Canonical Allele Identifier: CA1435772089

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301941G= , CM000666.2:g.6301941G=	GRCh38
NC_000004.11:g.6303668G= , CM000666.1:g.6303668G=	GRCh37
NC_000004.10:g.6354569G=	NCBI36
NG_011700.1:g.37092G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2182G=	ENSP00000507852.1:p.Ala728=
ENST00000683395.1:c.2123G=
ENST00000684087.1:c.2146G=	ENSP00000506978.1:p.Ala716=
ENST00000506362.2:c.1897G=	ENSP00000424103.2:p.Ala633=
ENST00000673642.1:c.1805G=	ENSP00000501242.1:n.1805G=
ENST00000673991.1:c.2182G=	ENSP00000501033.1:p.Ala728=
ENST00000226760.5:c.2146G= MANE Select	ENSP00000226760.1:p.Ala716=
ENST00000503569.5:c.2146G=	ENSP00000423337.1:p.Ala716=
ENST00000507765.1:n.2331G=
NM_001145853.1:c.2146G=	NP_001139325.1:p.Ala716=
NM_006005.3:c.2146G= MANE Select	NP_005996.2:p.Ala716=
XM_017008586.1:c.2155G=	XP_016864075.1:p.Ala719=