Canonical Allele Identifier: CA1435773399

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301376C= , CM000666.2:g.6301376C=	GRCh38
NC_000004.11:g.6303103C= , CM000666.1:g.6303103C=	GRCh37
NC_000004.10:g.6354004C=	NCBI36
NG_011700.1:g.36527C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1617C=	ENSP00000507852.1:p.Thr539=
ENST00000683395.1:c.1558C=
ENST00000684087.1:c.1581C=	ENSP00000506978.1:p.Thr527=
ENST00000506362.2:c.1332C=	ENSP00000424103.2:p.Thr444=
ENST00000673642.1:c.1240C=	ENSP00000501242.1:p.Leu414=
ENST00000673991.1:c.1617C=	ENSP00000501033.1:p.Thr539=
ENST00000226760.5:c.1581C= MANE Select	ENSP00000226760.1:p.Thr527=
ENST00000503569.5:c.1581C=	ENSP00000423337.1:p.Thr527=
ENST00000507765.1:n.1766C=
NM_001145853.1:c.1581C=	NP_001139325.1:p.Thr527=
NM_006005.3:c.1581C= MANE Select	NP_005996.2:p.Thr527=
XM_017008586.1:c.1590C=	XP_016864075.1:p.Thr530=