Canonical Allele Identifier: CA1435772249

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302040A= , CM000666.2:g.6302040A=	GRCh38
NC_000004.11:g.6303767A= , CM000666.1:g.6303767A=	GRCh37
NC_000004.10:g.6354668A=	NCBI36
NG_011700.1:g.37191A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2281A=	ENSP00000507852.1:p.Thr761=
ENST00000683395.1:c.2222A=
ENST00000684087.1:c.2245A=	ENSP00000506978.1:p.Thr749=
ENST00000506362.2:c.1996A=	ENSP00000424103.2:p.Thr666=
ENST00000673642.1:c.1904A=	ENSP00000501242.1:n.1904A=
ENST00000673991.1:c.2281A=	ENSP00000501033.1:p.Thr761=
ENST00000226760.5:c.2245A= MANE Select	ENSP00000226760.1:p.Thr749=
ENST00000503569.5:c.2245A=	ENSP00000423337.1:p.Thr749=
ENST00000507765.1:n.2430A=
NM_001145853.1:c.2245A=	NP_001139325.1:p.Thr749=
NM_006005.3:c.2245A= MANE Select	NP_005996.2:p.Thr749=
XM_017008586.1:c.2254A=	XP_016864075.1:p.Thr752=