Canonical Allele Identifier: CA1435771967

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301846C= , CM000666.2:g.6301846C=	GRCh38
NC_000004.11:g.6303573C= , CM000666.1:g.6303573C=	GRCh37
NC_000004.10:g.6354474C=	NCBI36
NG_011700.1:g.36997C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2087C=	ENSP00000507852.1:p.Ala696=
ENST00000683395.1:c.2028C=
ENST00000684087.1:c.2051C=	ENSP00000506978.1:p.Ala684=
ENST00000506362.2:c.1802C=	ENSP00000424103.2:p.Ala601=
ENST00000673642.1:c.1710C=	ENSP00000501242.1:n.1710C=
ENST00000673991.1:c.2087C=	ENSP00000501033.1:p.Ala696=
ENST00000226760.5:c.2051C= MANE Select	ENSP00000226760.1:p.Ala684=
ENST00000503569.5:c.2051C=	ENSP00000423337.1:p.Ala684=
ENST00000507765.1:n.2236C=
NM_001145853.1:c.2051C=	NP_001139325.1:p.Ala684=
NM_006005.3:c.2051C= MANE Select	NP_005996.2:p.Ala684=
XM_017008586.1:c.2060C=	XP_016864075.1:p.Ala687=