Canonical Allele Identifier: CA1435772575

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302289C= , CM000666.2:g.6302289C=	GRCh38
NC_000004.11:g.6304016C= , CM000666.1:g.6304016C=	GRCh37
NC_000004.10:g.6354917C=	NCBI36
NG_011700.1:g.37440C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2530C=	ENSP00000507852.1:p.Arg844=
ENST00000683395.1:c.2471C=
ENST00000684087.1:c.2494C=	ENSP00000506978.1:p.Arg832=
ENST00000506362.2:c.2245C=	ENSP00000424103.2:p.Arg749=
ENST00000673991.1:c.2530C=	ENSP00000501033.1:p.Arg844=
ENST00000226760.5:c.2494C= MANE Select	ENSP00000226760.1:p.Arg832=
ENST00000503569.5:c.2494C=	ENSP00000423337.1:p.Arg832=
ENST00000507765.1:n.2679C=
NM_001145853.1:c.2494C=	NP_001139325.1:p.Arg832=
NM_006005.3:c.2494C= MANE Select	NP_005996.2:p.Arg832=
XM_017008586.1:c.2503C=	XP_016864075.1:p.Arg835=