Canonical Allele Identifier: CA1435772453

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302187G= , CM000666.2:g.6302187G=	GRCh38
NC_000004.11:g.6303914G= , CM000666.1:g.6303914G=	GRCh37
NC_000004.10:g.6354815G=	NCBI36
NG_011700.1:g.37338G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.2428G=	ENSP00000507852.1:p.Val810=
ENST00000683395.1:c.2369G=
ENST00000684087.1:c.2392G=	ENSP00000506978.1:p.Val798=
ENST00000506362.2:c.2143G=	ENSP00000424103.2:p.Val715=
ENST00000673991.1:c.2428G=	ENSP00000501033.1:p.Val810=
ENST00000226760.5:c.2392G= MANE Select	ENSP00000226760.1:p.Val798=
ENST00000503569.5:c.2392G=	ENSP00000423337.1:p.Val798=
ENST00000507765.1:n.2577G=
NM_001145853.1:c.2392G=	NP_001139325.1:p.Val798=
NM_006005.3:c.2392G= MANE Select	NP_005996.2:p.Val798=
XM_017008586.1:c.2401G=	XP_016864075.1:p.Val801=