Canonical Allele Identifier: CA1435765675

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6288259T= , CM000666.2:g.6288259T=	GRCh38
NC_000004.11:g.6289986T= , CM000666.1:g.6289986T=	GRCh37
NC_000004.10:g.6340887T=	NCBI36
NG_011700.1:g.23410T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.316-728T=	ENSP00000507852.1:n.316-728T=
ENST00000683395.1:c.306-728T=
ENST00000684054.1:c.316-728T=	ENSP00000507120.1:n.316-728T=
ENST00000684087.1:c.316-728T=	ENSP00000506978.1:n.316-728T=
ENST00000684700.1:c.316-728T=	ENSP00000507806.1:n.316-728T=
ENST00000506362.2:c.67-728T=	ENSP00000424103.2:n.67-728T=
ENST00000673642.1:c.115-728T=	ENSP00000501242.1:n.115-728T=
ENST00000673991.1:c.316-728T=	ENSP00000501033.1:n.316-728T=
ENST00000674051.1:c.190-728T=	ENSP00000501083.1:n.190-728T=
ENST00000226760.5:c.316-728T= MANE Select	ENSP00000226760.1:n.316-728T=
ENST00000503569.5:c.316-728T=	ENSP00000423337.1:n.316-728T=
NM_001145853.1:c.316-728T=	NP_001139325.1:n.316-728T=
NM_006005.3:c.316-728T= MANE Select	NP_005996.2:n.316-728T=
XM_017008586.1:c.325-728T=	XP_016864075.1:n.325-728T=