Canonical Allele Identifier: CA1435772659

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301072G= , CM000666.2:g.6301072G=	GRCh38
NC_000004.11:g.6302799G= , CM000666.1:g.6302799G=	GRCh37
NC_000004.10:g.6353700G=	NCBI36
NG_011700.1:g.36223G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.1313G=	ENSP00000507852.1:p.Cys438=
ENST00000683395.1:c.1254G=
ENST00000684087.1:c.1277G=	ENSP00000506978.1:p.Cys426=
ENST00000506362.2:c.1028G=	ENSP00000424103.2:p.Cys343=
ENST00000673642.1:c.936G=	ENSP00000501242.1:p.Leu312=
ENST00000673991.1:c.1313G=	ENSP00000501033.1:p.Cys438=
ENST00000226760.5:c.1277G= MANE Select	ENSP00000226760.1:p.Cys426=
ENST00000503569.5:c.1277G=	ENSP00000423337.1:p.Cys426=
ENST00000507765.1:n.1462G=
NM_001145853.1:c.1277G=	NP_001139325.1:p.Cys426=
NM_006005.3:c.1277G= MANE Select	NP_005996.2:p.Cys426=
XM_017008586.1:c.1286G=	XP_016864075.1:p.Cys429=