Canonical Allele Identifier: CA356174251

Gene: WFS1

Linked Data

• gnomAD v4: 4-6300893-G-T
• MyVariant Identifiers: chr4:g.6302620G>T (hg19) ; chr4:g.6300893G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300893G>T , CM000666.2:g.6300893G>T	GRCh38
NC_000004.11:g.6302620G>T , CM000666.1:g.6302620G>T	GRCh37
NC_000004.10:g.6353521G>T	NCBI36
NG_011700.1:g.36044G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1134G>T	ENSP00000507852.1:p.Gln378His
ENST00000683395.1:c.1075G>T
ENST00000684087.1:c.1098G>T	ENSP00000506978.1:p.Gln366His
ENST00000506362.2:c.849G>T	ENSP00000424103.2:p.Gln283His
ENST00000673642.1:c.757G>T	ENSP00000501242.1:p.Gly253Ter
ENST00000673991.1:c.1134G>T	ENSP00000501033.1:p.Gln378His
ENST00000226760.5:c.1098G>T MANE Select	ENSP00000226760.1:p.Gln366His
ENST00000503569.5:c.1098G>T	ENSP00000423337.1:p.Gln366His
ENST00000506362.1:c.731G>T
ENST00000507765.1:n.1283G>T
NM_001145853.1:c.1098G>T	NP_001139325.1:p.Gln366His
NM_006005.3:c.1098G>T MANE Select	NP_005996.2:p.Gln366His
XM_017008586.1:c.1107G>T	XP_016864075.1:p.Gln369His