Canonical Allele Identifier: CA1435768260

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6290668G= , CM000666.2:g.6290668G=	GRCh38
NC_000004.11:g.6292395G= , CM000666.1:g.6292395G=	GRCh37
NC_000004.10:g.6343296G=	NCBI36
NG_011700.1:g.25819G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.461-529G=	ENSP00000507852.1:n.461-529G=
ENST00000683395.1:c.451-529G=
ENST00000684087.1:c.461-529G=	ENSP00000506978.1:n.461-529G=
ENST00000684700.1:c.461-529G=	ENSP00000507806.1:n.461-529G=
ENST00000506362.2:c.212-529G=	ENSP00000424103.2:n.212-529G=
ENST00000673642.1:c.260-529G=	ENSP00000501242.1:n.260-529G=
ENST00000673991.1:c.461-529G=	ENSP00000501033.1:n.461-529G=
ENST00000674051.1:c.335-529G=	ENSP00000501083.1:n.335-529G=
ENST00000226760.5:c.461-529G= MANE Select	ENSP00000226760.1:n.461-529G=
ENST00000503569.5:c.461-529G=	ENSP00000423337.1:n.461-529G=
ENST00000506362.1:c.58-529G=
ENST00000507765.1:n.646-529G=
NM_001145853.1:c.461-529G=	NP_001139325.1:n.461-529G=
NM_006005.3:c.461-529G= MANE Select	NP_005996.2:n.461-529G=
XM_017008586.1:c.470-529G=	XP_016864075.1:n.470-529G=