ZNF415 (zinc finger protein 415) - Rat Genome Database

Name: ZNF415
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: ZNF415 (zinc finger protein 415) Homo sapiens

Analyze

Symbol:

ZNF415

Name:

zinc finger protein 415

RGD ID:

1350513

HGNC Page

HGNC:20636

Description:

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in fibrillar center and microtubule cytoskeleton.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ11191; Pact; ZfLp

RGD Orthologs

Bonobo

Green Monkey

Alliance Genes

More Info

more info ...

Related Pseudogenes:

LOC100419845 ZNF415P1

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	19	53,107,879 - 53,132,910 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	53,107,879 - 53,133,077 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	53,611,132 - 53,636,163 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	58,302,944 - 58,327,957 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	58,302,944 - 58,327,957	NCBI
Celera	19	50,658,663 - 50,683,384 (-)	NCBI		Celera
Cytogenetic Map	19	q13.42	NCBI
HuRef	19	49,935,622 - 49,960,144 (-)	NCBI		HuRef
CHM1_1	19	53,612,901 - 53,637,963 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

4,4'-sulfonyldiphenol (EXP)

5-aza-2'-deoxycytidine (EXP)

aflatoxin B1 (EXP)

Aflatoxin B2 alpha (EXP)

arsenite(3-) (EXP)

atrazine (EXP)

avobenzone (EXP)

benzo[a]pyrene (EXP)

CGP 52608 (EXP)

cyclosporin A (EXP)

dioxygen (EXP)

dorsomorphin (EXP)

doxorubicin (EXP)

leflunomide (EXP)

nickel atom (EXP)

paracetamol (EXP)

SB 431542 (EXP)

trichostatin A (EXP)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

regulation of DNA-templated transcription (IEA)

regulation of transcription by RNA polymerase II (IBA,IEA)

Cellular Component

cytoplasm (IEA)

fibrillar center (IDA)

microtubule cytoskeleton (IDA)

nucleus (IBA,IEA)

Molecular Function

DNA binding (IEA)

DNA-binding transcription factor activity, RNA polymerase II-specific (IBA,IEA)

metal ion binding (IEA)

protein binding (IPI)

RNA polymerase II cis-regulatory region sequence-specific DNA binding (IBA,IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:8619474	PMID:8889549	PMID:9110174	PMID:12477932	PMID:14702039	PMID:15146197	PMID:16344560	PMID:17055453	PMID:17207965	PMID:18029348	PMID:21873635	PMID:22863851
PMID:25416956	PMID:29987050	PMID:31478661	PMID:31586073	PMID:32296183	PMID:32694731	PMID:36528617

Genomics

Comparative Map Data

ZNF415
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	53,107,879 - 53,133,077 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	53,611,132 - 53,636,163 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	58,302,944 - 58,327,957 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	58,302,944 - 58,327,957	NCBI
Celera	19	50,658,663 - 50,683,384 (-)	NCBI		Celera
Cytogenetic Map	19	q13.42	NCBI
HuRef	19	49,935,622 - 49,960,144 (-)	NCBI		HuRef
CHM1_1	19	53,612,901 - 53,637,963 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI		T2T-CHM13v2.0

ZNF415
(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	20	59,137,545 - 59,162,014 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	61,055,934 - 61,080,429 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	50,030,677 - 50,055,166 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	58,902,930 - 58,927,004 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	19	58,902,930 - 58,927,002 (-)	Ensembl	panpan1.1		panPan2

ZNF415
(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	6	45,849,447 - 45,871,767 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	6	45,847,493 - 45,857,594 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666073	25,953,024 - 25,977,254 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants

Variants in ZNF415
32 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	copy number gain	See cases [RCV000050883]	Chr19:50191219..58535818 [GRCh38] Chr19:50694476..59047185 [GRCh37] Chr19:55386288..63738997 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.41-13.42(chr19:52707235-53192628)x1	copy number loss	See cases [RCV000052096]	Chr19:52707235..53192628 [GRCh38] Chr19:53210488..53695881 [GRCh37] Chr19:57902300..58387693 [NCBI36] Chr19:19q13.41-13.42	uncertain significance
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	copy number gain	See cases [RCV000052925]	Chr19:49907832..58557889 [GRCh38] Chr19:50411089..59069256 [GRCh37] Chr19:55102901..63761068 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	copy number gain	See cases [RCV000052926]	Chr19:51141518..58539965 [GRCh38] Chr19:51644775..59051332 [GRCh37] Chr19:56336587..63743144 [NCBI36] Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	copy number gain	See cases [RCV000052914]	Chr19:47908540..58539965 [GRCh38] Chr19:48411797..59051332 [GRCh37] Chr19:53103609..63743144 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	copy number gain	See cases [RCV000052915]	Chr19:47929575..58572206 [GRCh38] Chr19:48432832..59083573 [GRCh37] Chr19:53124644..63775385 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3	copy number gain	See cases [RCV000134174]	Chr19:52612432..58581203 [GRCh38] Chr19:53115685..59092570 [GRCh37] Chr19:57807497..63784382 [NCBI36] Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3	copy number gain	See cases [RCV000134139]	Chr19:52955056..58581203 [GRCh38] Chr19:53458309..59092570 [GRCh37] Chr19:58150121..63784382 [NCBI36] Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	copy number gain	See cases [RCV000135843]	Chr19:50152520..58581203 [GRCh38] Chr19:50655777..59092570 [GRCh37] Chr19:55347589..63784382 [NCBI36] Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3	copy number gain	See cases [RCV000142008]	Chr19:52143873..58445521 [GRCh38] Chr19:52647126..58956888 [GRCh37] Chr19:57338938..63648700 [NCBI36] Chr19:19q13.41-13.43	pathogenic
GRCh37/hg19 19q13.42(chr19:53600845-53630543)x1	copy number loss	not provided [RCV000752758]	Chr19:53600845..53630543 [GRCh37] Chr19:19q13.42	benign
GRCh37/hg19 19q13.42(chr19:53601649-53627882)x1	copy number loss	not provided [RCV000752759]	Chr19:53601649..53627882 [GRCh37] Chr19:19q13.42	benign
GRCh37/hg19 19q13.42(chr19:53627777-53631739)x0	copy number loss	not provided [RCV000752760]	Chr19:53627777..53631739 [GRCh37] Chr19:19q13.42	benign
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	copy number gain	See cases [RCV000445925]	Chr19:50489390..59095359 [GRCh37] Chr19:19q13.33-13.43	pathogenic
GRCh37/hg19 19q13.42(chr19:53606604-53636067)x3	copy number gain	See cases [RCV000448959]	Chr19:53606604..53636067 [GRCh37] Chr19:19q13.42	benign
NM_018355.4(ZNF415):c.1129A>G (p.Ile377Val)	single nucleotide variant	Inborn genetic diseases [RCV003277603]	Chr19:53108916 [GRCh38] Chr19:53612169 [GRCh37] Chr19:19q13.42	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	copy number gain	See cases [RCV000511289]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic\|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	copy number gain	See cases [RCV000512296]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19q13.42(chr19:53629589-53630478)x1	copy number loss	not provided [RCV000752761]	Chr19:53629589..53630478 [GRCh37] Chr19:19q13.42	benign
GRCh37/hg19 19q13.42(chr19:53630478-53632189)x0	copy number loss	not provided [RCV000752762]	Chr19:53630478..53632189 [GRCh37] Chr19:19q13.42	benign
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3	copy number gain	not provided [RCV000752444]	Chr19:260912..59097160 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3	copy number gain	not provided [RCV000752439]	Chr19:68029..59110290 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19q13.41-13.42(chr19:53184204-54346718)x3	copy number gain	not provided [RCV000740221]	Chr19:53184204..54346718 [GRCh37] Chr19:19q13.41-13.42	uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:50740074-59097160)x3	copy number gain	not provided [RCV000740208]	Chr19:50740074..59097160 [GRCh37] Chr19:19q13.33-13.43	pathogenic
NM_018355.4(ZNF415):c.287T>G (p.Phe96Cys)	single nucleotide variant	Inborn genetic diseases [RCV003244527]	Chr19:53109758 [GRCh38] Chr19:53613011 [GRCh37] Chr19:19q13.42	uncertain significance
GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871)	copy number gain	not provided [RCV001249294]	Chr19:47939842..54626871 [GRCh37] Chr19:19q13.32-13.42	not provided
GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3	copy number gain	not provided [RCV001007050]	Chr19:44738088..53621561 [GRCh37] Chr19:19q13.31-13.42	pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3	copy number gain	not provided [RCV001259944]	Chr19:48463931..57095254 [GRCh37] Chr19:19q13.33-13.43	pathogenic
NM_018355.4(ZNF415):c.373C>A (p.Arg125Ser)	single nucleotide variant	Inborn genetic diseases [RCV003285989]	Chr19:53109672 [GRCh38] Chr19:53612925 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.872G>A (p.Arg291Gln)	single nucleotide variant	Inborn genetic diseases [RCV002990604]	Chr19:53109173 [GRCh38] Chr19:53612426 [GRCh37] Chr19:19q13.42	likely benign
NM_018355.4(ZNF415):c.15+248A>T	single nucleotide variant	Inborn genetic diseases [RCV002684271]	Chr19:53122414 [GRCh38] Chr19:53625667 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.367G>T (p.Asp123Tyr)	single nucleotide variant	Inborn genetic diseases [RCV002687195]	Chr19:53109678 [GRCh38] Chr19:53612931 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1096A>G (p.Ser366Gly)	single nucleotide variant	Inborn genetic diseases [RCV003000262]	Chr19:53108949 [GRCh38] Chr19:53612202 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.40G>A (p.Glu14Lys)	single nucleotide variant	Inborn genetic diseases [RCV003000692]	Chr19:53116409 [GRCh38] Chr19:53619662 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1072T>C (p.Cys358Arg)	single nucleotide variant	Inborn genetic diseases [RCV002762138]	Chr19:53108973 [GRCh38] Chr19:53612226 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.847C>T (p.Arg283Cys)	single nucleotide variant	Inborn genetic diseases [RCV002782943]	Chr19:53109198 [GRCh38] Chr19:53612451 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1322A>G (p.Lys441Arg)	single nucleotide variant	Inborn genetic diseases [RCV002757798]	Chr19:53108723 [GRCh38] Chr19:53611976 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1250G>A (p.Cys417Tyr)	single nucleotide variant	Inborn genetic diseases [RCV002759961]	Chr19:53108795 [GRCh38] Chr19:53612048 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1606C>T (p.Arg536Cys)	single nucleotide variant	Inborn genetic diseases [RCV002978601]	Chr19:53108439 [GRCh38] Chr19:53611692 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1147C>A (p.Pro383Thr)	single nucleotide variant	Inborn genetic diseases [RCV002739390]	Chr19:53108898 [GRCh38] Chr19:53612151 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1208G>C (p.Trp403Ser)	single nucleotide variant	Inborn genetic diseases [RCV002886860]	Chr19:53108837 [GRCh38] Chr19:53612090 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1658A>G (p.Lys553Arg)	single nucleotide variant	Inborn genetic diseases [RCV002804866]	Chr19:53108387 [GRCh38] Chr19:53611640 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1332G>C (p.Glu444Asp)	single nucleotide variant	Inborn genetic diseases [RCV002709593]	Chr19:53108713 [GRCh38] Chr19:53611966 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.139C>A (p.Leu47Met)	single nucleotide variant	Inborn genetic diseases [RCV002743066]	Chr19:53109906 [GRCh38] Chr19:53613159 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1311G>T (p.Glu437Asp)	single nucleotide variant	Inborn genetic diseases [RCV002897499]	Chr19:53108734 [GRCh38] Chr19:53611987 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.960A>C (p.Lys320Asn)	single nucleotide variant	Inborn genetic diseases [RCV002832454]	Chr19:53109085 [GRCh38] Chr19:53612338 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1552C>T (p.His518Tyr)	single nucleotide variant	Inborn genetic diseases [RCV002746860]	Chr19:53108493 [GRCh38] Chr19:53611746 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.754G>A (p.Val252Ile)	single nucleotide variant	Inborn genetic diseases [RCV002725235]	Chr19:53109291 [GRCh38] Chr19:53612544 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1454C>T (p.Thr485Ile)	single nucleotide variant	Inborn genetic diseases [RCV002679786]	Chr19:53108591 [GRCh38] Chr19:53611844 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.986C>T (p.Thr329Ile)	single nucleotide variant	Inborn genetic diseases [RCV003178035]	Chr19:53109059 [GRCh38] Chr19:53612312 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1630A>G (p.Ile544Val)	single nucleotide variant	Inborn genetic diseases [RCV003192014]	Chr19:53108415 [GRCh38] Chr19:53611668 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1301A>G (p.His434Arg)	single nucleotide variant	Inborn genetic diseases [RCV003189339]	Chr19:53108744 [GRCh38] Chr19:53611997 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.329T>C (p.Val110Ala)	single nucleotide variant	Inborn genetic diseases [RCV003308892]	Chr19:53109716 [GRCh38] Chr19:53612969 [GRCh37] Chr19:19q13.42	likely benign
NM_018355.4(ZNF415):c.317A>G (p.Asn106Ser)	single nucleotide variant	Inborn genetic diseases [RCV003304520]	Chr19:53109728 [GRCh38] Chr19:53612981 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.1088A>G (p.Lys363Arg)	single nucleotide variant	Inborn genetic diseases [RCV003353711]	Chr19:53108957 [GRCh38] Chr19:53612210 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.125T>C (p.Leu42Pro)	single nucleotide variant	Inborn genetic diseases [RCV003373414]	Chr19:53116324 [GRCh38] Chr19:53619577 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.706G>T (p.Val236Leu)	single nucleotide variant	Inborn genetic diseases [RCV003369056]	Chr19:53109339 [GRCh38] Chr19:53612592 [GRCh37] Chr19:19q13.42	uncertain significance
NM_018355.4(ZNF415):c.31G>A (p.Val11Met)	single nucleotide variant	Inborn genetic diseases [RCV003354937]	Chr19:53116418 [GRCh38] Chr19:53619671 [GRCh37] Chr19:19q13.42	uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	copy number gain	not provided [RCV003485200]	Chr19:49625130..57647352 [GRCh37] Chr19:19q13.33-13.43	likely pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	6804
Count of miRNA genes:	898
Interacting mature miRNAs:	1059
Transcripts:	ENST00000243643, ENST00000421033, ENST00000440291, ENST00000448501, ENST00000455735, ENST00000500065, ENST00000594011, ENST00000594286, ENST00000595174, ENST00000595193, ENST00000595359, ENST00000595813, ENST00000596051, ENST00000596106, ENST00000596683, ENST00000597503, ENST00000597748, ENST00000597877, ENST00000598024, ENST00000598578, ENST00000599261, ENST00000600098, ENST00000600120, ENST00000600574, ENST00000601110, ENST00000601215, ENST00000601493, ENST00000602024, ENST00000602110
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

Markers in Region

D19S679E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	53,611,366 - 53,611,479	UniSTS	GRCh37
Build 36	19	58,303,178 - 58,303,291	RGD	NCBI36
Celera	19	50,658,897 - 50,659,010	RGD
Cytogenetic Map	19	q13.42	UniSTS
HuRef	19	49,935,856 - 49,935,969	UniSTS
GeneMap99-GB4 RH Map	19	278.55	UniSTS

SHGC-32227

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	53,611,133 - 53,611,282	UniSTS	GRCh37
Build 36	19	58,302,945 - 58,303,094	RGD	NCBI36
Celera	19	50,658,664 - 50,658,813	RGD
Cytogenetic Map	19	q13.42	UniSTS
HuRef	19	49,935,623 - 49,935,772	UniSTS
TNG Radiation Hybrid Map	19	21299.0	UniSTS
Stanford-G3 RH Map	19	2725.0	UniSTS
GeneMap99-GB4 RH Map	19	308.56	UniSTS
Whitehead-RH Map	19	383.1	UniSTS
NCBI RH Map	19	574.7	UniSTS
GeneMap99-G3 RH Map	19	2736.0	UniSTS

G20866

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	53,612,024 - 53,612,129	UniSTS	GRCh37
Build 36	19	58,303,836 - 58,303,941	RGD	NCBI36
Celera	19	50,659,555 - 50,659,660	RGD
Cytogenetic Map	19	q13.42	UniSTS
HuRef	19	49,936,514 - 49,936,619	UniSTS

A006J12

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	53,612,024 - 53,612,129	UniSTS	GRCh37
GRCh37	19	53,611,520 - 53,612,129	UniSTS	GRCh37
Build 36	19	58,303,836 - 58,303,941	RGD	NCBI36
Celera	19	50,659,051 - 50,659,660	UniSTS
Celera	19	50,659,555 - 50,659,660	RGD
Cytogenetic Map	19	q13.42	UniSTS
HuRef	19	49,936,010 - 49,936,619	UniSTS
HuRef	19	49,936,514 - 49,936,619	UniSTS
GeneMap99-GB4 RH Map	19	278.34	UniSTS
NCBI RH Map	19	576.1	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

187

623

154

1167

771

464

Low

2143

2209

902

416

914

256

4117

2077

2550

335

634

1076

165

1164

2679

Below cutoff

694

193

896

193

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001136038	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001164309	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001330759	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001330766	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352130	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352131	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352132	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352133	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352134	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352135	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352136	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352137	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352138	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352139	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352140	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352141	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352142	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352143	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352144	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352146	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352147	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352148	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352149	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352150	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352151	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_018355	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006723267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006723279	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006723280	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011527101	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026956	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026957	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026960	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026961	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026964	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026968	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026969	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026970	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017026971	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451595	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451596	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451597	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451598	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451599	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451600	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451601	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439079	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439080	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439081	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439082	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439083	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439084	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439085	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439086	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439087	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439088	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439089	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439090	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439091	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321419	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321420	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321421	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321422	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321423	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321424	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321425	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321426	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321427	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321428	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321429	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321430	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321431	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321432	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321433	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321434	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321435	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321436	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054321437	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA125787	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB480247	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC010328	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF038179	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK002053	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK095504	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL534796	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY283600	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC063880	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC069668	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471135	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN426971	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA075573	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA099143	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA348212	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA367299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA505759	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA518713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA692431	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA767859	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB026064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB052912	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB173728	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB223753	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB285275	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DQ925695	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DQ925696	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DQ925697	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DQ925698	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EL736353	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KT585023	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	R40095	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000243643 ⟹ ENSP00000243643

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,107,879 - 53,132,910 (-)	Ensembl

RefSeq Acc Id:

ENST00000421033 ⟹ ENSP00000395055

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,107,880 - 53,132,918 (-)	Ensembl

RefSeq Acc Id:

ENST00000500065 ⟹ ENSP00000439435

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,107,883 - 53,132,888 (-)	Ensembl

RefSeq Acc Id:

ENST00000594011 ⟹ ENSP00000472584

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,107,880 - 53,132,892 (-)	Ensembl

RefSeq Acc Id:

ENST00000594286

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,115,784 - 53,132,920 (-)	Ensembl

RefSeq Acc Id:

ENST00000595174 ⟹ ENSP00000471386

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,109,692 - 53,129,709 (-)	Ensembl

RefSeq Acc Id:

ENST00000595193 ⟹ ENSP00000472516

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,107,879 - 53,132,895 (-)	Ensembl

RefSeq Acc Id:

ENST00000595359

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,109,738 - 53,133,077 (-)	Ensembl

RefSeq Acc Id:

ENST00000595813 ⟹ ENSP00000470272

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,109,806 - 53,132,900 (-)	Ensembl

RefSeq Acc Id:

ENST00000596051 ⟹ ENSP00000473008

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,116,379 - 53,132,900 (-)	Ensembl

RefSeq Acc Id:

ENST00000596106

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,115,757 - 53,132,900 (-)	Ensembl

RefSeq Acc Id:

ENST00000596683

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,115,734 - 53,132,892 (-)	Ensembl

RefSeq Acc Id:

ENST00000597503 ⟹ ENSP00000468917

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,107,879 - 53,132,886 (-)	Ensembl

RefSeq Acc Id:

ENST00000597748 ⟹ ENSP00000469656

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,107,898 - 53,123,649 (-)	Ensembl

RefSeq Acc Id:

ENST00000597877 ⟹ ENSP00000471718

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,115,847 - 53,129,699 (-)	Ensembl

RefSeq Acc Id:

ENST00000598024 ⟹ ENSP00000472003

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,115,235 - 53,132,904 (-)	Ensembl

RefSeq Acc Id:

ENST00000598578 ⟹ ENSP00000472673

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,108,101 - 53,132,881 (-)	Ensembl

RefSeq Acc Id:

ENST00000599261 ⟹ ENSP00000471167

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,109,877 - 53,132,884 (-)	Ensembl

RefSeq Acc Id:

ENST00000600098

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,116,260 - 53,132,916 (-)	Ensembl

RefSeq Acc Id:

ENST00000600120 ⟹ ENSP00000471834

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,107,879 - 53,132,875 (-)	Ensembl

RefSeq Acc Id:

ENST00000600574 ⟹ ENSP00000469483

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,116,105 - 53,132,900 (-)	Ensembl

RefSeq Acc Id:

ENST00000601110 ⟹ ENSP00000470410

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,109,727 - 53,132,904 (-)	Ensembl

RefSeq Acc Id:

ENST00000601215 ⟹ ENSP00000472797

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,109,672 - 53,129,665 (-)	Ensembl

RefSeq Acc Id:

ENST00000601493 ⟹ ENSP00000472911

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,107,879 - 53,132,875 (-)	Ensembl

RefSeq Acc Id:

ENST00000602024

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,109,607 - 53,132,904 (-)	Ensembl

RefSeq Acc Id:

ENST00000602110

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	53,115,258 - 53,132,900 (-)	Ensembl

RefSeq Acc Id:

NM_001136038 ⟹ NP_001129510

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
GRCh37	19	53,611,132 - 53,636,173 (-)	RGD
Celera	19	50,658,663 - 50,683,384 (-)	RGD
HuRef	19	49,935,622 - 49,960,144 (-)	ENTREZGENE
CHM1_1	19	53,612,901 - 53,637,961 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGGTGGGAGACAATGCCTTGGAGCTGCAAATC
TTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTCACATTGACCCGTGCCTTCCCTCAGT
CCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCCTGTGACATGAACTTCTGAAGAGTCC
ACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATGGATGGAGACGGGTTGACATTCAGGG
ACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTATA
CAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGATCTGTCTCGTAACTGTGTA
ATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGG
AACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGA
CTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAA
AATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATC
AGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAAT
TTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATA
ATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCAT
TACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAA
AGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATAT
AAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTC
ATACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCT
TGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTC
TTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACAT
GTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAG
TGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCA
ACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCA
GTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAA
TGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGA
GAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCC
ATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGT
GCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAG
TGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGA
AACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCA
AATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGT
TTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTG
GCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCC
TTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAA
AGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGAC
ATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAA
CTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCA
TATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATAT
TAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001164309 ⟹ NP_001157781

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
GRCh37	19	53,611,132 - 53,636,173 (-)	RGD
Celera	19	50,658,663 - 50,683,384 (-)	RGD
HuRef	19	49,935,622 - 49,960,144 (-)	ENTREZGENE
CHM1_1	19	53,612,901 - 53,637,961 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGCATTGACTTCCAAAGACTCCTGGCACATGA
GGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGG
GACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTAT
ACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGATCTGTCTCGTAACTGTGT
AATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTG
GAACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACG
ACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGA
AAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACAT
CAGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAA
TTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAAT
AATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCA
TTACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACA
AAGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATA
TAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTT
CATACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCC
TTGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGT
CTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACA
TGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATA
GTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGC
AACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTC
AGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCA
ATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGG
AGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACC
CATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTG
TGCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGA
GTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAG
AAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATC
AAATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAG
TTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGT
GGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATC
CTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTA
AAGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGA
CATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAA
ACTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTC
ATATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATA
TTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001330759 ⟹ NP_001317688

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGCATTGACTTCCAAAGACTCCTGGCACATGA
GGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGATCTGTCTCGTA
ACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGT
GACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAA
ATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCC
CAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTAT
TAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAA
GGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCAC
CCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTG
TTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAG
TGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGA
AAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTG
GAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAAC
TCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTG
ACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACC
TTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTA
ATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAA
GCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAA
AGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTAC
AAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTC
ATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTT
AACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGC
TTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAAT
GTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATAC
TGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTC
AGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCA
GTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAA
TAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGA
GAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTC
CATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACT
CACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAG
GATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAA
ACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATG
ATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001330766 ⟹ NP_001317695

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGACCTCTCT
GACCTCATCTCCTGCCTGTGTCCTCCTCGCTCCCTCTGCTCCAGCCAAGCATGCGTCCTTCCTG
TTCCTGGGCCGAGCTTGCTCCTGCCTCAAGGCCTTCACGTGGGCTGTGCCTCTGCTGGAACTCG
CTGGCCCCTCAGCTGCAGCATTGACTTCCAAAGACTCCTGGCACATGAGGAAGAAACCCAGAAG
AGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGGGACGTGGCCATCGAAT
TCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTATACAGGGATGTGATGTT
GGAGAACTACAGGAACCTGGTCTCCCTGGAGTATTATCCTATGTGGGAGCACAGGAAAGAGCCC
TGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAAGGGTGGGAATGGATCAAAGGTG
TGAAAACAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCA
AATGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAA
TCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGA
ACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGAC
TTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAA
ATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCA
GCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATT
TATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAA
TTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATT
ACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAA
GCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATA
AATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCA
TACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTT
GCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCT
TCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATG
TAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGT
GGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAA
CTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAG
TCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAAT
GAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAG
AGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCA
TCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTG
CATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGT
GTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAA
ACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAA
ATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTT
TAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGG
CAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCT
TACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAA
GAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACA
TCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAAC
TGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCAT
ATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATT
AAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352130 ⟹ NP_001339059

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGAAAGGTGGGAGACAATGCCTTGGAGCTGCA
AATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTCACATTGACCCGTGCCTTCCCT
CAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCCTGTGACATGAACTTCTGAAGA
GTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATGGATGGAGACGGGTTGACATTC
AGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTT
TATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGAGTATTATCCTATGTG
GGAGCACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAAGGG
TGGGAATGGATCAAAGGTGTGAAAACAGATGGAGTTTCGCTCTTATTGCCCAGGCTGGAGTGCA
ATGGTGCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTCCTGCCTCAGC
CTCCCGAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAA
CAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACA
TTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGA
TGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGAC
CAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTAC
CACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGA
GAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACC
CATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAAT
CATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACA
CATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAG
GTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACA
AATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCA
CACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTT
GCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCT
TTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATG
CAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACT
GGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAA
GGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAG
TTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAAT
GAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAG
AGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCA
TCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTG
CGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATT
GTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAA
ACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAA
AGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATT
CACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTT
CATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAA
CTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTT
TGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTT
ATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAA
TGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGA
AGTCA

hide sequence

RefSeq Acc Id:

NM_001352131 ⟹ NP_001339060

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGGGAGAC
AATGCCTTGGAGCTGCAAATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTCACAT
TGACCCGTGCCTTCCCTCAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCCTGTG
ACATGAACTTCTGAAGAGTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATGGATG
GAGACGGGTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAA
CTCTACACAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTG
GAGTATTATCCTATGTGGGAGCACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGAGTAG
CAAGAAAACCAAAAGGGTGGGAATGGATCAAAGGTGTGAAAACAGATGGAGTTTCGCTCTTATT
GCCCAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAAT
GATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCA
AGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACA
ACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTT
GACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATC
TTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCT
TGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTAT
GAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTT
CTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACT
CACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCC
TTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAAT
GTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATAC
TGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCA
CTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCA
GTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAA
AGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGC
AAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTC
ATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCA
GACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAA
TGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGA
AACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCA
GGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCAT
TCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTG
GCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACC
TTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATT
ATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAA
ATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAA
GGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTAC
GAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAG
AAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCA
AAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGT
AACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATT
ACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAA
GGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352132 ⟹ NP_001339061

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCAAAGGTGGG
AGACAATGCCTTGGAGCTGCAAATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTC
ACATTGACCCGTGCCTTCCCTCAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCC
TGTGACATGAACTTCTGAAGAGTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATG
GATGGAGACGGGTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCC
TGAACTCTACACAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTC
CCTGGAGTATTATCCTATGTGGGAGCACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGA
GTAGCAAGAAAACCAAAAGGGTGGGAATGGATCAAAGGTGTGAAAACAGGCTGGAGTGCAATGG
TGCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTCCTGCCTCAGCCTCC
CGAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGG
AAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGA
AGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGAT
GAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAAC
GCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACA
TCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAG
TCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATG
TTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATG
CATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATG
ACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCT
TTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATG
TAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACT
GGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCAC
TACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAG
TGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAAT
GAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGG
AGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCA
TTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTAC
AATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGT
GTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAA
GCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAG
GTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCC
CAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGG
GAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCT
TATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAA
TTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACT
CCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATC
ACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGT
GTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTA
TATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGT
GAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCA
AGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTC
A

hide sequence

RefSeq Acc Id:

NM_001352133 ⟹ NP_001339062

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGAAAGGTGGGAGACAATGCCTTGGAGCTGCA
AATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTCACATTGACCCGTGCCTTCCCT
CAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCCTGTGACATGAACTTCTGAAGA
GTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATGGATGGAGACGGGTTGACATTC
AGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTT
TATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGAGTATTATCCTATGTG
GGAGCACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAAGGG
TGGGAATGGATCAAAGGTGTGAAAACAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAA
CCTTCGCCTCCCGGATTCAAATGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGAT
CTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTAT
TCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAAT
CAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTG
ACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAA
ACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTT
TCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCA
GTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTG
ATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAG
ATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCAT
TCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTG
CGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTT
CAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGT
TATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTG
GAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAA
CCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGT
CAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATG
AATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGA
GAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCAT
CGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGC
ATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATG
TGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAA
CCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGA
TAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCC
AAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGC
AAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCAT
ACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATT
TCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGA
CATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGG
TCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCT
ATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTT
GTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTC
ACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352134 ⟹ NP_001339063

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGCATTGACTTCCAAAGACTCCTGGCACATGA
GGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGG
GACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTAT
ACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGAGTATTATCCTATGTGGGA
GCACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAAGGGTGG
GAATGGATCAAAGGTGTGAAAACAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCT
TCGCCTCCCGGATTCAAATGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGATCTG
TCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCC
ACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAA
GAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACT
ACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACA
AGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCA
AGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTT
TCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATT
TCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATA
TATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCT
GGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGC
GTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAG
TCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTAT
GAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAG
AGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCA
TCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAG
ACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAAT
GTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAA
ACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGG
AGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATT
CGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGG
CAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCT
TACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAA
TCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAA
CCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAG
GTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACA
AGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCA
TTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACAT
CAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCT
CACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATT
AACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTG
CTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACA
CAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352135 ⟹ NP_001339064

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,129,686 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,211,977 (-)	NCBI

Sequence:

show sequence

CTCACTCAACTCAGACCTCTCAGGATAACTTGGTGAAATGACTCCCTCTCTCAGCCTCAGTGAG
CCCACCTGTAACAGAGATAAGGGACTAGACCAGAAAACCTCAATCATTGACTTCCAAAGACTCC
TGGCACATGAGGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTT
GACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAG
AGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGATCTGTCTC
GTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACAC
AGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAA
AAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGG
CCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTC
TATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCT
GAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCAC
CACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCAT
CTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATT
GAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAG
AGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCA
TTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGC
AACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGT
GTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAA
ACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAG
GTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTT
CAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGG
TAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCT
TACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAG
TTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAA
CTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAA
GGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACA
AATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCA
TACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTC
TTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCT
TCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTA
TAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCT
TGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGA
GTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACA
ACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACC
AAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGA
TAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAAC
ATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352136 ⟹ NP_001339065

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCAAAGGTGGG
AGACAATGCCTTGGAGCTGCAAATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTC
ACATTGACCCGTGCCTTCCCTCAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCC
TGTGACATGAACTTCTGAAGAGTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATG
GATGGAGACGGGTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCC
TGAACTCTACACAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTC
CCTGGAGTATTATCCTATGTGGGAGCACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGA
GTAGCAAGAAAACCAAAAGGGTGGGAATGGATCAAAGGTGTGAAAACAGATCTGTCTCGTAACT
GTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGAC
ATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATA
CACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAA
AAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAA
ACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGG
AAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCC
AAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTC
TTCATTACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGC
GACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAG
GATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAG
AGTTCATACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCA
TGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACA
AGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTA
CACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATT
CATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCC
TTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGT
CTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAA
TGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATA
CTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAAC
TACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTC
AGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTA
ATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGG
AAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGA
CATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTC
AAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAA
ATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAG
AATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCAT
GCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCAC
TAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGAT
CAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACT
TTTCATATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATA
TATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352137 ⟹ NP_001339066

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGAAAGGTGGGAGACAATGCCTTGGAGCTGCA
AATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTCACATTGACCCGTGCCTTCCCT
CAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCCTGTGACATGAACTTCTGAAGA
GTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATGGATGGAGACGGGTTGACATTC
AGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTT
TATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGAGTATTATCCTATGTG
GGAGCACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAAGGG
TGGGAATGGATCAAAGGTGTGAAAACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCAC
CACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACA
TGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGG
AGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGA
GAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTT
TCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCAT
GTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCA
AAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACA
GAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGC
TCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTG
GCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACC
ATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGA
GTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCAT
GCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAA
AGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTAC
AAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTC
ACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCT
TGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTT
TTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGT
GTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATAC
TGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACT
ACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTA
GTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAG
TGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAG
GAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTC
ATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCA
CAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAA
CCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACA
CCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAAC
ATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAG
GATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGA
ACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATG
TTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352138 ⟹ NP_001339067

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCAAAGGTGGG
AGACAATGCCTTGGAGCTGCAAATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTC
ACATTGACCCGTGCCTTCCCTCAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCC
TGTGACATGAACTTCTGAAGAGTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATG
GATGGAGACGGGTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCC
TGAACTCTACACAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTC
CCTGGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATG
ATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAA
GGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAA
CATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTG
ACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCT
TACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTT
GGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATG
AATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTC
TTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTC
ACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCT
TGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATG
TGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACT
GGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCAC
TACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAG
TCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAA
GAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCA
AGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCA
TCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAG
ACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAAT
GTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAA
ACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAG
GTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATT
CAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGG
CAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCT
TACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTA
TCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAA
TCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAG
GTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACG
AGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGA
AATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAA
AATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTA
ACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTA
CACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAG
GTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352139 ⟹ NP_001339068

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCCATTGACTT
CCAAAGACTCCTGGCACATGAGGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCT
TTTACTCAGTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGA
ACTCTACACAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCT
GGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATT
CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGA
ACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACAT
GAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACT
GTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTAC
TTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGA
TTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAAT
GTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTC
TACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACA
CAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGA
ATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGA
TCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGA
GAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTAC
ATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCG
AAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAG
TGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGA
AACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCA
GAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACT
TCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTG
GTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACC
TTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTC
ATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAA
GCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAA
ATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTAC
AAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCC
ATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCC
TGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTT
TTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGT
ACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAAT
CATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAAT
GTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACA
CATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACAC
ATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTT
GCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352140 ⟹ NP_001339069

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGCATTGACTTCCAAAGACTCCTGGCACATGA
GGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGG
GACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTAT
ACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGGCTGGAGTGCAATGGTGCA
ATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTCCTGCCTCAGCCTCCCGAG
TAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGG
TAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAG
TTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAA
GAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGA
TAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCC
CATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTG
TCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTC
TAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATT
AGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTG
TACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAG
TCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAAT
GAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAG
AGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACA
TCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTG
AGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAAT
GTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAA
ACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGG
AGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATT
CACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGG
GAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCT
TACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCA
TCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAA
CCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAG
TCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATA
AAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTA
TATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTA
CACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAA
GTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGG
CAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATT
TTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGG
AATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCC
CAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352141 ⟹ NP_001339070

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGAAAGGTGGGAGACAATGCCTTGGAGCTGCA
AATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTCACATTGACCCGTGCCTTCCCT
CAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCCTGTGACATGAACTTCTGAAGA
GTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATGGATGGAGACGGGTTGACATTC
AGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTT
TATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGGCTGGAGTGCAATGGT
GCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTCCTGCCTCAGCCTCCC
GAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGA
AGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAA
GAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATG
AAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACG
CGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACAT
CCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGT
CTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGT
TTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGC
ATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGA
CTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTT
TAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGT
AATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTG
GAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACT
ACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGT
GTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATG
AATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGA
GAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCAT
TGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACA
ATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTG
TGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAG
CCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGG
TCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCC
AAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGG
AAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTT
ATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAAT
TTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTC
CTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCA
CAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTG
TGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTAT
ATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTG
AGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAA
GCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352142 ⟹ NP_001339071

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCAAAGGTGGG
AGACAATGCCTTGGAGCTGCAAATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTC
ACATTGACCCGTGCCTTCCCTCAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCC
TGTGACATGAACTTCTGAAGAGTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATG
GATGGAGACGGGTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCC
TGAACTCTACACAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTC
CCTGGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGA
GAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCA
GGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAA
CAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGT
ATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGC
AGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGG
TTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATAT
GGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGGAAAAAC
CTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGT
AAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCA
AACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAATGTGACA
GAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTA
CAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACT
CATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACAC
TTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGT
GTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAG
TGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATA
CTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGC
GAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTT
AGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTA
ATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGG
AGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGA
CATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTG
TGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTA
ATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAG
AAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCA
GAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCAT
TCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTC
ATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGT
TGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAG
TCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAATATGTT
AAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352143 ⟹ NP_001339072

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGAAAGGTGGGAGACAATGCCTTGGAGCTGCA
AATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTCACATTGACCCGTGCCTTCCCT
CAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCCTGTGACATGAACTTCTGAAGA
GTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATGGATGGAGACGGGTTGACATTC
AGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTT
TATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGATCTGTCTCGTAACTG
TGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACA
TTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATAC
ACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAA
AGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAA
CATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGA
AAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCA
AATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCT
TCATTACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCG
ACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGG
ATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGA
GTTCATACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCAT
GCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAA
GGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTAC
ACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTC
ATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCT
TGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTC
TTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAAT
GCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATAC
TGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACT
ACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCA
GTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAA
TGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGA
AAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGAC
ATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCA
AAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAA
TGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGA
ATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATG
CTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACT
AGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATC
AAAACTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTT
TTCATATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATAT
ATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352144 ⟹ NP_001339073

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGGACCTCTCTGACCTCATCTCCTGCCTGTGT
CCTCCTCGCTCCCTCTGCTCCAGCCAAGCATGCGTCCTTCCTGTTCCTGGGCCGAGCTTGCTCC
TGCCTCAAGGCCTTCACGTGGGCTGTGCCTCTGCTGGAACTCGCTGGCCCCTCAGCTGCAGAAA
GGTGGGAGACAATGCCTTGGAGCTGCAAATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGT
TTGCTCACATTGACCCGTGCCTTCCCTCAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCC
TGACCCTGTGACATGAACTTCTGAAGAGTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCA
GACATGGATGGAGACGGGTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGA
AATGCCTGAACTCTACACAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCT
GGTCTCCCTGGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAAC
CCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTT
GCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAA
TTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGA
AGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATG
AACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAA
CCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAAT
AAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGG
AAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACG
TCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAA
AAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAAT
GTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAA
ACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAG
AAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGT
CAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGG
CAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCA
TACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAA
TTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACA
CCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAA
GCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACA
AATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCA
TACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTC
ACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCT
TTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAG
AAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATC
AGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACA
GCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTC
AAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGA
GGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGT
GCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATA
ATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAA
TATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352146 ⟹ NP_001339075

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGACCTCTCT
GACCTCATCTCCTGCCTGTGTCCTCCTCGCTCCCTCTGCTCCAGCCAAGCATGCGTCCTTCCTG
TTCCTGGGCCGAGCTTGCTCCTGCCTCAAGGCCTTCACGTGGGCTGTGCCTCTGCTGGAACTCG
CTGGCCCCTCAGCTGCAGCATTGACTTCCAAAGACTCCTGGCACATGAGGAAGAAACCCAGAAG
AGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGGGACGTGGCCATCGAAT
TCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTATACAGGGATGTGATGTT
GGAGAACTACAGGAACCTGGTCTCCCTGGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCA
CCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAAC
ATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTG
GAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGG
AGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCT
TTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCA
TGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATC
AAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAAC
AGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGG
CTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGT
GGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAAC
CATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAG
AGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCA
TGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCA
AAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTA
CAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATT
CACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCC
TTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGT
TTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAG
TGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATA
CTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAAC
TACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTT
AGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTA
GTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAA
GGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGT
CATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTC
ACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAA
ACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATAC
ACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAA
CATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAA
GGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAG
AACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGAT
GTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352147 ⟹ NP_001339076

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCCATTGACTT
CCAAAGACTCCTGGCACATGAGGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCT
TTTACTCAGTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGA
ACTCTACACAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCT
GGATCCATCTGTGATAGCCTCTCTTCTTATCCAAGCAAAGGGCTGAGATTCTTGAAAAGCCACA
GCACATCATGTTCCATTCATTTTATAAGCGGGAAATTCTCTTCCTGACCAGAGTATTATCCTAT
GTGGGAGCACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAA
GGGTGGGAATGGATCAAAGGTGTGAAAACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAG
CACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAA
ACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAG
TGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTA
GGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAG
CTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAAC
CATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCA
TCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGA
ACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCAT
GGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGT
GTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAA
ACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGG
AGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATT
CATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGG
CAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCT
TACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAA
TTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAG
CCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAG
GTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACA
AGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCA
TACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTA
ACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCT
TTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATG
TAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACT
AAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGA
GTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAG
TCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGC
AAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATAT
ACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTA
AACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCC
AAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGT
AGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGG
ATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352148 ⟹ NP_001339077

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGAAAGGTGGGAGACAATGCCTTGGAGCTGCA
AATCTTCTCTGAGTCTGAAGCATCCTGCCTGACGCGTTTGCTCACATTGACCCGTGCCTTCCCT
CAGTCCTTCTCATCTCTACTGAGATTCCGTCTCACCCTGACCCTGTGACATGAACTTCTGAAGA
GTCCACTGGGCATGGTCCTGGGAAGGGCTCACACCCAGACATGGATGGAGACGGGTTGACATTC
AGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTT
TATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGATCCATCTGTGATAGC
CTCTCTTCTTATCCAAGCAAAGGGCTGAGATTCTTGAAAAGCCACAGCACATCATGTTCCATTC
ATTTTATAAGCGGGAAATTCTCTTCCTGACCAGAGTATTATCCTATGTGGGAGCACAGGAAAGA
GCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAAGGGTGGGAATGGATCAAA
GGTGTGAAAACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTA
ACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTT
TTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGA
AATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATA
GAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCA
TGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTC
AACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTA
ATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAG
GGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTA
CGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTC
AAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGA
ATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAG
AAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATC
AGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAG
GTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGT
GGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAAC
CATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAG
AATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCA
CACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGA
AAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTA
CAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATC
CATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACC
TCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTC
CTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAA
AGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATA
TCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACA
CAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGT
TCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCA
GAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTT
GTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAA
TAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCA
AATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352149 ⟹ NP_001339078

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGACCTCTCT
GACCTCATCTCCTGCCTGTGTCCTCCTCGCTCCCTCTGCTCCAGCCAAGCATGCGTCCTTCCTG
TTCCTGGGCCGAGCTTGCTCCTGCCTCAAGGCCTTCACGTGGGCTGTGCCTCTGCTGGAACTCG
CTGGCCCCTCAGCTGCAGCATTGACTTCCAAAGACTCCTGGCACATGAGGAAGAAACCCAGAAG
AGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGGGACGTGGCCATCGAAT
TCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTATACAGGGATGTGATGTT
GGAGAACTACAGGAACCTGGTCTCCCTGGATCCATCTGTGATAGCCTCTCTTCTTATCCAAGCA
AAGGGCTGAGATTCTTGAAAAGCCACAGCACATCATGTTCCATTCATTTTATAAGCGGGAAATT
CTCTTCCTGACCAGAGTATTATCCTATGTGGGAGCACAGGAAAGAGCCCTGGACCATAGAAAGC
CAAGTACGAGTAGCAAGAAAACCAAAAGGGTGGGAATGGATCAAAGGTGTGAAAACAGATCTGT
CTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCA
CACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAG
AAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTA
CGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAA
GTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAA
GCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTT
CACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTT
CATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATAT
ATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTG
GAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCG
TCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGT
CGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATG
AGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGA
GAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCAT
CAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGA
CTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATG
TGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAA
CCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGA
GAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTC
GAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGC
AAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTT
ACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAAT
CCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAAC
CTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGG
TCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAA
GTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCAT
TCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATC
AGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTC
ACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTA
ACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGC
TGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACAC
AACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352150 ⟹ NP_001339079

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCCATTGACTT
CCAAAGACTCCTGGCACATGAGGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCT
TTTACTCAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCC
AGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGC
TTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATT
GCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAG
AGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAA
CTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACC
ATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAA
ATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGGAA
AAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTC
AGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAA
ATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAATGT
GACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAAC
CTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAA
AACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCA
ACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCA
AGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATA
CAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATT
CATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACC
TTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGC
CTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAA
TGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATA
CTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCAC
TAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTT
AGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAA
ATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAG
AGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGC
ATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAA
GCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGG
CTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGC
ATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAAT
TCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAATA
TGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_001352151 ⟹ NP_001339080

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGAC
CCTCTGTGTAGATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGAT
ACGGCCCTTAAAATCCCCGTACACTCCACCCCAGGACCTCTCTGACCTCATCTCCTGCCTGTGT
CCTCCTCGCTCCCTCTGCTCCAGCCAAGCATGCGTCCTTCCTGTTCCTGGGCCGAGCTTGCTCC
TGCCTCAAGGCCTTCACGTGGGCTGTGCCTCTGCTGGAACTCGCTGGCCCCTCAGCTGCAGCAT
TGACTTCCAAAGACTCCTGGCACATGAGGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGA
ATGGCTTTTACTCAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGG
TAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAG
TTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAA
GAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGA
TAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCC
CATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTG
TCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTC
TAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATT
AGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTG
TACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAG
TCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAAT
GAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAG
AGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACA
TCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTG
AGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAAT
GTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAA
ACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGG
AGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATT
CACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGG
GAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCT
TACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCA
TCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAA
CCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAG
TCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATA
AAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTA
TATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTA
CACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAA
GTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGG
CAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATT
TTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGG
AATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCC
CAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

NM_018355 ⟹ NP_060825

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI
GRCh37	19	53,611,132 - 53,636,173 (-)	RGD
Build 36	19	58,302,944 - 58,327,957 (-)	NCBI Archive
Celera	19	50,658,663 - 50,683,384 (-)	RGD
HuRef	19	49,935,622 - 49,960,144 (-)	ENTREZGENE
CHM1_1	19	53,612,901 - 53,637,963 (-)	NCBI
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

Sequence:

show sequence

AGTTTCCTACAGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCCATTGACTT
CCAAAGACTCCTGGCACATGAGGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCT
TTTACTCAGTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGA
ACTCTACACAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCT
GGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAA
GTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGG
AAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAA
AGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATA
GGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGC
AGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTC
CTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAAATATGGG
ACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGGAAAAACCTT
ACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTCAGGTAAG
TCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAAC
CTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAATGTGACAGAA
GTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAA
ATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAAACTCAT
ATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTA
CCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTT
CAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGT
AATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTG
GAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAG
TCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGT
GTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATC
AATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGA
AAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACAT
CAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGC
GCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATA
TGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAA
CCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAG
AATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCA
TTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGGCTTCATT
TAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGA
AGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAATTCAGTCT
AGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAA
ACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

XM_006723267 ⟹ XP_006723330

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

Sequence:

show sequence

AGGCCCGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGACCCTCTGTGTA
GATTAAACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGATACGGCCCTTA
AAATCCCCGTACACTCCACCCCAGCATTGACTTCCAAAGACTCCTGGCACATGAGGAAGAAACC
CAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGGGACGTGGCCA
TCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTATACAGGGATGT
GATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGAGTATTATCCTATGTGGGAGCACAGGAAA
GAGCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAAGGGTGGGAATGGATCA
AAGGTGTGAAAACAGATGGAGTTTCGCTCTTATTGCCCAGGCTGGAGTGCAATGGTGCAATCTC
GGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTCCTGCCTCAGCCTCCCGAGTAGCT
GGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACC
CAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTG
CTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAAT
TGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAA
GAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGA
ACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAAC
CATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATA
AATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGGA
AAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACGT
CAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAA
AATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAATG
TGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAA
CCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGA
AAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTC
AACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGC
AAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCAT
ACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAAT
TCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACAC
CTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAG
CCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAA
ATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCAT
ACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCA
CTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTT
TAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGA
AATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCA
GAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAG
CATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCA
AGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAG
GCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTG
CATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAA
TTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAAT
ATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

XM_017026960 ⟹ XP_016882449

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

Sequence:

show sequence

TGGGTGAAGGTGACGGCGTCGAGCTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATG
AGTGGAAATGCCTGAACTCTACACAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAG
GAACCTGGTCTCCCTGGAGTATTATCCTATGTGGGAGCACAGGAAAGAGCCCTGGACCATAGAA
AGCCAAGTACGAGTAGCAAGAAAACCAAAAGGGTGGGAATGGATCAAAGGTGTGAAAACAGGCT
GGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTCCT
GCCTCAGCCTCCCGAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAG
CACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAA
ACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAG
TGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTA
GGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAG
CTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAAC
CATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCA
TCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGA
ACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCAT
GGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGT
GTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAA
ACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGG
AGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATT
CATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGG
CAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCT
TACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAA
TTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAG
CCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAG
GTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACA
AGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCA
TACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTA
ACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCT
TTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATG
TAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACT
AAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGA
GTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAG
TCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGC
AAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATAT
ACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTA
AACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCC
AAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGT
AGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGG
ATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

XM_017026964 ⟹ XP_016882453

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

Sequence:

show sequence

GGGTGAAGGTGACGGCGTCGAGCGTGAGTGACCCTCTGTGTAGATTAAACCTGCGCTCCCTGTT
TCCCATTTCCACAGCCGATGTCCAGGGTCGATACGGCCCTTAAAATCCCCGTACACTCCACCCC
AGGACCTCTCTGACCTCATCTCCTGCCTGTGTCCTCCTCGCTCCCTCTGCTCCAGCCAAGCATG
CGTCCTTCCTGTTCCTGGGCCGAGCTTGCTCCTGCCTCAAGGCCTTCACGTGGGCTGTGCCTCT
GCTGGAACTCGCTGGCCCCTCAGCTGCAGCATTGACTTCCAAAGACTCCTGGCACATGAGGAAG
AAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGGGACGT
GGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTATACAGG
GATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGATCTGTCTCGTAACTGTGTAATCA
AGGAACTAGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACA
ACATGAAAAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTT
GACTGTCAGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATC
TTACTTGTAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCT
TGGATTAAGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTAT
GAATGTAACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTT
CTTCTACCATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACT
CACACAAGAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCC
TTGAATCATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAAT
GTGATCTGTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATAC
TGGAGAGAAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCA
CTACATCGGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCA
GTCGAAATTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAA
AGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGC
AAGAAACCTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTC
ATCAGAGAATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCA
GACTTCAAGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAA
TGTGGTAAGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGA
AACCTTACAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCA
GGTCATCCATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCAT
TCAAGCCTAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTG
GCAAATCCTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACC
TTACAAATGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATT
ATCCATACTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAA
ATCCTGTGAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAA
GGTTTTCAGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTAC
GAGTACAGCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAG
AAATCATATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCA
AAATGTGTAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGT
AACACATCCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATT
ACACATTGTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAA
GGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

XM_017026969 ⟹ XP_016882458

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

Sequence:

show sequence

CGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGACCCTCTGTGTAGATTA
AACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGATACGGCCCTTAAAATC
CCCGTACACTCCACCCCAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGG
AAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGA
AGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGAT
GAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAAC
GCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACA
TCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAG
TCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATG
TTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATG
CATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATG
ACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCT
TTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATG
TAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACT
GGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCAC
TACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAG
TGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAAT
GAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGG
AGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCA
TTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTAC
AATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGT
GTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAA
GCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAG
GTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCC
CAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGG
GAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCT
TATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAA
TTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACT
CCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATC
ACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGT
GTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTA
TATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGT
GAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCA
AGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTC
A

hide sequence

RefSeq Acc Id:

XM_024451595 ⟹ XP_024307363

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,129,686 (-)	NCBI

Sequence:

show sequence

CCTGGCCTCAAGTAATCTCCCCTCCTTCAGCCTCGAAGTGCTGGGATTACAGGCACGAGCCAAC
ATGCCTGGCCAGTCCTGGAATTTTCTAAGGGAGATGTGATAAAGGCAAACACAGCCCATTGGCC
CTTCCAGGTCGTGACATCATAATTCAGCCACATCTCCTCCTTCTCACTCAACTCAGACCTCTCA
GGATAACTTGGTGAAATGACTCCCTCTCTCAGCCTCAGTGAGCCCACCTGTAACAGAGATAAGG
GACTAGACCAGAAAACCTCAATCATTGACTTCCAAAGACTCCTGGCACATGAGGAAGAAACCCA
GAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGGGACGTGGCCATC
GAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTATACAGGGATGTGA
TGTTGGAGAACTACAGGAACCTGGTCTCCCTGGAGTATTATCCTATGTGGGAGCACAGGAAAGA
GCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAAGGGTGGGAATGGATCAAA
GGTGTGAAAACAGATGGAGTTTCGCTCTTATTGCCCAGGCTGGAGTGCAATGGTGCAATCTCGG
CTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGG
GATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAGGTAACCCA
GGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGAGTTTTGCT
TCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAAAGAAATTG
CAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCGATAGAAGA
GGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCCCCATGAAC
TGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCTGTCAACCA
TGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTTCTAATAAA
TATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCATTAGGGAAA
AACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACTGTACGTCA
GGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTAGTCAAAAA
TCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAATGAATGTG
ACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGAGAGAAACC
TTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTACATCAGAAA
ACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGTGAGGTCAA
CACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAATGTGGCAA
GGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGAAACCATAC
AAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTGGAGAATTC
ATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAATTCACACCT
TGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTGGGAAAGCC
TTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCCTTACAAAT
GTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTCATCCATAC
TGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAAACCTCACT
AGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAAGTCCTTTA
GTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTATAAAAGAAA
TTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTTATATCAGA
GAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCTACACAGCA
TCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACAAGTTCAAG
CATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTGGCAGAGGC
TTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATATTTTGTGCA
TGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAGGAATAATT
CAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGCCCAAATAT
GTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

XM_024451596 ⟹ XP_024307364

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

Sequence:

show sequence

CGGAAACGGATCGCGTTGGGTGAAGGTGACGGCGTCGAGCGTGAGTGACCCTCTGTGTAGATTA
AACCTGCGCTCCCTGTTTCCCATTTCCACAGCCGATGTCCAGGGTCGATACGGCCCTTAAAATC
CCCGTACACTCCACCCCAGGACCTCTCTGACCTCATCTCCTGCCTGTGTCCTCCTCGCTCCCTC
TGCTCCAGCCAAGCATGCGTCCTTCCTGTTCCTGGGCCGAGCTTGCTCCTGCCTCAAGGCCTTC
ACGTGGGCTGTGCCTCTGCTGGAACTCGCTGGCCCCTCAGCTGCAGCATTGACTTCCAAAGACT
CCTGGCACATGAGGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAG
TTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACAC
AGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGAGTATTA
TCCTATGTGGGAGCACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAA
CCAAAAGGGTGGGAATGGATCAAAGGTGTGAAAACAGATGGAGTTTCGCTCTTATTGCCCAGGC
TGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTCC
TGCCTCAGCCTCCCGAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTA
GCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAA
AACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCA
GTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGT
AGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAA
GCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAA
CCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACC
ATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAG
AACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCA
TGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTG
TGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGA
AACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCG
GAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAAT
TCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTG
GCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACC
TTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGA
ATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAA
GCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAA
GGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTAC
AAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCC
ATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCT
AACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCC
TTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAAT
GTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATAC
TAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTG
AGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCA
GTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAG
CAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATA
TACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGT
AAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATC
CAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTG
TAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAG
GATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

XM_024451597 ⟹ XP_024307365

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

Sequence:

show sequence

TCCTTCAGGCTGCCCGGGCTCTTCTCTCCGCGCATGCGCAGTTTCCTACAGGCCCGGAAACGGA
TCGCGTTGGGTGAAGGTGACGGCGTCGAGCCATTGACTTCCAAAGACTCCTGGCACATGAGGAA
GAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGGGACG
TGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTATACAG
GGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGAGTATTATCCTATGTGGGAGCAC
AGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAAGGGTGGGAAT
GGATCAAAGGTGTGAAAACAGATGGAGTTTCGCTCTTATTGCCCAGGCTGGAGTGCAATGGTGC
AATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTCCTGCCTCAGCCTCCCGA
GTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGGAAG
GTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGAAGA
GTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGATGAA
AGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAACGCG
ATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACATCC
CCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAGTCT
GTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATGTTT
CTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATGCAT
TAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATGACT
GTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCTTTA
GTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATGTAA
TGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACTGGA
GAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCACTAC
ATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAGTGT
GAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAATGAA
TGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGGAGA
AACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCATTG
GAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTACAAT
TCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGTGTG
GGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAAGCC
TTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAGGTC
ATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCCCAA
ACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGGGAA
GTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCTTAT
AAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAATTT
ATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACTCCT
ACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATCACA
AGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGTGTG
GCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTATAT
TTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGTGAG
GAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCAAGC
CCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

XM_024451598 ⟹ XP_024307366

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,129,686 (-)	NCBI

Sequence:

show sequence

TGACTCCCTCTCTCAGCCTCAGTGAGCCCACCTGTAACAGAGATAAGGGACTAGACCAGAAAAC
CTCAATGACCTCTCTGACCTCATCTCCTGCCTGTGTCCTCCTCGCTCCCTCTGCTCCAGCCAAG
CATGCGTCCTTCCTGTTCCTGGGCCGAGCTTGCTCCTGCCTCAAGGCCTTCACGTGGGCTGTGC
CTCTGCTGGAACTCGCTGGCCCCTCAGCTGCAGCATTGACTTCCAAAGACTCCTGGCACATGAG
GAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCAGTTGACATTCAGGG
ACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACACAGAGGACTTTATA
CAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGAGTATTATCCTATGTGGGAG
CACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAAACCAAAAGGGTGGG
AATGGATCAAAGGTGTGAAAACAGATGGAGTTTCGCTCTTATTGCCCAGGCTGGAGTGCAATGG
TGCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTCCTGCCTCAGCCTCC
CGAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACTAGCACCACAACAGG
AAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAAAAACATGACATTGA
AGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTCAGTGGAGAGATGAT
GAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTGTAGGAGAGACCAAC
GCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTAAGCTTTCTACCACA
TCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTAACCATGTTGAGAAG
TCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTACCATCAAAACCCATG
TTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAAGAACAGAAATCATG
CATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATCATGGCTCACACATG
ACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCTGTGTGGCAAGGTCT
TTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAGAAACCATACAAATG
TAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATCGGAGAGTTCACACT
GGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAATTCATGCCTTGCAC
TACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGTGGCAAAGCCTTTAG
TGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAACCTTACAAATGCAAT
GAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAGAATTCACACTGGGG
AGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCAAGCCTTGCAAGGCA
TTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTAAGGTTTTCAGTTAC
AATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTACAAGTGTAATGAGT
GTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATCCATACTGGAGAGAA
GCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCCTAACTACCCATCAG
GTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATCCTTTAGTGTGCGCC
CAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAATGTAGTGATTGTGG
GAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATACTAAGGAGAAACCT
TATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGTGAGTCATCAAAGAA
TTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTCAGTCACAATTCACT
CCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACAGCAAACCCTTCATC
ACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCATATACACCTAACTGT
GTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTGTAAACATCTTTGTA
TATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACATCCAAGGATTTATGT
GAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATTGTAGAACAAATGCA
AGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCAGGATGTTTGAAGTC
A

hide sequence

RefSeq Acc Id:

XM_024451599 ⟹ XP_024307367

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

Sequence:

show sequence

TGAAGGTGACGGCGTCGAGCGACCTCTCTGACCTCATCTCCTGCCTGTGTCCTCCTCGCTCCCT
CTGCTCCAGCCAAGCATGCGTCCTTCCTGTTCCTGGGCCGAGCTTGCTCCTGCCTCAAGGCCTT
CACGTGGGCTGTGCCTCTGCTGGAACTCGCTGGCCCCTCAGCTGCAGCATTGACTTCCAAAGAC
TCCTGGCACATGAGGAAGAAACCCAGAAGAGGAGAGCAAAGGAGTCAGGAATGGCTTTTACTCA
GTTGACATTCAGGGACGTGGCCATCGAATTCTCTCAAGATGAGTGGAAATGCCTGAACTCTACA
CAGAGGACTTTATACAGGGATGTGATGTTGGAGAACTACAGGAACCTGGTCTCCCTGGAGTATT
ATCCTATGTGGGAGCACAGGAAAGAGCCCTGGACCATAGAAAGCCAAGTACGAGTAGCAAGAAA
ACCAAAAGGGTGGGAATGGATCAAAGGTGTGAAAACAGATGGAGTTTCGCTCTTATTGCCCAGG
CTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTTCGCCTCCCGGATTCAAATGATTCTC
CTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGATCTGTCTCGTAACTGTGTAATCAAGGAACT
AGCACCACAACAGGAAGGTAACCCAGGAGAAGTATTCCACACAGTGACATTGGAACAACATGAA
AAACATGACATTGAAGAGTTTTGCTTCAGGGAAATCAAGAAAAAAATACACGACTTTGACTGTC
AGTGGAGAGATGATGAAAGAAATTGCAACAAAGTGACTACGGCCCCAAAAGAAAATCTTACTTG
TAGGAGAGACCAACGCGATAGAAGAGGTATAGGAAACAAGTCTATTAAACATCAGCTTGGATTA
AGCTTTCTACCACATCCCCATGAACTGCAGCAGTTTCAAGCTGAAGGGAAAATTTATGAATGTA
ACCATGTTGAGAAGTCTGTCAACCATGGTTCCTCAGTTTCACCACCCCAAATAATTTCTTCTAC
CATCAAAACCCATGTTTCTAATAAATATGGGACTGATTTCATCTGTTCTTCATTACTCACACAA
GAACAGAAATCATGCATTAGGGAAAAACCTTACAGATATATTGAGTGCGACAAAGCCTTGAATC
ATGGCTCACACATGACTGTACGTCAGGTAAGTCATTCTGGAGAGAAAGGATATAAATGTGATCT
GTGTGGCAAGGTCTTTAGTCAAAAATCAAACCTTGCGCGTCATTGGAGAGTTCATACTGGAGAG
AAACCATACAAATGTAATGAATGTGACAGAAGTTTCAGTCGCAACTCATGCCTTGCACTACATC
GGAGAGTTCACACTGGAGAGAAACCTTACAAATGTTATGAGTGTGACAAGGTCTTCAGTCGAAA
TTCATGCCTTGCACTACATCAGAAAACTCATATTGGAGAGAAACCTTACACATGTAAAGAGTGT
GGCAAAGCCTTTAGTGTGAGGTCAACACTTACCAACCATCAGGTAATTCATAGTGGCAAGAAAC
CTTACAAATGCAATGAATGTGGCAAGGTGTTCAGTCAGACTTCAAGCCTTGCAACTCATCAGAG
AATTCACACTGGGGAGAAACCATACAAGTGTAATGAATGTGGTAAAGTCTTCAGTCAGACTTCA
AGCCTTGCAAGGCATTGGAGAATTCATACTGGAGAGAAACCTTACAAATGCAATGAATGTGGTA
AGGTTTTCAGTTACAATTCACACCTTGCGAGTCATCGGAGAGTTCATACTGGAGAGAAACCTTA
CAAGTGTAATGAGTGTGGGAAAGCCTTTAGTGTGCATTCGAACTTAACTACCCATCAGGTCATC
CATACTGGAGAGAAGCCTTACAAATGTAATCAATGTGGCAAAGGCTTCAGTGTGCATTCAAGCC
TAACTACCCATCAGGTCATCCATACTGGAGAAAAACCTTACAAATGTAATGAGTGTGGCAAATC
CTTTAGTGTGCGCCCAAACCTCACTAGACATCAGATAATCCATACTGGAAAGAAACCTTACAAA
TGTAGTGATTGTGGGAAGTCCTTTAGTGTGCGCCCAAACCTCTTCAGACATCAAATTATCCATA
CTAAGGAGAAACCTTATAAAAGAAATTAATATGGCAAGGTCTTCAGTCAAAGTTTAAATCCTGT
GAGTCATCAAAGAATTTATATCAGAGAGAAACCATACAAGTATAATAAATGTGGCAAGGTTTTC
AGTCACAATTCACTCCTACACAGCATCAGAGAATTTCATTCTTGAGAGAATCCTTACGAGTACA
GCAAACCCTTCATCACAAGTTCAAGCATTCATTGACATCAGAGTCCATGCTAAAGAGAAATCAT
ATACACCTAACTGTGTGGCAGAGGCTTCATTTAGGTCTCACAACTCACTAGACATCAAAATGTG
TAAACATCTTTGTATATTTTGTGCATGTTGAAGCTATTAACCAAGGATCAAAACTGTAACACAT
CCAAGGATTTATGTGAGGAATAATTCAGTCTAGTTGTGCTGATAAACTTTTCATATTACACATT
GTAGAACAAATGCAAGCCCAAATATGTTAAAACTCACACAACATGATATATATTAAAGGTTGCA
GGATGTTTGAAGTCA

hide sequence

RefSeq Acc Id:

XM_047439079 ⟹ XP_047295035

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,129,686 (-)	NCBI

RefSeq Acc Id:

XM_047439080 ⟹ XP_047295036

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,129,686 (-)	NCBI

RefSeq Acc Id:

XM_047439081 ⟹ XP_047295037

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,129,686 (-)	NCBI

RefSeq Acc Id:

XM_047439082 ⟹ XP_047295038

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,129,686 (-)	NCBI

RefSeq Acc Id:

XM_047439083 ⟹ XP_047295039

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

RefSeq Acc Id:

XM_047439084 ⟹ XP_047295040

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

RefSeq Acc Id:

XM_047439085 ⟹ XP_047295041

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,129,686 (-)	NCBI

RefSeq Acc Id:

XM_047439086 ⟹ XP_047295042

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

RefSeq Acc Id:

XM_047439087 ⟹ XP_047295043

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

RefSeq Acc Id:

XM_047439088 ⟹ XP_047295044

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

RefSeq Acc Id:

XM_047439089 ⟹ XP_047295045

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

RefSeq Acc Id:

XM_047439090 ⟹ XP_047295046

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,107,879 - 53,132,910 (-)	NCBI

RefSeq Acc Id:

XM_047439091 ⟹ XP_047295047

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,115,799 - 53,129,686 (-)	NCBI

RefSeq Acc Id:

XM_054321419 ⟹ XP_054177394

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,211,977 (-)	NCBI

RefSeq Acc Id:

XM_054321420 ⟹ XP_054177395

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,211,977 (-)	NCBI

RefSeq Acc Id:

XM_054321421 ⟹ XP_054177396

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,211,977 (-)	NCBI

RefSeq Acc Id:

XM_054321422 ⟹ XP_054177397

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,211,977 (-)	NCBI

RefSeq Acc Id:

XM_054321423 ⟹ XP_054177398

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

RefSeq Acc Id:

XM_054321424 ⟹ XP_054177399

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

RefSeq Acc Id:

XM_054321425 ⟹ XP_054177400

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

RefSeq Acc Id:

XM_054321426 ⟹ XP_054177401

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,211,977 (-)	NCBI

RefSeq Acc Id:

XM_054321427 ⟹ XP_054177402

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

RefSeq Acc Id:

XM_054321428 ⟹ XP_054177403

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,211,977 (-)	NCBI

RefSeq Acc Id:

XM_054321429 ⟹ XP_054177404

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

RefSeq Acc Id:

XM_054321430 ⟹ XP_054177405

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

RefSeq Acc Id:

XM_054321431 ⟹ XP_054177406

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,211,977 (-)	NCBI

RefSeq Acc Id:

XM_054321432 ⟹ XP_054177407

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,198,692 (-)	NCBI

RefSeq Acc Id:

XM_054321433 ⟹ XP_054177408

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

RefSeq Acc Id:

XM_054321434 ⟹ XP_054177409

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

RefSeq Acc Id:

XM_054321435 ⟹ XP_054177410

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

RefSeq Acc Id:

XM_054321436 ⟹ XP_054177411

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,190,480 - 56,215,200 (-)	NCBI

RefSeq Acc Id:

XM_054321437 ⟹ XP_054177412

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	56,198,087 - 56,211,977 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001129510	(Get FASTA)	NCBI Sequence Viewer
	NP_001157781	(Get FASTA)	NCBI Sequence Viewer
	NP_001317688	(Get FASTA)	NCBI Sequence Viewer
	NP_001317695	(Get FASTA)	NCBI Sequence Viewer
	NP_001339059	(Get FASTA)	NCBI Sequence Viewer
	NP_001339060	(Get FASTA)	NCBI Sequence Viewer
	NP_001339061	(Get FASTA)	NCBI Sequence Viewer
	NP_001339062	(Get FASTA)	NCBI Sequence Viewer
	NP_001339063	(Get FASTA)	NCBI Sequence Viewer
	NP_001339064	(Get FASTA)	NCBI Sequence Viewer
	NP_001339065	(Get FASTA)	NCBI Sequence Viewer
	NP_001339066	(Get FASTA)	NCBI Sequence Viewer
	NP_001339067	(Get FASTA)	NCBI Sequence Viewer
	NP_001339068	(Get FASTA)	NCBI Sequence Viewer
	NP_001339069	(Get FASTA)	NCBI Sequence Viewer
	NP_001339070	(Get FASTA)	NCBI Sequence Viewer
	NP_001339071	(Get FASTA)	NCBI Sequence Viewer
	NP_001339072	(Get FASTA)	NCBI Sequence Viewer
	NP_001339073	(Get FASTA)	NCBI Sequence Viewer
	NP_001339075	(Get FASTA)	NCBI Sequence Viewer
	NP_001339076	(Get FASTA)	NCBI Sequence Viewer
	NP_001339077	(Get FASTA)	NCBI Sequence Viewer
	NP_001339078	(Get FASTA)	NCBI Sequence Viewer
	NP_001339079	(Get FASTA)	NCBI Sequence Viewer
	NP_001339080	(Get FASTA)	NCBI Sequence Viewer
	NP_060825	(Get FASTA)	NCBI Sequence Viewer
	XP_006723330	(Get FASTA)	NCBI Sequence Viewer
	XP_016882449	(Get FASTA)	NCBI Sequence Viewer
	XP_016882453	(Get FASTA)	NCBI Sequence Viewer
	XP_016882458	(Get FASTA)	NCBI Sequence Viewer
	XP_024307363	(Get FASTA)	NCBI Sequence Viewer
	XP_024307364	(Get FASTA)	NCBI Sequence Viewer
	XP_024307365	(Get FASTA)	NCBI Sequence Viewer
	XP_024307366	(Get FASTA)	NCBI Sequence Viewer
	XP_024307367	(Get FASTA)	NCBI Sequence Viewer
	XP_047295035	(Get FASTA)	NCBI Sequence Viewer
	XP_047295036	(Get FASTA)	NCBI Sequence Viewer
	XP_047295037	(Get FASTA)	NCBI Sequence Viewer
	XP_047295038	(Get FASTA)	NCBI Sequence Viewer
	XP_047295039	(Get FASTA)	NCBI Sequence Viewer
	XP_047295040	(Get FASTA)	NCBI Sequence Viewer
	XP_047295041	(Get FASTA)	NCBI Sequence Viewer
	XP_047295042	(Get FASTA)	NCBI Sequence Viewer
	XP_047295043	(Get FASTA)	NCBI Sequence Viewer
	XP_047295044	(Get FASTA)	NCBI Sequence Viewer
	XP_047295045	(Get FASTA)	NCBI Sequence Viewer
	XP_047295046	(Get FASTA)	NCBI Sequence Viewer
	XP_047295047	(Get FASTA)	NCBI Sequence Viewer
	XP_054177394	(Get FASTA)	NCBI Sequence Viewer
	XP_054177395	(Get FASTA)	NCBI Sequence Viewer
	XP_054177396	(Get FASTA)	NCBI Sequence Viewer
	XP_054177397	(Get FASTA)	NCBI Sequence Viewer
	XP_054177398	(Get FASTA)	NCBI Sequence Viewer
	XP_054177399	(Get FASTA)	NCBI Sequence Viewer
	XP_054177400	(Get FASTA)	NCBI Sequence Viewer
	XP_054177401	(Get FASTA)	NCBI Sequence Viewer
	XP_054177402	(Get FASTA)	NCBI Sequence Viewer
	XP_054177403	(Get FASTA)	NCBI Sequence Viewer
	XP_054177404	(Get FASTA)	NCBI Sequence Viewer
	XP_054177405	(Get FASTA)	NCBI Sequence Viewer
	XP_054177406	(Get FASTA)	NCBI Sequence Viewer
	XP_054177407	(Get FASTA)	NCBI Sequence Viewer
	XP_054177408	(Get FASTA)	NCBI Sequence Viewer
	XP_054177409	(Get FASTA)	NCBI Sequence Viewer
	XP_054177410	(Get FASTA)	NCBI Sequence Viewer
	XP_054177411	(Get FASTA)	NCBI Sequence Viewer
	XP_054177412	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH63880	(Get FASTA)	NCBI Sequence Viewer
	AAH69668	(Get FASTA)	NCBI Sequence Viewer
	AAP35086	(Get FASTA)	NCBI Sequence Viewer
	ABI51309	(Get FASTA)	NCBI Sequence Viewer
	ABI51310	(Get FASTA)	NCBI Sequence Viewer
	ABI51311	(Get FASTA)	NCBI Sequence Viewer
	ABI51312	(Get FASTA)	NCBI Sequence Viewer
	BAA92059	(Get FASTA)	NCBI Sequence Viewer
	BAG53073	(Get FASTA)	NCBI Sequence Viewer
	BBD75048	(Get FASTA)	NCBI Sequence Viewer
	EAW72115	(Get FASTA)	NCBI Sequence Viewer
	EAW72116	(Get FASTA)	NCBI Sequence Viewer
	EAW72117	(Get FASTA)	NCBI Sequence Viewer
	EAW72118	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000243643
	ENSP00000243643.3
	ENSP00000395055
	ENSP00000395055.2
	ENSP00000439435
	ENSP00000439435.1
	ENSP00000468917.1
	ENSP00000469483.1
	ENSP00000469656.1
	ENSP00000470272.1
	ENSP00000470410.1
	ENSP00000471167.1
	ENSP00000471386.1
	ENSP00000471718.1
	ENSP00000471834.1
	ENSP00000472003.1
	ENSP00000472516.1
	ENSP00000472584.1
	ENSP00000472673.1
	ENSP00000472797.1
	ENSP00000472911
	ENSP00000472911.1
	ENSP00000473008.1
GenBank Protein	Q09FC8	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_060825 ⟸ NM_018355
- Peptide Label:	isoform 2
- UniProtKB:	Q09FC8 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAFTQLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLDLSRNCVIKELAPQQEGNP GEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRR GIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNK YGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQK SNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQK THIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPY KCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKA FSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLT RHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN hide sequence

RefSeq Acc Id:	NP_001129510 ⟸ NM_001136038
- Peptide Label:	isoform 1
- UniProtKB:	Q09FC8 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MDGDGLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLDLSRNCVIKELAPQQEGNP GEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRR GIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNK YGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQK SNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQK THIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPY KCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKA FSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLT RHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN hide sequence

RefSeq Acc Id:	NP_001157781 ⟸ NM_001164309
- Peptide Label:	isoform 2
- UniProtKB:	Q09FC8 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAFTQLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLDLSRNCVIKELAPQQEGNP GEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRR GIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNK YGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQK SNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQK THIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPY KCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKA FSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLT RHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN hide sequence

RefSeq Acc Id:

XP_006723330 ⟸ XM_006723267

- Peptide Label:

isoform X5

- Sequence:

show sequence

MAFTQLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLEYYPMWEHRKEPWTIESQV
RVARKPKGWEWIKGVKTDGVSLLLPRLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNC
VIKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPK
ENLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQ
IISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKG
YKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDK
VFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSL
ATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHT
GEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCN
ECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

XP_016882458 ⟸ XM_017026969

- Peptide Label:

isoform X12

- Sequence:

show sequence

MSRVDTALKIPVHSTPDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKI
HDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEG
KIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIEC
DKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNS
CLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVI
HSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYK
CNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGF
SVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFR
HQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

XP_016882449 ⟸ XM_017026960

- Peptide Label:

isoform X6

- Sequence:

show sequence

MPELYTEDFIQGCDVGELQEPGLPGVLSYVGAQERALDHRKPSTSSKKTKRVGMDQRCENRLEC
NGAISAHCNLRLPDSNDSPASASRVAGITDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHEKHD
IEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGLSFL
PHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQEQK
SCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPY
KCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKA
FSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLA
RHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTG
EKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSD
CGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:	XP_016882453 ⟸ XM_017026964
- Peptide Label:	isoform X10
- UniProtKB:	Q09FC8 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAFTQLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLDLSRNCVIKELAPQQEGNP GEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRR GIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNK YGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQK SNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQK THIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPY KCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKA FSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLT RHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN hide sequence

RefSeq Acc Id:

XP_024307365 ⟸ XM_024451597

- Peptide Label:

isoform X5

- Sequence:

show sequence

MAFTQLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLEYYPMWEHRKEPWTIESQV
RVARKPKGWEWIKGVKTDGVSLLLPRLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNC
VIKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPK
ENLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQ
IISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKG
YKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDK
VFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSL
ATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHT
GEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCN
ECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339060 ⟸ NM_001352131

- Peptide Label:

isoform 5

- Sequence:

show sequence

MDGDGLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLEYYPMWEHRKEPWTIESQV
RVARKPKGWEWIKGVKTDGVSLLLPRLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNC
VIKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPK
ENLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQ
IISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKG
YKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDK
VFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSL
ATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHT
GEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCN
ECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339071 ⟸ NM_001352142

- Peptide Label:

isoform 1

- Sequence:

show sequence

MDGDGLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLDLSRNCVIKELAPQQEGNP
GEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRR
GIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNK
YGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQK
SNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQK
THIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPY
KCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKA
FSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLT
RHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339067 ⟸ NM_001352138

- Peptide Label:

isoform 8

- Sequence:

show sequence

MPELYTEDFIQGCDVGELQEPGLPGLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNCV
IKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKE
NLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQI
ISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGY
KCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKV
FSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLA
THQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTG
EKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNE
CGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339065 ⟸ NM_001352136

- Peptide Label:

isoform 7

- Sequence:

show sequence

MDGDGLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLEYYPMWEHRKEPWTIESQV
RVARKPKGWEWIKGVKTDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKK
IHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAE
GKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIE
CDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRN
SCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQV
IHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPY
KCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKG
FSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLF
RHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339061 ⟸ NM_001352132

- Peptide Label:

isoform 3

- Sequence:

show sequence

MPELYTEDFIQGCDVGELQEPGLPGVLSYVGAQERALDHRKPSTSSKKTKRVGMDQRCENRLEC
NGAISAHCNLRLPDSNDSPASASRVAGITDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHEKHD
IEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGLSFL
PHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQEQK
SCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPY
KCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKA
FSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLA
RHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTG
EKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSD
CGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339079 ⟸ NM_001352150

- Peptide Label:

isoform 4

- Sequence:

show sequence

MTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVH
TGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKC
NECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFS
YNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTH
QVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEK
PYKRN

hide sequence

RefSeq Acc Id:

NP_001339068 ⟸ NM_001352139

- Peptide Label:

isoform 8

- Sequence:

show sequence

MPELYTEDFIQGCDVGELQEPGLPGLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNCV
IKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKE
NLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQI
ISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGY
KCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKV
FSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLA
THQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTG
EKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNE
CGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339076 ⟸ NM_001352147

- Peptide Label:

isoform 9

- Sequence:

show sequence

MWEHRKEPWTIESQVRVARKPKGWEWIKGVKTDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHE
KHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGL
SFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQ
EQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGE
KPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKEC
GKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTS
SLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVI
HTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYK
CSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339075 ⟸ NM_001352146

- Peptide Label:

isoform 2

- Sequence:

show sequence

MAFTQLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLDLSRNCVIKELAPQQEGNP
GEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRR
GIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNK
YGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQK
SNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQK
THIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPY
KCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKA
FSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLT
RHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:	NP_001317695 ⟸ NM_001330766
- Peptide Label:	isoform 3
- UniProtKB:	Q09FC8 (UniProtKB/Swiss-Prot), B3KTG1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPELYTEDFIQGCDVGELQEPGLPGVLSYVGAQERALDHRKPSTSSKKTKRVGMDQRCENRLEC NGAISAHCNLRLPDSNDSPASASRVAGITDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHEKHD IEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGLSFL PHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQEQK SCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPY KCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKA FSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLA RHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTG EKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSD CGKSFSVRPNLFRHQIIHTKEKPYKRN hide sequence

RefSeq Acc Id:

NP_001339078 ⟸ NM_001352149

- Peptide Label:

isoform 9

- Sequence:

show sequence

MWEHRKEPWTIESQVRVARKPKGWEWIKGVKTDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHE
KHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGL
SFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQ
EQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGE
KPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKEC
GKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTS
SLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVI
HTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYK
CSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339072 ⟸ NM_001352143

- Peptide Label:

isoform 1

- Sequence:

show sequence

MDGDGLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLDLSRNCVIKELAPQQEGNP
GEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRR
GIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNK
YGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQK
SNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQK
THIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPY
KCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKA
FSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLT
RHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339070 ⟸ NM_001352141

- Peptide Label:

isoform 8

- Sequence:

show sequence

MPELYTEDFIQGCDVGELQEPGLPGLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNCV
IKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKE
NLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQI
ISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGY
KCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKV
FSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLA
THQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTG
EKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNE
CGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339066 ⟸ NM_001352137

- Peptide Label:

isoform 7

- Sequence:

show sequence

MDGDGLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLEYYPMWEHRKEPWTIESQV
RVARKPKGWEWIKGVKTDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKK
IHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAE
GKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIE
CDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRN
SCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQV
IHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPY
KCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKG
FSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLF
RHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339062 ⟸ NM_001352133

- Peptide Label:

isoform 3

- Sequence:

show sequence

MPELYTEDFIQGCDVGELQEPGLPGVLSYVGAQERALDHRKPSTSSKKTKRVGMDQRCENRLEC
NGAISAHCNLRLPDSNDSPASASRVAGITDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHEKHD
IEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGLSFL
PHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQEQK
SCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPY
KCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKA
FSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLA
RHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTG
EKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSD
CGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339059 ⟸ NM_001352130

- Peptide Label:

isoform 5

- Sequence:

show sequence

MDGDGLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLEYYPMWEHRKEPWTIESQV
RVARKPKGWEWIKGVKTDGVSLLLPRLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNC
VIKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPK
ENLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQ
IISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKG
YKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDK
VFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSL
ATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHT
GEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCN
ECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339077 ⟸ NM_001352148

- Peptide Label:

isoform 9

- Sequence:

show sequence

MWEHRKEPWTIESQVRVARKPKGWEWIKGVKTDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHE
KHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGL
SFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQ
EQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGE
KPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKEC
GKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTS
SLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVI
HTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYK
CSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:	NP_001317688 ⟸ NM_001330759
- Peptide Label:	isoform 4
- UniProtKB:	Q09FC8 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVH TGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKC NECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFS YNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTH QVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEK PYKRN hide sequence

RefSeq Acc Id:

NP_001339069 ⟸ NM_001352140

- Peptide Label:

isoform 8

- Sequence:

show sequence

MPELYTEDFIQGCDVGELQEPGLPGLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNCV
IKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKE
NLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQI
ISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGY
KCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKV
FSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLA
THQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTG
EKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNE
CGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339063 ⟸ NM_001352134

- Peptide Label:

isoform 3

- Sequence:

show sequence

MPELYTEDFIQGCDVGELQEPGLPGVLSYVGAQERALDHRKPSTSSKKTKRVGMDQRCENRLEC
NGAISAHCNLRLPDSNDSPASASRVAGITDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHEKHD
IEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGLSFL
PHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQEQK
SCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPY
KCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKA
FSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLA
RHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTG
EKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSD
CGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339073 ⟸ NM_001352144

- Peptide Label:

isoform 1

- Sequence:

show sequence

MDGDGLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLDLSRNCVIKELAPQQEGNP
GEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRR
GIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNK
YGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQK
SNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQK
THIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPY
KCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKA
FSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLT
RHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339080 ⟸ NM_001352151

- Peptide Label:

isoform 4

- Sequence:

show sequence

MTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVH
TGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKC
NECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFS
YNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTH
QVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEK
PYKRN

hide sequence

RefSeq Acc Id:

XP_024307364 ⟸ XM_024451596

- Peptide Label:

isoform X5

- Sequence:

show sequence

MAFTQLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLEYYPMWEHRKEPWTIESQV
RVARKPKGWEWIKGVKTDGVSLLLPRLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNC
VIKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPK
ENLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQ
IISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKG
YKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDK
VFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSL
ATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHT
GEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCN
ECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

XP_024307367 ⟸ XM_024451599

- Peptide Label:

isoform X5

- Sequence:

show sequence

MAFTQLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLEYYPMWEHRKEPWTIESQV
RVARKPKGWEWIKGVKTDGVSLLLPRLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNC
VIKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPK
ENLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQ
IISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKG
YKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDK
VFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSL
ATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHT
GEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCN
ECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

XP_024307363 ⟸ XM_024451595

- Peptide Label:

isoform X2

- Sequence:

show sequence

MTPSLSLSEPTCNRDKGLDQKTSIIDFQRLLAHEEETQKRRAKESGMAFTQLTFRDVAIEFSQD
EWKCLNSTQRTLYRDVMLENYRNLVSLEYYPMWEHRKEPWTIESQVRVARKPKGWEWIKGVKTD
GVSLLLPRLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNCVIKELAPQQEGNPGEVFH
TVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNK
SIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDF
ICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLAR
HWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGE
KPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNEC
GKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHS
NLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQII
HTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

NP_001339064 ⟸ NM_001352135

- Peptide Label:

isoform 6

- Sequence:

show sequence

MTPSLSLSEPTCNRDKGLDQKTSIIDFQRLLAHEEETQKRRAKESGMAFTQLTFRDVAIEFSQD
EWKCLNSTQRTLYRDVMLENYRNLVSLDLSRNCVIKELAPQQEGNPGEVFHTVTLEQHEKHDIE
EFCFREIKKKIHDFDCQWRDDERNCNKVTTAPKENLTCRRDQRDRRGIGNKSIKHQLGLSFLPH
PHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQIISSTIKTHVSNKYGTDFICSSLLTQEQKSC
IREKPYRYIECDKALNHGSHMTVRQVSHSGEKGYKCDLCGKVFSQKSNLARHWRVHTGEKPYKC
NECDRSFSRNSCLALHRRVHTGEKPYKCYECDKVFSRNSCLALHQKTHIGEKPYTCKECGKAFS
VRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSLATHQRIHTGEKPYKCNECGKVFSQTSSLARH
WRIHTGEKPYKCNECGKVFSYNSHLASHRRVHTGEKPYKCNECGKAFSVHSNLTTHQVIHTGEK
PYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCNECGKSFSVRPNLTRHQIIHTGKKPYKCSDCG
KSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

XP_024307366 ⟸ XM_024451598

- Peptide Label:

isoform X5

- Sequence:

show sequence

MAFTQLTFRDVAIEFSQDEWKCLNSTQRTLYRDVMLENYRNLVSLEYYPMWEHRKEPWTIESQV
RVARKPKGWEWIKGVKTDGVSLLLPRLECNGAISAHCNLRLPDSNDSPASASRVAGITDLSRNC
VIKELAPQQEGNPGEVFHTVTLEQHEKHDIEEFCFREIKKKIHDFDCQWRDDERNCNKVTTAPK
ENLTCRRDQRDRRGIGNKSIKHQLGLSFLPHPHELQQFQAEGKIYECNHVEKSVNHGSSVSPPQ
IISSTIKTHVSNKYGTDFICSSLLTQEQKSCIREKPYRYIECDKALNHGSHMTVRQVSHSGEKG
YKCDLCGKVFSQKSNLARHWRVHTGEKPYKCNECDRSFSRNSCLALHRRVHTGEKPYKCYECDK
VFSRNSCLALHQKTHIGEKPYTCKECGKAFSVRSTLTNHQVIHSGKKPYKCNECGKVFSQTSSL
ATHQRIHTGEKPYKCNECGKVFSQTSSLARHWRIHTGEKPYKCNECGKVFSYNSHLASHRRVHT
GEKPYKCNECGKAFSVHSNLTTHQVIHTGEKPYKCNQCGKGFSVHSSLTTHQVIHTGEKPYKCN
ECGKSFSVRPNLTRHQIIHTGKKPYKCSDCGKSFSVRPNLFRHQIIHTKEKPYKRN

hide sequence

RefSeq Acc Id:

ENSP00000471386 ⟸ ENST00000595174

RefSeq Acc Id:

ENSP00000472516 ⟸ ENST00000595193

RefSeq Acc Id:

ENSP00000470272 ⟸ ENST00000595813

RefSeq Acc Id:

ENSP00000473008 ⟸ ENST00000596051

RefSeq Acc Id:

ENSP00000471718 ⟸ ENST00000597877

RefSeq Acc Id:

ENSP00000469656 ⟸ ENST00000597748

RefSeq Acc Id:

ENSP00000468917 ⟸ ENST00000597503

RefSeq Acc Id:

ENSP00000472003 ⟸ ENST00000598024

RefSeq Acc Id:

ENSP00000472673 ⟸ ENST00000598578

RefSeq Acc Id:

ENSP00000471167 ⟸ ENST00000599261

RefSeq Acc Id:

ENSP00000243643 ⟸ ENST00000243643

RefSeq Acc Id:

ENSP00000471834 ⟸ ENST00000600120

RefSeq Acc Id:

ENSP00000469483 ⟸ ENST00000600574

RefSeq Acc Id:

ENSP00000472911 ⟸ ENST00000601493

RefSeq Acc Id:

ENSP00000472797 ⟸ ENST00000601215

RefSeq Acc Id:

ENSP00000470410 ⟸ ENST00000601110

RefSeq Acc Id:

ENSP00000395055 ⟸ ENST00000421033

RefSeq Acc Id:

ENSP00000439435 ⟸ ENST00000500065

RefSeq Acc Id:

ENSP00000472584 ⟸ ENST00000594011

RefSeq Acc Id:	XP_047295046 ⟸ XM_047439090
- Peptide Label:	isoform X13

RefSeq Acc Id:	XP_047295045 ⟸ XM_047439089
- Peptide Label:	isoform X11

RefSeq Acc Id:	XP_047295042 ⟸ XM_047439086
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_047295040 ⟸ XM_047439084
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047295044 ⟸ XM_047439088
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_047295043 ⟸ XM_047439087
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_047295039 ⟸ XM_047439083
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047295041 ⟸ XM_047439085
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047295037 ⟸ XM_047439081
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047295036 ⟸ XM_047439080
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047295035 ⟸ XM_047439079
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047295038 ⟸ XM_047439082
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047295047 ⟸ XM_047439091
- Peptide Label:	isoform X14

RefSeq Acc Id:	XP_054177400 ⟸ XM_054321425
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054177402 ⟸ XM_054321427
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054177411 ⟸ XM_054321436
- Peptide Label:	isoform X12

RefSeq Acc Id:	XP_054177405 ⟸ XM_054321430
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054177399 ⟸ XM_054321424
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054177409 ⟸ XM_054321434
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_054177408 ⟸ XM_054321433
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_054177404 ⟸ XM_054321429
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054177410 ⟸ XM_054321435
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_054177398 ⟸ XM_054321423
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054177406 ⟸ XM_054321431
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054177395 ⟸ XM_054321420
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054177397 ⟸ XM_054321422
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054177396 ⟸ XM_054321421
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054177394 ⟸ XM_054321419
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054177401 ⟸ XM_054321426
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054177403 ⟸ XM_054321428
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054177407 ⟸ XM_054321432
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054177412 ⟸ XM_054321437
- Peptide Label:	isoform X14

Protein Domains

C2H2-type KRAB

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q09FC8-F1-model_v2	AlphaFold	Q09FC8	1-603	view protein structure

Promoters

RGD ID:

13205509

Promoter ID:

EPDNEW_H26335

Type:

initiation region

Name:

ZNF415_3

Description:

zinc finger protein 415

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26336 EPDNEW_H26338

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,129,665 - 53,129,725	EPDNEW

RGD ID:

13205511

Promoter ID:

EPDNEW_H26336

Type:

initiation region

Name:

ZNF415_2

Description:

zinc finger protein 415

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26335 EPDNEW_H26338

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	53,132,900 - 53,132,960	EPDNEW

RGD ID:

6796317

Promoter ID:

HG_KWN:30806

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

ENST00000243643, NM_001136038, NM_001164309, UC002QAU.1, UC002QAV.1, UC002QAX.1, UC002QAY.1, UC002QAZ.1, UC002QBA.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	58,327,621 - 58,328,121 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:20636	AgrOrtholog
COSMIC	ZNF415	COSMIC
Ensembl Genes	ENSG00000170954	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000243643	ENTREZGENE
	ENST00000243643.9	UniProtKB/Swiss-Prot
	ENST00000421033	ENTREZGENE
	ENST00000421033.5	UniProtKB/Swiss-Prot
	ENST00000500065	ENTREZGENE
	ENST00000500065.8	UniProtKB/Swiss-Prot
	ENST00000594011.5	UniProtKB/TrEMBL
	ENST00000595174.5	UniProtKB/TrEMBL
	ENST00000595193.5	UniProtKB/TrEMBL
	ENST00000595813.5	UniProtKB/TrEMBL
	ENST00000596051.1	UniProtKB/TrEMBL
	ENST00000597503.5	UniProtKB/TrEMBL
	ENST00000597748.5	UniProtKB/TrEMBL
	ENST00000597877.1	UniProtKB/TrEMBL
	ENST00000598024.5	UniProtKB/TrEMBL
	ENST00000598578.5	UniProtKB/TrEMBL
	ENST00000599261.5	UniProtKB/TrEMBL
	ENST00000600120.5	UniProtKB/TrEMBL
	ENST00000600574.5	UniProtKB/TrEMBL
	ENST00000601110.5	UniProtKB/TrEMBL
	ENST00000601215.5	UniProtKB/TrEMBL
	ENST00000601493	ENTREZGENE
	ENST00000601493.5	UniProtKB/Swiss-Prot
Gene3D-CATH	6.10.140.140	UniProtKB/TrEMBL
	Classic Zinc Finger	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000170954	GTEx
HGNC ID	HGNC:20636	ENTREZGENE
Human Proteome Map	ZNF415	Human Proteome Map
InterPro	KRAB_dom_sf	UniProtKB/TrEMBL
	Krueppel-associated_box	UniProtKB/TrEMBL
	Znf_C2H2_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_C2H2_type	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:55786	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	55786	ENTREZGENE
OMIM	619506	OMIM
PANTHER	C2H2-TYPE DOMAIN-CONTAINING PROTEIN	UniProtKB/TrEMBL
	KRAB DOMAIN C2H2 ZINC FINGER	UniProtKB/TrEMBL
	KRAB DOMAIN-CONTAINING PROTEIN 5-RELATED	UniProtKB/TrEMBL
	ZINC FINGER AND SCAN DOMAIN-CONTAINING	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC FINGER PROTEIN 83	UniProtKB/Swiss-Prot
Pfam	KRAB	UniProtKB/TrEMBL
	zf-C2H2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134984602	PharmGKB
PROSITE	KRAB	UniProtKB/TrEMBL
	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	KRAB	UniProtKB/TrEMBL
	ZnF_BED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZnF_C2H2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	Krueppel-associated_box	UniProtKB/TrEMBL
	SSF57667	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	B3KTG1	ENTREZGENE, UniProtKB/TrEMBL
	M0QX59_HUMAN	UniProtKB/TrEMBL
	M0QXZ4_HUMAN	UniProtKB/TrEMBL
	M0QZ38_HUMAN	UniProtKB/TrEMBL
	M0QZA6_HUMAN	UniProtKB/TrEMBL
	M0R0D9_HUMAN	UniProtKB/TrEMBL
	M0R0R1_HUMAN	UniProtKB/TrEMBL
	M0R191_HUMAN	UniProtKB/TrEMBL
	M0R1N1_HUMAN	UniProtKB/TrEMBL
	M0R2I1_HUMAN	UniProtKB/TrEMBL
	M0R2T6_HUMAN	UniProtKB/TrEMBL
	M0R358_HUMAN	UniProtKB/TrEMBL
	Q09FC8	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	F5H287	UniProtKB/Swiss-Prot
	Q09FC7	UniProtKB/Swiss-Prot
	Q09FC9	UniProtKB/Swiss-Prot
	Q09FD0	UniProtKB/Swiss-Prot
	Q6NSZ2	UniProtKB/Swiss-Prot
	Q6P3S0	UniProtKB/Swiss-Prot
	Q9NUR2	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