Canonical Allele Identifier: CA1435772168

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301990G= , CM000666.2:g.6301990G=	GRCh38
NC_000004.11:g.6303717G= , CM000666.1:g.6303717G=	GRCh37
NC_000004.10:g.6354618G=	NCBI36
NG_011700.1:g.37141G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006005.3:c.2195G= MANE Select	NP_005996.2:p.Arg732=
ENST00000226760.5:c.2195G= MANE Select	ENSP00000226760.1:p.Arg732=
NM_001145853.1:c.2195G=	NP_001139325.1:p.Arg732=
ENST00000503569.5:c.2195G=	ENSP00000423337.1:p.Arg732=
ENST00000506362.2:c.1946G=	ENSP00000424103.2:p.Arg649=
ENST00000507765.1:n.2380G=
ENST00000673642.1:c.1854G=	ENSP00000501242.1:n.1854G=
ENST00000673991.1:c.2231G=	ENSP00000501033.1:p.Arg744=
ENST00000682275.1:c.2231G=	ENSP00000507852.1:p.Arg744=
ENST00000683395.1:c.2172G=
ENST00000684087.1:c.2195G=	ENSP00000506978.1:p.Arg732=
XM_017008586.1:c.2204G=	XP_016864075.1:p.Arg735=