Canonical Allele Identifier: CA1435771649

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301681G= , CM000666.2:g.6301681G=	GRCh38
NC_000004.11:g.6303408G= , CM000666.1:g.6303408G=	GRCh37
NC_000004.10:g.6354309G=	NCBI36
NG_011700.1:g.36832G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1922G=	ENSP00000507852.1:p.Arg641=
ENST00000683395.1:c.1863G=
ENST00000684087.1:c.1886G=	ENSP00000506978.1:p.Arg629=
ENST00000506362.2:c.1637G=	ENSP00000424103.2:p.Arg546=
ENST00000673642.1:c.1545G=	ENSP00000501242.1:n.1545G=
ENST00000673991.1:c.1922G=	ENSP00000501033.1:p.Arg641=
ENST00000226760.5:c.1886G= MANE Select	ENSP00000226760.1:p.Arg629=
ENST00000503569.5:c.1886G=	ENSP00000423337.1:p.Arg629=
ENST00000507765.1:n.2071G=
NM_001145853.1:c.1886G=	NP_001139325.1:p.Arg629=
NM_006005.3:c.1886G= MANE Select	NP_005996.2:p.Arg629=
XM_017008586.1:c.1895G=	XP_016864075.1:p.Arg632=