Canonical Allele Identifier: CA1435772698

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301101A= , CM000666.2:g.6301101A=	GRCh38
NC_000004.11:g.6302828A= , CM000666.1:g.6302828A=	GRCh37
NC_000004.10:g.6353729A=	NCBI36
NG_011700.1:g.36252A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1342A=	ENSP00000507852.1:p.Thr448=
ENST00000683395.1:c.1283A=
ENST00000684087.1:c.1306A=	ENSP00000506978.1:p.Thr436=
ENST00000506362.2:c.1057A=	ENSP00000424103.2:p.Thr353=
ENST00000673642.1:c.965A=	ENSP00000501242.1:p.His322=
ENST00000673991.1:c.1342A=	ENSP00000501033.1:p.Thr448=
ENST00000226760.5:c.1306A= MANE Select	ENSP00000226760.1:p.Thr436=
ENST00000503569.5:c.1306A=	ENSP00000423337.1:p.Thr436=
ENST00000507765.1:n.1491A=
NM_001145853.1:c.1306A=	NP_001139325.1:p.Thr436=
NM_006005.3:c.1306A= MANE Select	NP_005996.2:p.Thr436=
XM_017008586.1:c.1315A=	XP_016864075.1:p.Thr439=