Canonical Allele Identifier: CA1435772803

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301166G= , CM000666.2:g.6301166G=	GRCh38
NC_000004.11:g.6302893G= , CM000666.1:g.6302893G=	GRCh37
NC_000004.10:g.6353794G=	NCBI36
NG_011700.1:g.36317G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006005.3:c.1371G= MANE Select	NP_005996.2:p.Arg457=
ENST00000226760.5:c.1371G= MANE Select	ENSP00000226760.1:p.Arg457=
NM_001145853.1:c.1371G=	NP_001139325.1:p.Arg457=
ENST00000503569.5:c.1371G=	ENSP00000423337.1:p.Arg457=
ENST00000506362.2:c.1122G=	ENSP00000424103.2:p.Arg374=
ENST00000507765.1:n.1556G=
ENST00000673642.1:c.1030G=	ENSP00000501242.1:p.Gly344=
ENST00000673991.1:c.1407G=	ENSP00000501033.1:p.Arg469=
ENST00000682275.1:c.1407G=	ENSP00000507852.1:p.Arg469=
ENST00000683395.1:c.1348G=
ENST00000684087.1:c.1371G=	ENSP00000506978.1:p.Arg457=
XM_017008586.1:c.1380G=	XP_016864075.1:p.Arg460=