Canonical Allele Identifier: CA1435772019

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301889C= , CM000666.2:g.6301889C=	GRCh38
NC_000004.11:g.6303616C= , CM000666.1:g.6303616C=	GRCh37
NC_000004.10:g.6354517C=	NCBI36
NG_011700.1:g.37040C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2130C=	ENSP00000507852.1:p.Val710=
ENST00000683395.1:c.2071C=
ENST00000684087.1:c.2094C=	ENSP00000506978.1:p.Val698=
ENST00000506362.2:c.1845C=	ENSP00000424103.2:p.Val615=
ENST00000673642.1:c.1753C=	ENSP00000501242.1:n.1753C=
ENST00000673991.1:c.2130C=	ENSP00000501033.1:p.Val710=
ENST00000226760.5:c.2094C= MANE Select	ENSP00000226760.1:p.Val698=
ENST00000503569.5:c.2094C=	ENSP00000423337.1:p.Val698=
ENST00000507765.1:n.2279C=
NM_001145853.1:c.2094C=	NP_001139325.1:p.Val698=
NM_006005.3:c.2094C= MANE Select	NP_005996.2:p.Val698=
XM_017008586.1:c.2103C=	XP_016864075.1:p.Val701=