Canonical Allele Identifier: CA1435773579

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301439G= , CM000666.2:g.6301439G=	GRCh38
NC_000004.11:g.6303166G= , CM000666.1:g.6303166G=	GRCh37
NC_000004.10:g.6354067G=	NCBI36
NG_011700.1:g.36590G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1680G=	ENSP00000507852.1:p.Leu560=
ENST00000683395.1:c.1621G=
ENST00000684087.1:c.1644G=	ENSP00000506978.1:p.Leu548=
ENST00000506362.2:c.1395G=	ENSP00000424103.2:p.Leu465=
ENST00000673642.1:c.1303G=	ENSP00000501242.1:n.1303G=
ENST00000673991.1:c.1680G=	ENSP00000501033.1:p.Leu560=
ENST00000226760.5:c.1644G= MANE Select	ENSP00000226760.1:p.Leu548=
ENST00000503569.5:c.1644G=	ENSP00000423337.1:p.Leu548=
ENST00000507765.1:n.1829G=
NM_001145853.1:c.1644G=	NP_001139325.1:p.Leu548=
NM_006005.3:c.1644G= MANE Select	NP_005996.2:p.Leu548=
XM_017008586.1:c.1653G=	XP_016864075.1:p.Leu551=