Canonical Allele Identifier: CA356174367

Gene: WFS1

Linked Data

• gnomAD v4: 4-6300955-A-T
• MyVariant Identifiers: chr4:g.6302682A>T (hg19) ; chr4:g.6300955A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300955A>T , CM000666.2:g.6300955A>T	GRCh38
NC_000004.11:g.6302682A>T , CM000666.1:g.6302682A>T	GRCh37
NC_000004.10:g.6353583A>T	NCBI36
NG_011700.1:g.36106A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1196A>T	ENSP00000507852.1:p.Asn399Ile
ENST00000683395.1:c.1137A>T
ENST00000684087.1:c.1160A>T	ENSP00000506978.1:p.Asn387Ile
ENST00000506362.2:c.911A>T	ENSP00000424103.2:p.Asn304Ile
ENST00000673642.1:c.819A>T	ENSP00000501242.1:p.Gln273His
ENST00000673991.1:c.1196A>T	ENSP00000501033.1:p.Asn399Ile
ENST00000226760.5:c.1160A>T MANE Select	ENSP00000226760.1:p.Asn387Ile
ENST00000503569.5:c.1160A>T	ENSP00000423337.1:p.Asn387Ile
ENST00000507765.1:n.1345A>T
NM_001145853.1:c.1160A>T	NP_001139325.1:p.Asn387Ile
NM_006005.3:c.1160A>T MANE Select	NP_005996.2:p.Asn387Ile
XM_017008586.1:c.1169A>T	XP_016864075.1:p.Asn390Ile