATGAGGCATTTTGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAG
GAACTGATGTCAGATGAAGAGGACAGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCC
GTTTCCGGGCCCAGCGCCTCACAGAGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCAC
CAAAGCCAACCGTGTGTATGGGCCTCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTT
CCACCAGAACTTTACAATCCTAATTTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCAC
CTGGCTCCCCATCTTTTGACCAACCCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGA
AATCAAGGTGGAAAAGGATGAATAAAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCC
CATGTCTCAGAAATAGGTGGCCATGGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAG
AAAGCAAATTTGCCTCTTTTCTTAACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAA
AAACTTATCTAGAAGGGGAGAAACTCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCC
TCAGCATAAACAGTATCTCGGAGAAGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAAC
ATGAGGCCTTCTTGACA

hide sequence

RefSeq Acc Id:

XM_017021570 ⟹ XP_016877059

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

GGCAAACCTGAAATCGGAAATATTAATCTTACCAATGTAATCTTAGCAAATGTAAATAAAAAGG
ACTGTGCTATACTGGGCTAAAAATTCTCATCCTGCTATAGAAATATACGTGGAATTTTCAGATT
ACGTGGAATCCTTTAAAGACCGCATTCGGCCTTCTGGGTCTACAGCTCTCTTTTTTACCCCTAA
AAATAAGGTCTTGGATTTTTTGCAGACCATTAGTCGAGTCACTCTTTTAAAATGTGGGAAAATA
GTATTTTGTGGTATTTACTTAGCTGCTCTTGTGTGATAAGGAGCTCATTTCTGATAAAAATAGG
TTTTGAGAGAACCTTTTGACAGGTGAGCCATTTTGCACCTTGAAGTGGAGGAGTAGGACTGACC
AACACAGCAGGAGCTTTAAGTGGCCGTTTTCCTTATTTATTTCTTAAAATGAAGATTATGATAT
GAATTGCCATGCTTTCAGTAATCACATTTAAGGAAGTCTATTGCTAGCATGACCCTGAATGAGT
CAAGCACCCATTATAAAAACATATATCATCTGAGTGATACCATATCATACACATCTATTAAATA
GTGAGAAAACTTTTATTTTTCATAGTTTGGAGGTGAACTCAGTCATGCAGAAAATTCAAACTCA
GAATGGGGAGAAAGCAAGCAAGGGAACTGCCAAGAGTATGATATATTTAGTCCTAACAAAAATG
TGACTTGGGAGGAAAGGGATAGTTAAAATTATGGACAGTCTTACCCTGAACTGTCTGTCTAAAG
GAGATGAATTGTCTTTCTTTTTTATCTAAATATTTATGAAAAATACCAAAAGTACTGGAAAGTA
CATTTTTAAGGCTCGTTTCACATTTATTTAAATTAGACCAATACTGAAATGAACCCCAAATGCT
TATATTTTTTGCAAACCTAAGTGTGACATCTACTGTCATGTTGTGTTGGCAACGCATCCCAAGA
TTGAAGATCTTTTTCTCTTTTTTAGACCTAGTCAGTTGTTTTCAGGACTTTCTACTTAAACATG
TTGCCATCATTTGAAATTTAAAATGTTAAATAAATACACTTCTTCTCTAATATACTGGTGTCTC
CTCTTTTTATTTATTTATTTTTTAGAGACTGGGTCTTGCTATGCTGCCGAGGTTGGTCTCAAAC
TCCTGGGCTCAAGCGATCCTCCTCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCC
CAGCCATGGTATTTCCTCTCAACTGCCTCATTTCTGTCATTCTGGTGGTGGTGGTGGTACCATC
CTGTTACTCTTAGGCTTATAACCTTGCAGTTGTCTTTAACCAATTATCTCTATACCCCATCTCT
ATAACTCTGTCAATTCTCCTTATCTTACTATATAAGCGCCTTTGCTCTGACCTCTGACATGTAC
CCTGTTAAGTCCTGTAATTTTTTTTTTTTCCTCTAGAATGTCTTACTACCCTATCAGTTAATCC
TATACATTGCTCAAGGCTCAACTGGAAGCTTTTCTTCTTTTCAGGTTTAGCTGTGCCTCCCAGT
GACTATAATGACAAGGAAGCTGTAAATGTATTTGAGTTAAGCTTTTGCGAGAAATGCCGGAAGG
TCCTTCTGAATCCCTTCCCTGTTCCTTAGGTTGCACTAGTCGGGGGTTCCATGCTGGGGGGCAG
AAGGAATGCTCTCTACCGTCTGAAACCGTTCATCAGGAAGGCCTTGATTTGTGATGTGCTAGGA
GAGCACAGGATCTGCAAATAGAAGGCACCTGTCTCCCTTCTGCAGGCCGAGGAGAGGCCGCCAT
GGACTGTGTGCTTCTTCATGGCTTGTTTACTCTTCTTTCACAGACCCTACAGCTTGGGGCCTGG
GCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTTGATGCTTCCTACCTG
TTGGAGCGGCCCAGCAGTGTAAGCGTGGTTGTTACTGCCCCATCCGCCATGTCCTTCAGTGCCA
CCATTCTCTTCTCCCCTCCCAGTGGCAGCGAGGCCAGATGCTGCTGCTGCGCCTGTAAGAGTGA
GACTAATGGAGGCAACACAGGCTCCCAGGGTGGGAATCCTCCTCCCAGCACCCCCATCACAGTG
ACTGGACATGGCTTGGCTGTTCAGAGCTCAGAGCAGCTCCTGCATGTTATCTACCAGCGGGTCG
ATAAGGCAGTGGGTTTGGCTGAAGCTGCTCTGGGTCTTGCCAGGGCCAACAATGAGTTGTTAAA
ACGTCTCCAGGAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTCCATCCCTGATGAAGATGGG
GAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGTCCCGGGGAAG
CCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGGGCAGCGGCGTGCAGGTGGT
GATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGGGCCTTTGGGCTTCCCAGCA
ACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGCGAGGCGGCCCCCCTGCTCA
ATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGTACAGCGAGTTCTGGTCCCTGCTTA
TGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAGCGGGCAACCCCAGAGACAGGACCA
GAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACATGCTCAATGCCGCTGCTGCGCTGG
ACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGAGACACTCTCTAGGGCTGAC
CGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAGGCGCAAGCGGGATCTTGTA
CTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCAATGACAAGAGATTCAATGGGTCTG
AAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTCTGGAAAAGCTCAAGCAAGA
GCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTAAAAGGAGCCTGTGTGGCCTACTTC
CTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAAGGCCTGAAGGAAAAAGAGG
AGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAACCGATCCAGTATCATGAGGCATTT
TGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAGGAACTGATGTCAGATGAAGAGGAC
AGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTTCCGGGCCCAGCGCCTCACAG
AGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCACCAAAGCCAACCGTGTGTATGGGCC
TCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACCAGAACTTTACAATCCTAAT
TTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACCTGGCTCCCCATCTTTTGACCAAC
CCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAAATCAAGGTGGAAAAGGATGAATA
AAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCCATGTCTCAGAAATAGGTGGCCAT
GGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGCAAATTTGCCTCTTTTCTTA
ACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAAAACTTATCTAGAAGGGGAGAAAC
TCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCTCAGCATAAACAGTATCTCGGAGA
AGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACATGAGGCCTTCTTGACA

hide sequence

RefSeq Acc Id:

XM_017021572 ⟹ XP_016877061

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

GGCAAACCTGAAATCGGAAATATTAATCTTACCAATGTAATCTTAGCAAATGTAAATAAAAAGG
ACTGTGCTATACTGGGCTAAAAATTCTCATCCTGCTATAGAAATATACGTGGAATTTTCAGATT
ACGTGGAATCCTTTAAAGACCGCATTCGGCCTTCTGGGTCTACAGCTCTCTTTTTTACCCCTAA
AAATAAGGTCTTGGATTTTTTGCAGACCATTAGTCGAGTCACTCTTTTAAAATGTGGGAAAATA
GTATTTTGTGGTATTTACTTAGCTGCTCTTGTGTGATAAGGAGCTCATTTCTGATAAAAATAGG
TTTTGAGAGAACCTTTTGACAGGTGAGCCATTTTGCACCTTGAAGTGGAGGAGTAGGACTGACC
AACACAGCAGGAGCTTTAAGTGGCCGTTTTCCTTATTTATTTCTTAAAATGAAGATTATGATAT
GAATTGCCATGCTTTCAGTAATCACATTTAAGGAAGTCTATTGCTAGCATGACCCTGAATGAGT
CAAGCACCCATTATAAAAACATATATCATCTGAGTGATACCATATCATACACATCTATTAAATA
GTGAGAAAACTTTTATTTTTCATAGTTTGGAGGTGAACTCAGTCATGCAGAAAATTCAAACTCA
GAATGGGGAGAAAGCAAGCAAGGGAACTGCCAAGAGTATGATATATTTAGTCCTAACAAAAATG
TGACTTGGGAGGAAAGGGATAGTTAAAATTATGGACAGTCTTACCCTGAACTGTCTGTCTAAAG
GAGATGAATTGTCTTTCTTTTTTATCTAAATATTTATGAAAAATACCAAAAGTACTGGAAAGTA
CATTTTTAAGGCTCGTTTCACATTTATTTAAATTAGACCAATACTGAAATGAACCCCAAATGCT
TATATTTTTTGCAAACCTAAGTGTGACATCTACTGTCATGTTGTGTTGGCAACGCATCCCAAGA
TTGAAGATCTTTTTCTCTTTTTTAGACCTAGTCAGTTGTTTTCAGGACTTTCTACTTAAACATG
TTGCCATCATTTGAAATTTAAAATGTTAAATAAATACACTTCTTCTCTAATATACTGGTGTCTC
CTCTTTTTATTTATTTATTTTTTAGAGACTGGGTCTTGCTATGCTGCCGAGGTTGGTCTCAAAC
TCCTGGGCTCAAGCGATCCTCCTCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCC
CAGCCATGGTATTTCCTCTCAACTGCCTCATTTCTGTCATTCTGGTGGTGGTGGTGGTACCATC
CTGTTACTCTTAGGCTTATAACCTTGCAGTTGTCTTTAACCAATTATCTCTATACCCCATCTCT
ATAACTCTGTCAATTCTCCTTATCTTACTATATAAGCGCCTTTGCTCTGACCTCTGACATGTAC
CCTGTTAAGTCCTGTAATTTTTTTTTTTTCCTCTAGAATGTCTTACTACCCTATCAGTTAATCC
TATACATTGCTCAAGGCTCAACTGGAAGCTTTTCTTCTTTTCAGGTTTAGCTGTGCCTCCCAGT
GACTATAATGACAAGGAAGCTGTAAATGTATTTGAGTTAAGCTTTTGCGAGAAGTTGCACTAGT
CGGGGGTTCCATGCTGGGGGGCAGAAGGAATGCTCTCTACCGTCTGAAACCGTTCATCAGGAAG
GCCTTGATTTGTGATGTGCTAGGAGAGCACAGGATCTGCAAATAGAAGGCACCTGTCTCCCTTC
TGCAGGCCGAGGAGAGGCCGCCATGGACTGTGTGCTTCTTCATGGCTTGTTTACTCTTCTTTCA
CAGACCCTACAGCTTGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCC
AGAGAAGTTGATGCTTCCTACCTGTTGGAGCGGCCCAGCAGTGTAAGCGTGGTTGTTACTGCCC
CATCCGCCATGTCCTTCAGTGCCACCATTCTCTTCTCCCCTCCCAGTGGCAGCGAGGCCAGATG
CTGCTGCTGCGCCTGTAAGAGTGAGACTAATGGAGGCAACACAGGCTCCCAGGGTGGGAATCCT
CCTCCCAGCACCCCCATCACAGTGACTGGACATGGCTTGGCTGTTCAGAGCTCAGAGCAGCTCC
TGCATGTTATCTACCAGCGGGTCGATAAGGCAGTGGGTTTGGCTGAAGCTGCTCTGGGTCTTGC
CAGGGCCAACAATGAGTTGTTAAAACGTCTCCAGGAGGAAGTGGGTGACCTGAGGCAAGGGAAA
GTGTCCATCCCTGATGAAGATGGGGAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGC
CTCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAG
CGTGGGCAGCGGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGG
CCTGGGCCTTTGGGCTTCCCAGCAACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTG
CCAGCGAGGCGGCCCCCCTGCTCAATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGT
ACAGCGAGTTCTGGTCCCTGCTTATGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAG
CGGGCAACCCCAGAGACAGGACCAGAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACA
TGCTCAATGCCGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGA
GCTGAGACACTCTCTAGGGCTGACCGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAAC
TCCAGGCGCAAGCGGGATCTTGTACTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCA
ATGACAAGAGATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTT
TCTTCTGGAAAAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTA
AAAGGAGCCTGTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCT
TTAAAGGCCTGAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAA
CCGATCCAGTATCATGAGGCATTTTGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAG
GAACTGATGTCAGATGAAGAGGACAGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCC
GTTTCCGGGCCCAGCGCCTCACAGAGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCAC
CAAAGCCAACCGTGTGTATGGGCCTCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTT
CCACCAGAACTTTACAATCCTAATTTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCAC
CTGGCTCCCCATCTTTTGACCAACCCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGA
AATCAAGGTGGAAAAGGATGAATAAAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCC
CATGTCTCAGAAATAGGTGGCCATGGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAG
AAAGCAAATTTGCCTCTTTTCTTAACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAA
AAACTTATCTAGAAGGGGAGAAACTCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCC
TCAGCATAAACAGTATCTCGGAGAAGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAAC
ATGAGGCCTTCTTGACA

hide sequence

RefSeq Acc Id:

XM_017021573 ⟹ XP_016877062

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

ACGAATACAAAGAGCCATACGACCTTCGGTTTCAGGTTTAGCTGTGCCTCCCAGTGACTATAAT
GACAAGGAAGCTGTAAATGTATTTGAGTTAAGCTTTTGCGAGAAATGCCGGAAGGTCCTTCTGA
ATCCCTTCCCTGTTCCTTAGGTTGCACTAGTCGGGGGTTCCATGCTGGGGGGCAGAAGGAATGC
TCTCTACCGTCTGAAACCGTTCATCAGGAAGGCCTTGATTTGTGATGTGCTAGGAGAGCACAGG
ATCTGCAAATAGAAGGCACCTGTCTCCCTTCTGCAGGCCGAGGAGAGGCCGCCATGGACTGTGT
GCTTCTTCATGGCTTGTTTACTCTTCTTTCACAGACCCTACAGCTTGGGGCCTGGGCTCCTCTG
ACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTTGATGCTTCCTACCTGTTGGAGCGG
CCCAGCAGTGTAAGCGTGGTTGTTACTGCCCCATCCGCCATGTCCTTCAGTGCCACCATTCTCT
TCTCCCCTCCCAGTGGCAGCGAGGCCAGATGCTGCTGCTGCGCCTGTAAGAGTGAGACTAATGG
AGGCAACACAGGCTCCCAGGGTGGGAATCCTCCTCCCAGCACCCCCATCACAGTGACTGGACAT
GGCTTGGCTGTTCAGAGCTCAGAGCAGCTCCTGCATGTTATCTACCAGCGGGTCGATAAGGCAG
TGGGTTTGGCTGAAGCTGCTCTGGGTCTTGCCAGGGCCAACAATGAGTTGTTAAAACGTCTCCA
GGAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTCCATCCCTGATGAAGATGGGGAAAGCCGG
GCACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGG
CTCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGGGCAGCGGCGTGCAGGTGGTGATTGAGGA
GCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGGGCCTTTGGGCTTCCCAGCAACTCAGAGG
GACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGCGAGGCGGCCCCCCTGCTCAATCCTCTGG
TGGATGATTACGTGGCCTCTGAGGGTGCAGTACAGCGAGTTCTGGTCCCTGCTTATGCCAAGCA
ACTCTCACCAGCCACACAACTGGCAATCCAGCGGGCAACCCCAGAGACAGGACCAGAAAATGGA
ACCAAGCTGCCACCACCCCGCCCTGAGGACATGCTCAATGCCGCTGCTGCGCTGGACAGTGCCT
TGGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGAGACACTCTCTAGGGCTGACCGTTTCCCC
ATGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAGGCGCAAGCGGGATCTTGTACTCTCTAAA
CTGGTCCACAATGTGCATAACCACATCACCAATGACAAGAGATTCAATGGGTCTGAAAGCATCA
AGTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTCTGGAAAAGCTCAAGCAAGAGCTGGTGAC
CAGTCCCCACAATTACACTGATAAGGAGCTAAAAGGAGCCTGTGTGGCCTACTTCCTTACTAAG
AGGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAAGGCCTGAAGGAAAAAGAGGAGAAGAAAC
TTCGAAGTCGCCGATATCGGCTTTTTGCCAACCGATCCAGTATCATGAGGCATTTTGGACCTGA
GGACCAACGTCTGTGGAATGATGTGACAGAGGAACTGATGTCAGATGAAGAGGACAGTCTTAAC
GAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTTCCGGGCCCAGCGCCTCACAGAGCTCTGCT
ACCACCTGGATGCTAACTCTAAGCATGGCACCAAAGCCAACCGTGTGTATGGGCCTCCCTCAGA
CAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACCAGAACTTTACAATCCTAATTTCCAAGAA
GAGGAAGATGAGGGAGGGGATGAGAATGCACCTGGCTCCCCATCTTTTGACCAACCCCACAAAA
CCTGCTGTCCTGACTTGAACTCATTCATTGAAATCAAGGTGGAAAAGGATGAATAAAATCTACA
GCCAAGAATAACTCTGGCTTCCGCCATGCCCCATGTCTCAGAAATAGGTGGCCATGGGGCTTCA
CAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGCAAATTTGCCTCTTTTCTTAACACAGTCT
CTACTGGGGAAGCAGAACACTGGTGGGATAAAAACTTATCTAGAAGGGGAGAAACTCCCTCCAC
TGTGAACAGTAAGCCAGAATATGCTTATTCCTCAGCATAAACAGTATCTCGGAGAAGCCTGGGA
TGAGAAAATGAGGAGGATGGGTCCAAGAAACATGAGGCCTTCTTGACA

hide sequence

RefSeq Acc Id:

XM_017021574 ⟹ XP_016877063

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

GGCAAACCTGAAATCGGAAATATTAATCTTACCAATGTAATCTTAGCAAATGTAAATAAAAAGG
ACTGTGCTATACTGGGCTAAAAATTCTCATCCTGCTATAGAAATATACGTGGAATTTTCAGATT
ACGTGGAATCCTTTAAAGACCGCATTCGGCCTTCTGGGTCTACAGCTCTCTTTTTTACCCCTAA
AAATAAGGTCTTGGATTTTTTGCAGACCATTAGTCGAGTCACTCTTTTAAAATGTGGGAAAATA
GTATTTTGTGGTATTTACTTAGCTGCTCTTGTGTGATAAGGAGCTCATTTCTGATAAAAATAGG
TTTTGAGAGAACCTTTTGACAGGTGAGCCATTTTGCACCTTGAAGTGGAGGAGTAGGACTGACC
AACACAGCAGGAGCTTTAAGTGGCCGTTTTCCTTATTTATTTCTTAAAATGAAGATTATGATAT
GAATTGCCATGCTTTCAGTAATCACATTTAAGGAAGTCTATTGCTAGCATGACCCTGAATGAGT
CAAGCACCCATTATAAAAACATATATCATCTGAGTGATACCATATCATACACATCTATTAAATA
GTGAGAAAACTTTTATTTTTCATAGTTTGGAGGTGAACTCAGTCATGCAGAAAATTCAAACTCA
GAATGGGGAGAAAGCAAGCAAGGGAACTGCCAAGAGTATGATATATTTAGTCCTAACAAAAATG
TGACTTGGGAGGAAAGGGATAGTTAAAATTATGGACAGTCTTACCCTGAACTGTCTGTCTAAAG
GAGATGAATTGTCTTTCTTTTTTATCTAAATATTTATGAAAAATACCAAAAGTACTGGAAAGTA
CATTTTTAAGGCTCGTTTCACATTTATTTAAATTAGACCAATACTGAAATGAACCCCAAATGCT
TATATTTTTTGCAAACCTAAGTGTGACATCTACTGTCATGTTGTGTTGGCAACGCATCCCAAGA
TTGAAGATCTTTTTCTCTTTTTTAGACCTAGTCAGTTGTTTTCAGGACTTTCTACTTAAACATG
TTGCCATCATTTGAAATTTAAAATGTTAAATAAATACACTTCTTCTCTAATATACTGGTGTCTC
CTCTTTTTATTTATTTATTTTTTAGAGACTGGGTCTTGCTATGCTGCCGAGGTTGGTCTCAAAC
TCCTGGGCTCAAGCGATCCTCCTCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCC
CAGCCATGGTATTTCCTCTCAACTGCCTCATTTCTGTCATTCTGGTGGTGGTGGTGGTACCATC
CTGTTACTCTTAGGCTTATAACCTTGCAGTTGTCTTTAACCAATTATCTCTATACCCCATCTCT
ATAACTCTGTCAATTCTCCTTATCTTACTATATAAGCGCCTTTGCTCTGACCTCTGACATGTAC
CCTGTTAAGTCCTGTAATTTTTTTTTTTTCCTCTAGAATGTCTTACTACCCTATCAGTTAATCC
TATACATTGCTCAAGGCTCAACTGGAAGCTTTTCTTCTTTTCAGGTTTAGCTGTGCCTCCCAGT
GACTATAATGACAAGGAAGCTGTAAATGTATTTGAGTTAAGCTTTTGCGAGAAGCAAAGTGACA
GCATAGCTGTTCAAACATTCCTGTTGAATTTTGGATCCACCCTTAAGGAGCTTGAGAAATGAAG
ATAAGGGGCCCCACGGGTGATTTCTCTGGGCTCCTGGCTGGAAGATTCAGGACAGCTAGTTTCC
ATTACAGAGGCTCATGGCCCAGACCCTACAGCTTGGGGCCTGGGCTCCTCTGACCATCCTCATT
GAGAAAGGAAAGTGAGTCCAGAGAAGTTGATGCTTCCTACCTGTTGGAGCGGCCCAGCAGTGTA
AGCGTGGTTGTTACTGCCCCATCCGCCATGTCCTTCAGTGCCACCATTCTCTTCTCCCCTCCCA
GTGGCAGCGAGGCCAGATGCTGCTGCTGCGCCTGTAAGAGTGAGACTAATGGAGGCAACACAGG
CTCCCAGGGTGGGAATCCTCCTCCCAGCACCCCCATCACAGTGACTGGACATGGCTTGGCTGTT
CAGAGCTCAGAGCAGCTCCTGCATGTTATCTACCAGCGGGTCGATAAGGCAGTGGGTTTGGCTG
AAGCTGCTCTGGGTCTTGCCAGGGCCAACAATGAGTTGTTAAAACGTCTCCAGGAGGAAGTGGG
TGACCTGAGGCAAGGGAAAGTGTCCATCCCTGATGAAGATGGGGAAAGCCGGGCACATAGTTCC
CCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCCG
TGGAAGAGGAGTGTGACAGCGTGGGCAGCGGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGCT
GGGAGCAGCCTCAGTGGGGCCTGGGCCTTTGGGCTTCCCAGCAACTCAGAGGGACATGCGGCTC
CCAGGGTGCACGCTGGCTGCCAGCGAGGCGGCCCCCCTGCTCAATCCTCTGGTGGATGATTACG
TGGCCTCTGAGGGTGCAGTACAGCGAGTTCTGGTCCCTGCTTATGCCAAGCAACTCTCACCAGC
CACACAACTGGCAATCCAGCGGGCAACCCCAGAGACAGGACCAGAAAATGGAACCAAGCTGCCA
CCACCCCGCCCTGAGGACATGCTCAATGCCGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCAG
GCCCTGGGAGCACTGGGGAGCTGAGACACTCTCTAGGGCTGACCGTTTCCCCATGCAGGACCAG
AGGAAGTGGGCAGAAGAACTCCAGGCGCAAGCGGGATCTTGTACTCTCTAAACTGGTCCACAAT
GTGCATAACCACATCACCAATGACAAGAGATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGGA
ATATTTCAGTAGTGAAGTTTCTTCTGGAAAAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACAA
TTACACTGATAAGGAGCTAAAAGGAGCCTGTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTAC
CGCAACTCCCTGAACCCCTTTAAAGGCCTGAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGCC
GATATCGGCTTTTTGCCAACCGATCCAGTATCATGAGGCATTTTGGACCTGAGGACCAACGTCT
GTGGAATGATGTGACAGAGGAACTGATGTCAGATGAAGAGGACAGTCTTAACGAGCCAGGTGTG
TGGGTGGCCCGCCCTCCCCGTTTCCGGGCCCAGCGCCTCACAGAGCTCTGCTACCACCTGGATG
CTAACTCTAAGCATGGCACCAAAGCCAACCGTGTGTATGGGCCTCCCTCAGACAGACTGCCTTC
TGCTGAAGCCCAGCTCCTTCCACCAGAACTTTACAATCCTAATTTCCAAGAAGAGGAAGATGAG
GGAGGGGATGAGAATGCACCTGGCTCCCCATCTTTTGACCAACCCCACAAAACCTGCTGTCCTG
ACTTGAACTCATTCATTGAAATCAAGGTGGAAAAGGATGAATAAAATCTACAGCCAAGAATAAC
TCTGGCTTCCGCCATGCCCCATGTCTCAGAAATAGGTGGCCATGGGGCTTCACAAAATAATGAG
ATGCTCTGTGCAGTCTGAGAAAGCAAATTTGCCTCTTTTCTTAACACAGTCTCTACTGGGGAAG
CAGAACACTGGTGGGATAAAAACTTATCTAGAAGGGGAGAAACTCCCTCCACTGTGAACAGTAA
GCCAGAATATGCTTATTCCTCAGCATAAACAGTATCTCGGAGAAGCCTGGGATGAGAAAATGAG
GAGGATGGGTCCAAGAAACATGAGGCCTTCTTGACA

hide sequence

RefSeq Acc Id:

XM_017021575 ⟹ XP_016877064

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

GGCAAACCTGAAATCGGAAATATTAATCTTACCAATGTAATCTTAGCAAATGTAAATAAAAAGG
ACTGTGCTATACTGGGCTAAAAATTCTCATCCTGCTATAGAAATATACGTGGAATTTTCAGATT
ACGTGGAATCCTTTAAAGACCGCATTCGGCCTTCTGGGTCTACAGCTCTCTTTTTTACCCCTAA
AAATAAGGTCTTGGATTTTTTGCAGACCATTAGTCGAGTCACTCTTTTAAAATGTGGGAAAATA
GTATTTTGTGGTATTTACTTAGCTGCTCTTGTGTGATAAGGAGCTCATTTCTGATAAAAATAGG
TTTTGAGAGAACCTTTTGACAGGTGAGCCATTTTGCACCTTGAAGTGGAGGAGTAGGACTGACC
AACACAGCAGGAGCTTTAAGTGGCCGTTTTCCTTATTTATTTCTTAAAATGAAGATTATGATAT
GAATTGCCATGCTTTCAGTAATCACATTTAAGGAAGTCTATTGCTAGCATGACCCTGAATGAGT
CAAGCACCCATTATAAAAACATATATCATCTGAGTGATACCATATCATACACATCTATTAAATA
GTGAGAAAACTTTTATTTTTCATAGTTTGGAGGTGAACTCAGTCATGCAGAAAATTCAAACTCA
GAATGGGGAGAAAGCAAGCAAGGGAACTGCCAAGAGTATGATATATTTAGTCCTAACAAAAATG
TGACTTGGGAGGAAAGGGATAGTTAAAATTATGGACAGTCTTACCCTGAACTGTCTGTCTAAAG
GAGATGAATTGTCTTTCTTTTTTATCTAAATATTTATGAAAAATACCAAAAGTACTGGAAAGTA
CATTTTTAAGGCTCGTTTCACATTTATTTAAATTAGACCAATACTGAAATGAACCCCAAATGCT
TATATTTTTTGCAAACCTAAGTGTGACATCTACTGTCATGTTGTGTTGGCAACGCATCCCAAGA
TTGAAGATCTTTTTCTCTTTTTTAGACCTAGTCAGTTGTTTTCAGGACTTTCTACTTAAACATG
TTGCCATCATTTGAAATTTAAAATGTTAAATAAATACACTTCTTCTCTAATATACTGGTGTCTC
CTCTTTTTATTTATTTATTTTTTAGAGACTGGGTCTTGCTATGCTGCCGAGGTTGGTCTCAAAC
TCCTGGGCTCAAGCGATCCTCCTCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCC
CAGCCATGGTATTTCCTCTCAACTGCCTCATTTCTGTCATTCTGGTGGTGGTGGTGGTACCATC
CTGTTACTCTTAGGCTTATAACCTTGCAGTTGTCTTTAACCAATTATCTCTATACCCCATCTCT
ATAACTCTGTCAATTCTCCTTATCTTACTATATAAGCGCCTTTGCTCTGACCTCTGACATGTAC
CCTGTTAAGTCCTGTAATTTTTTTTTTTTCCTCTAGAATGTCTTACTACCCTATCAGTTAATCC
TATACATTGCTCAAGGCTCAACTGGAAGCTTTTCTTCTTTTCAGGTTTAGCTGTGCCTCCCAGT
GACTATAATGACAAGGAAGCTGTAAATGTATTTGAGTTAAGCTTTTGCGAGAAGCAAAGTGACA
GCATAGCTGTTCAAACATTCCTGTTGAATTTTGGATCCACCCTTAAGGAGCTTGAGAAATGAAG
ATAAGGGGCCCCACGGGTGATTTCTCTGGGCTCCTGGCTGGAAGATTCAGGACAGCTAGTTTCC
ATTACAGAGGCTCATGGCCCAGGTACACGACTATGTGGGAAAGGGGGCTGTGCAGCCCTGGGTT
ACCCCAGCTCAATTCCCTGATCTTTTCATTTCATTTCCCTGCCCTCATCCCCAAAGCATTAATG
ATATAATATAACAGTGAGAAGTTGGTGACATGCTGAGGGCTGCAGTGATGGATGTATTCCTTAT
TTAGGAGTGTTACTCTGAATGCATTTGTATGAAAATTACAGAGAGGGTAGAATCATGATTGTCA
TGATTGTTAATGTCAACAAAAAGTGGTATCAGTTAAAAAAAAATACAACACTACATTGAAAGTA
GCAATAACTGGATTCTGCTGTTATTCCTCTGACCTTGAAAAAGACATATAACTTCTCCACATGT
CTCTTCTCTGGACCTGGAGTAATATGTTTCCTAGTGCTGTTGAGTAGATGAGGTAACTTATGTG
AAGTGTTCTGAACACCTTAAGGAACAATGTCAAAGCAATGAAATGCAGTACCATTATTACAGTA
AAGATGGTGAGGAGGAGGAGGAGACAGATCTACATTTTCTTCCTTAATCTTCTAATCTTTCCAG
ATGCCGGAAGGTCCTTCTGAATCCCTTCCCTGTTCCTTAGGTTGCACTAGTCGGGGGTTCCATG
CTGGGGGGCAGAAGGAATGCTCTCTACCGTCTGAAACCGTTCATCAGGAAGGCCTTGATTTGTG
ATGTGCTAGGAGAGCACAGGATCTGCAAATAGAAGGCACCTGTCTCCCTTCTGCAGGCCGAGGA
GAGGCCGCCATGGACTGTGTGCTTCTTCATGGCTTGTTTACTCTTCTTTCACAGACCCTACAGC
TTGGGGCCTGGGCTCCTCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTTGATG
CTTCCTACCTGTTGGAGCGGCCCAGCAGTGAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTC
CATCCCTGATGAAGATGGGGAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTC
AAGGAAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGG
GCAGCGGCGTGCAGGTGGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGG
GCCTTTGGGCTTCCCAGCAACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGC
GAGGCGGCCCCCCTGCTCAATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGTACAGC
GAGTTCTGGTCCCTGCTTATGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAGCGGGC
AACCCCAGAGACAGGACCAGAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACATGCTC
AATGCCGCTGCTGCGCTGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGA
GACACTCTCTAGGGCTGACCGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAG
GCGCAAGCGGGATCTTGTACTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCAATGAC
AAGAGATTCAATGGGTCTGAAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTC
TGGAAAAGCTCAAGCAAGAGCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTAAAAGG
AGCCTGTGTGGCCTACTTCCTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAA
GGCCTGAAGGAAAAAGAGGAGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAACCGAT
CCAGTATCATGAGGCATTTTGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAGGAACT
GATGTCAGATGAAGAGGACAGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTTC
CGGGCCCAGCGCCTCACAGAGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCACCAAAG
CCAACCGTGTGTATGGGCCTCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACC
AGAACTTTACAATCCTAATTTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACCTGGC
TCCCCATCTTTTGACCAACCCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAAATCA
AGGTGGAAAAGGATGAATAAAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCCATGT
CTCAGAAATAGGTGGCCATGGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGC
AAATTTGCCTCTTTTCTTAACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAAAACT
TATCTAGAAGGGGAGAAACTCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCTCAGC
ATAAACAGTATCTCGGAGAAGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACATGAG
GCCTTCTTGACA

hide sequence

RefSeq Acc Id:

XM_017021576 ⟹ XP_016877065

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

Sequence:

show sequence

ACACACGAATACAAAGAGCCATACGACCTTCGGTTTCAGGTTTAGCTGTGCCTCCCAGTGACTA
TAATGACAAGGAAGCTGTAAATGTATTTGAGTTAAGCTTTTGCGAGAAATGCCGGAAGGTCCTT
CTGAATCCCTTCCCTGTTCCTTAGGTTGCACTAGTCGGGGGTTCCATGCTGGGGGGCAGAAGGA
ATGCTCTCTACCGTCTGAAACCGTTCATCAGGAAGGCCTTGATTTGTGATGTGCTAGGAGAGCA
CAGGATCTGCAAATAGAAGGCACCTGTCTCCCTTCTGCAGGCCGAGGAGAGGCCGCCATGGACT
GTGTGCTTCTTCATGGCTTGTTTACTCTTCTTTCACAGACCCTACAGCTTGGGGCCTGGGCTCC
TCTGACCATCCTCATTGAGAAAGGAAAGTGAGTCCAGAGAAGTTGATGCTTCCTACCTGTTGGA
GCGGCCCAGCAGTGAGGAAGTGGGTGACCTGAGGCAAGGGAAAGTGTCCATCCCTGATGAAGAT
GGGGAAAGCCGGGCACATAGTTCCCCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGTCCCGGGG
AAGCCTTTAAGGCTCTGTCTGCCGTGGAAGAGGAGTGTGACAGCGTGGGCAGCGGCGTGCAGGT
GGTGATTGAGGAGCTGCGGCAGCTGGGAGCAGCCTCAGTGGGGCCTGGGCCTTTGGGCTTCCCA
GCAACTCAGAGGGACATGCGGCTCCCAGGGTGCACGCTGGCTGCCAGCGAGGCGGCCCCCCTGC
TCAATCCTCTGGTGGATGATTACGTGGCCTCTGAGGGTGCAGTACAGCGAGTTCTGGTCCCTGC
TTATGCCAAGCAACTCTCACCAGCCACACAACTGGCAATCCAGCGGGCAACCCCAGAGACAGGA
CCAGAAAATGGAACCAAGCTGCCACCACCCCGCCCTGAGGACATGCTCAATGCCGCTGCTGCGC
TGGACAGTGCCTTGGAAGAGTCAGGCCCTGGGAGCACTGGGGAGCTGAGACACTCTCTAGGGCT
GACCGTTTCCCCATGCAGGACCAGAGGAAGTGGGCAGAAGAACTCCAGGCGCAAGCGGGATCTT
GTACTCTCTAAACTGGTCCACAATGTGCATAACCACATCACCAATGACAAGAGATTCAATGGGT
CTGAAAGCATCAAGTCCTCTTGGAATATTTCAGTAGTGAAGTTTCTTCTGGAAAAGCTCAAGCA
AGAGCTGGTGACCAGTCCCCACAATTACACTGATAAGGAGCTAAAAGGAGCCTGTGTGGCCTAC
TTCCTTACTAAGAGGCGTGAGTACCGCAACTCCCTGAACCCCTTTAAAGGCCTGAAGGAAAAAG
AGGAGAAGAAACTTCGAAGTCGCCGATATCGGCTTTTTGCCAACCGATCCAGTATCATGAGGCA
TTTTGGACCTGAGGACCAACGTCTGTGGAATGATGTGACAGAGGAACTGATGTCAGATGAAGAG
GACAGTCTTAACGAGCCAGGTGTGTGGGTGGCCCGCCCTCCCCGTTTCCGGGCCCAGCGCCTCA
CAGAGCTCTGCTACCACCTGGATGCTAACTCTAAGCATGGCACCAAAGCCAACCGTGTGTATGG
GCCTCCCTCAGACAGACTGCCTTCTGCTGAAGCCCAGCTCCTTCCACCAGAACTTTACAATCCT
AATTTCCAAGAAGAGGAAGATGAGGGAGGGGATGAGAATGCACCTGGCTCCCCATCTTTTGACC
AACCCCACAAAACCTGCTGTCCTGACTTGAACTCATTCATTGAAATCAAGGTGGAAAAGGATGA
ATAAAATCTACAGCCAAGAATAACTCTGGCTTCCGCCATGCCCCATGTCTCAGAAATAGGTGGC
CATGGGGCTTCACAAAATAATGAGATGCTCTGTGCAGTCTGAGAAAGCAAATTTGCCTCTTTTC
TTAACACAGTCTCTACTGGGGAAGCAGAACACTGGTGGGATAAAAACTTATCTAGAAGGGGAGA
AACTCCCTCCACTGTGAACAGTAAGCCAGAATATGCTTATTCCTCAGCATAAACAGTATCTCGG
AGAAGCCTGGGATGAGAAAATGAGGAGGATGGGTCCAAGAAACATGAGGCCTTCTTGACA

hide sequence

RefSeq Acc Id:

XM_047431660 ⟹ XP_047287616

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431661 ⟹ XP_047287617

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431662 ⟹ XP_047287618

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431663 ⟹ XP_047287619

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431664 ⟹ XP_047287620

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431665 ⟹ XP_047287621

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431666 ⟹ XP_047287622

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431667 ⟹ XP_047287623

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431668 ⟹ XP_047287624

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431669 ⟹ XP_047287625

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431671 ⟹ XP_047287627

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_047431672 ⟹ XP_047287628

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	22,985,894 - 23,010,143 (-)	NCBI

RefSeq Acc Id:

XM_054376543 ⟹ XP_054232518

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

RefSeq Acc Id:

XM_054376544 ⟹ XP_054232519

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

RefSeq Acc Id:

XM_054376545 ⟹ XP_054232520

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

RefSeq Acc Id:

XM_054376546 ⟹ XP_054232521

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

RefSeq Acc Id:

XM_054376547 ⟹ XP_054232522

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	17,186,512 - 17,201,655 (-)	NCBI

RefSeq Acc Id:

XM_054376548 ⟹ XP_054232523

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

RefSeq Acc Id:

XM_054376549 ⟹ XP_054232524

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

RefSeq Acc Id:

XM_054376550 ⟹ XP_054232525

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

RefSeq Acc Id:

XM_054376551 ⟹ XP_054232526

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	17,186,512 - 17,210,763 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001124178	(Get FASTA)	NCBI Sequence Viewer
	NP_001124180	(Get FASTA)	NCBI Sequence Viewer
	NP_001269897	(Get FASTA)	NCBI Sequence Viewer
	NP_001269898	(Get FASTA)	NCBI Sequence Viewer
	NP_001269899	(Get FASTA)	NCBI Sequence Viewer
	NP_068763	(Get FASTA)	NCBI Sequence Viewer
	XP_005268028	(Get FASTA)	NCBI Sequence Viewer
	XP_005268029	(Get FASTA)	NCBI Sequence Viewer
	XP_006720294	(Get FASTA)	NCBI Sequence Viewer
	XP_006720295	(Get FASTA)	NCBI Sequence Viewer
	XP_011535361	(Get FASTA)	NCBI Sequence Viewer
	XP_011535362	(Get FASTA)	NCBI Sequence Viewer
	XP_011535364	(Get FASTA)	NCBI Sequence Viewer
	XP_016877059	(Get FASTA)	NCBI Sequence Viewer
	XP_016877061	(Get FASTA)	NCBI Sequence Viewer
	XP_016877062	(Get FASTA)	NCBI Sequence Viewer
	XP_016877063	(Get FASTA)	NCBI Sequence Viewer
	XP_016877064	(Get FASTA)	NCBI Sequence Viewer
	XP_016877065	(Get FASTA)	NCBI Sequence Viewer
	XP_047287616	(Get FASTA)	NCBI Sequence Viewer
	XP_047287617	(Get FASTA)	NCBI Sequence Viewer
	XP_047287618	(Get FASTA)	NCBI Sequence Viewer
	XP_047287619	(Get FASTA)	NCBI Sequence Viewer
	XP_047287620	(Get FASTA)	NCBI Sequence Viewer
	XP_047287621	(Get FASTA)	NCBI Sequence Viewer
	XP_047287622	(Get FASTA)	NCBI Sequence Viewer
	XP_047287623	(Get FASTA)	NCBI Sequence Viewer
	XP_047287624	(Get FASTA)	NCBI Sequence Viewer
	XP_047287625	(Get FASTA)	NCBI Sequence Viewer
	XP_047287627	(Get FASTA)	NCBI Sequence Viewer
	XP_047287628	(Get FASTA)	NCBI Sequence Viewer
	XP_054232518	(Get FASTA)	NCBI Sequence Viewer
	XP_054232519	(Get FASTA)	NCBI Sequence Viewer
	XP_054232520	(Get FASTA)	NCBI Sequence Viewer
	XP_054232521	(Get FASTA)	NCBI Sequence Viewer
	XP_054232522	(Get FASTA)	NCBI Sequence Viewer
	XP_054232523	(Get FASTA)	NCBI Sequence Viewer
	XP_054232524	(Get FASTA)	NCBI Sequence Viewer
	XP_054232525	(Get FASTA)	NCBI Sequence Viewer
	XP_054232526	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH14299	(Get FASTA)	NCBI Sequence Viewer
	BAB13988	(Get FASTA)	NCBI Sequence Viewer
	BAB14363	(Get FASTA)	NCBI Sequence Viewer
	CAD61874	(Get FASTA)	NCBI Sequence Viewer
	CAD61892	(Get FASTA)	NCBI Sequence Viewer
	CAD61930	(Get FASTA)	NCBI Sequence Viewer
	CAD61946	(Get FASTA)	NCBI Sequence Viewer
	CAE90777	(Get FASTA)	NCBI Sequence Viewer
	EAW66196	(Get FASTA)	NCBI Sequence Viewer
	EAW66197	(Get FASTA)	NCBI Sequence Viewer
	EAW66198	(Get FASTA)	NCBI Sequence Viewer
	EAW66199	(Get FASTA)	NCBI Sequence Viewer
	EAW66200	(Get FASTA)	NCBI Sequence Viewer
	EAW66201	(Get FASTA)	NCBI Sequence Viewer
	EAW66202	(Get FASTA)	NCBI Sequence Viewer
	EAW66203	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000299088
	ENSP00000299088.6
	ENSP00000341353
	ENSP00000341353.4
	ENSP00000380532.2
	ENSP00000380533
	ENSP00000380533.1
	ENSP00000380535
	ENSP00000380535.3
	ENSP00000380536.2
	ENSP00000380538
	ENSP00000380538.4
	ENSP00000450771.1
	ENSP00000450866.1
	ENSP00000451111.1
	ENSP00000451155.1
	ENSP00000451456.1
	ENSP00000451762.1
	ENSP00000451879.1
	ENSP00000452036.1
	ENSP00000452088.1
GenBank Protein	Q9H972	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_068763 ⟸ NM_021944
- Peptide Label:	isoform a precursor
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	NP_001124178 ⟸ NM_001130706
- Peptide Label:	isoform a precursor
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	NP_001124180 ⟸ NM_001130708
- Peptide Label:	isoform a precursor
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_005268029 ⟸ XM_005267972
- Peptide Label:	isoform X1
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_005268028 ⟸ XM_005267971
- Peptide Label:	isoform X1
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	NP_001269897 ⟸ NM_001282968
- Peptide Label:	isoform b
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRLPGCTLAASEAAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGT KLPPPRPEDMLNAAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKL VHNVHNHITNDKRFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKR REYRNSLNPFKGLKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNE PGVWVARPPRFRAQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEE EDEGGDENAPGSPSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	NP_001269899 ⟸ NM_001282970
- Peptide Label:	isoform c
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPDRLPSAEAQLL PPELYNPNFQEEEDEGGDENAPGSPSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	NP_001269898 ⟸ NM_001282969
- Peptide Label:	isoform b
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRLPGCTLAASEAAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGT KLPPPRPEDMLNAAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKL VHNVHNHITNDKRFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKR REYRNSLNPFKGLKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNE PGVWVARPPRFRAQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEE EDEGGDENAPGSPSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_006720295 ⟸ XM_006720232
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRLPGCTLAASEAAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGT KLPPPRPEDMLNAAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKL VHNVHNHITNDKRFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKR REYRNSLNPFKGLKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNE PGVWVARPPRFRAQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEE EDEGGDENAPGSPSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_006720294 ⟸ XM_006720231
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRLPGCTLAASEAAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGT KLPPPRPEDMLNAAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKL VHNVHNHITNDKRFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKR REYRNSLNPFKGLKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNE PGVWVARPPRFRAQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEE EDEGGDENAPGSPSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_011535361 ⟸ XM_011537059
- Peptide Label:	isoform X1
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_011535364 ⟸ XM_011537062
- Peptide Label:	isoform X1
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_011535362 ⟸ XM_011537060
- Peptide Label:	isoform X1
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_016877065 ⟸ XM_017021576
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRLPGCTLAASEAAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGT KLPPPRPEDMLNAAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKL VHNVHNHITNDKRFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKR REYRNSLNPFKGLKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNE PGVWVARPPRFRAQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEE EDEGGDENAPGSPSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_016877062 ⟸ XM_017021573
- Peptide Label:	isoform X1
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_016877061 ⟸ XM_017021572
- Peptide Label:	isoform X1
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_016877059 ⟸ XM_017021570
- Peptide Label:	isoform X1
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_016877063 ⟸ XM_017021574
- Peptide Label:	isoform X1
- UniProtKB:	Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot), Q9H972 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSFSATILFSPPSGSEARCCCCACKSETNGGNTGSQGGNPPPSTPITVTGHGLAVQSSEQLLHV IYQRVDKAVGLAEAALGLARANNELLKRLQEEVGDLRQGKVSIPDEDGESRAHSSPPEEPGPLK ESPGEAFKALSAVEEECDSVGSGVQVVIEELRQLGAASVGPGPLGFPATQRDMRLPGCTLAASE AAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGTKLPPPRPEDMLN AAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKLVHNVHNHITNDK RFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKRREYRNSLNPFKG LKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNEPGVWVARPPRFR AQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEEEDEGGDENAPGS PSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:	XP_016877064 ⟸ XM_017021575
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRLPGCTLAASEAAPLLNPLVDDYVASEGAVQRVLVPAYAKQLSPATQLAIQRATPETGPENGT KLPPPRPEDMLNAAAALDSALEESGPGSTGELRHSLGLTVSPCRTRGSGQKNSRRKRDLVLSKL VHNVHNHITNDKRFNGSESIKSSWNISVVKFLLEKLKQELVTSPHNYTDKELKGACVAYFLTKR REYRNSLNPFKGLKEKEEKKLRSRRYRLFANRSSIMRHFGPEDQRLWNDVTEELMSDEEDSLNE PGVWVARPPRFRAQRLTELCYHLDANSKHGTKANRVYGPPSDRLPSAEAQLLPPELYNPNFQEE EDEGGDENAPGSPSFDQPHKTCCPDLNSFIEIKVEKDE hide sequence

RefSeq Acc Id:

ENSP00000451879 ⟸ ENST00000555998

RefSeq Acc Id:

ENSP00000450866 ⟸ ENST00000555098

RefSeq Acc Id:

ENSP00000451111 ⟸ ENST00000555575

RefSeq Acc Id:

ENSP00000451762 ⟸ ENST00000556419

RefSeq Acc Id:

ENSP00000299088 ⟸ ENST00000299088

RefSeq Acc Id:

ENSP00000341353 ⟸ ENST00000341470

RefSeq Acc Id:

ENSP00000450771 ⟸ ENST00000553675

RefSeq Acc Id:

ENSP00000451155 ⟸ ENST00000553606

RefSeq Acc Id:

ENSP00000451456 ⟸ ENST00000553958

RefSeq Acc Id:

ENSP00000452036 ⟸ ENST00000553931

RefSeq Acc Id:

ENSP00000380535 ⟸ ENST00000397379

RefSeq Acc Id:

ENSP00000380533 ⟸ ENST00000397377

RefSeq Acc Id:

ENSP00000380532 ⟸ ENST00000397376

RefSeq Acc Id:

ENSP00000380538 ⟸ ENST00000397382

RefSeq Acc Id:

ENSP00000380536 ⟸ ENST00000397380

RefSeq Acc Id:

ENSP00000452088 ⟸ ENST00000554179

RefSeq Acc Id:	XP_047287628 ⟸ XM_047431672
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047287619 ⟸ XM_047431663
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287627 ⟸ XM_047431671
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047287621 ⟸ XM_047431665
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287625 ⟸ XM_047431669
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047287622 ⟸ XM_047431666
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287618 ⟸ XM_047431662
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287616 ⟸ XM_047431660
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287620 ⟸ XM_047431664
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047287624 ⟸ XM_047431668
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047287623 ⟸ XM_047431667
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047287617 ⟸ XM_047431661
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054232525 ⟸ XM_054376550
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054232520 ⟸ XM_054376545
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054232523 ⟸ XM_054376548
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054232519 ⟸ XM_054376544
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054232526 ⟸ XM_054376551
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054232518 ⟸ XM_054376543
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054232524 ⟸ XM_054376549
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054232521 ⟸ XM_054376546
- Peptide Label:	isoform X1
- UniProtKB:	Q9H972 (UniProtKB/Swiss-Prot), Q96CF7 (UniProtKB/Swiss-Prot), Q86SE6 (UniProtKB/Swiss-Prot), D3DS39 (UniProtKB/Swiss-Prot), D3DS38 (UniProtKB/Swiss-Prot), B7WP03 (UniProtKB/Swiss-Prot), Q9HA68 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054232522 ⟸ XM_054376547
- Peptide Label:	isoform X2
- UniProtKB:	A0A0C4DFZ6 (UniProtKB/TrEMBL)

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9H972-F1-model_v2	AlphaFold	Q9H972	1-538	view protein structure

Promoters

RGD ID:

6810573

Promoter ID:

HG_ACW:22043

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:

C14ORF93.HAPR07, C14ORF93.JAPR07-UNSPLICED

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	14	22,545,871 - 22,546,371 (-)	MPROMDB

RGD ID:

6791456

Promoter ID:

HG_KWN:18984

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000397380, ENST00000406429, NM_001130706, NM_001130708, OTTHUMT00000071688, UC001WIA.2, UC001WID.1, UC001WIF.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	14	22,549,001 - 22,549,501 (-)	MPROMDB

RGD ID:

7227093

Promoter ID:

EPDNEW_H19292

Type:

multiple initiation site

Name:

C14orf93_1

Description:

chromosome 14 open reading frame 93

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	23,010,143 - 23,010,203	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:20162	AgrOrtholog
COSMIC	C14orf93	COSMIC
Ensembl Genes	ENSG00000100802	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000299088	ENTREZGENE
	ENST00000299088.11	UniProtKB/Swiss-Prot
	ENST00000341470	ENTREZGENE
	ENST00000341470.8	UniProtKB/Swiss-Prot
	ENST00000397376.6	UniProtKB/TrEMBL
	ENST00000397377	ENTREZGENE
	ENST00000397377.5	UniProtKB/TrEMBL
	ENST00000397379	ENTREZGENE
	ENST00000397379.7	UniProtKB/Swiss-Prot
	ENST00000397380.6	UniProtKB/TrEMBL
	ENST00000397382	ENTREZGENE
	ENST00000397382.8	UniProtKB/Swiss-Prot
	ENST00000553606.5	UniProtKB/TrEMBL
	ENST00000553675.5	UniProtKB/TrEMBL
	ENST00000553931.5	UniProtKB/TrEMBL
	ENST00000553958.5	UniProtKB/TrEMBL
	ENST00000554179.5	UniProtKB/TrEMBL
	ENST00000555098.5	UniProtKB/TrEMBL
	ENST00000555575.5	UniProtKB/TrEMBL
	ENST00000555998.5	UniProtKB/TrEMBL
	ENST00000556419.5	UniProtKB/TrEMBL
GTEx	ENSG00000100802	GTEx
HGNC ID	HGNC:20162	ENTREZGENE
Human Proteome Map	C14orf93	Human Proteome Map
InterPro	DUF4616	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:60686	UniProtKB/Swiss-Prot
NCBI Gene	60686	ENTREZGENE
PANTHER	PTHR14375	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SIMILAR TO RIKEN CDNA 4931414P19	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	DUF4616	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134982493	PharmGKB
UniProt	A0A0C4DFZ6	ENTREZGENE, UniProtKB/TrEMBL
	A0A0G2JL88_HUMAN	UniProtKB/TrEMBL
	B7WP03	ENTREZGENE
	CN093_HUMAN	UniProtKB/Swiss-Prot
	D3DS38	ENTREZGENE
	D3DS39	ENTREZGENE
	G3V2P0_HUMAN	UniProtKB/TrEMBL
	G3V2U2_HUMAN	UniProtKB/TrEMBL
	G3V396_HUMAN	UniProtKB/TrEMBL
	G3V3W0_HUMAN	UniProtKB/TrEMBL
	G3V4F1_HUMAN	UniProtKB/TrEMBL
	G3V4L9_HUMAN	UniProtKB/TrEMBL
	G3V4W6_HUMAN	UniProtKB/TrEMBL
	G5E9D9_HUMAN	UniProtKB/TrEMBL
	J3KPV9_HUMAN	UniProtKB/TrEMBL
	Q86SE6	ENTREZGENE
	Q96CF7	ENTREZGENE
	Q9H972	ENTREZGENE
	Q9HA68	ENTREZGENE
UniProt Secondary	B7WP03	UniProtKB/Swiss-Prot
	D3DS38	UniProtKB/Swiss-Prot
	D3DS39	UniProtKB/Swiss-Prot
	Q86SE6	UniProtKB/Swiss-Prot
	Q96CF7	UniProtKB/Swiss-Prot
	Q9HA68	UniProtKB/Swiss-Prot

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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Imported Disease Annotations - ClinVar