Canonical Allele Identifier: CA1435772479

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302210G= , CM000666.2:g.6302210G=	GRCh38
NC_000004.11:g.6303937G= , CM000666.1:g.6303937G=	GRCh37
NC_000004.10:g.6354838G=	NCBI36
NG_011700.1:g.37361G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2451G=	ENSP00000507852.1:p.Arg817=
ENST00000683395.1:c.2392G=
ENST00000684087.1:c.2415G=	ENSP00000506978.1:p.Arg805=
ENST00000506362.2:c.2166G=	ENSP00000424103.2:p.Arg722=
ENST00000673991.1:c.2451G=	ENSP00000501033.1:p.Arg817=
ENST00000226760.5:c.2415G= MANE Select	ENSP00000226760.1:p.Arg805=
ENST00000503569.5:c.2415G=	ENSP00000423337.1:p.Arg805=
ENST00000507765.1:n.2600G=
NM_001145853.1:c.2415G=	NP_001139325.1:p.Arg805=
NM_006005.3:c.2415G= MANE Select	NP_005996.2:p.Arg805=
XM_017008586.1:c.2424G=	XP_016864075.1:p.Arg808=