Canonical Allele Identifier: CA1435773706

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301478C= , CM000666.2:g.6301478C=	GRCh38
NC_000004.11:g.6303205C= , CM000666.1:g.6303205C=	GRCh37
NC_000004.10:g.6354106C=	NCBI36
NG_011700.1:g.36629C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1719C=	ENSP00000507852.1:p.Ile573=
ENST00000683395.1:c.1660C=
ENST00000684087.1:c.1683C=	ENSP00000506978.1:p.Ile561=
ENST00000506362.2:c.1434C=	ENSP00000424103.2:p.Ile478=
ENST00000673642.1:c.1342C=	ENSP00000501242.1:n.1342C=
ENST00000673991.1:c.1719C=	ENSP00000501033.1:p.Ile573=
ENST00000226760.5:c.1683C= MANE Select	ENSP00000226760.1:p.Ile561=
ENST00000503569.5:c.1683C=	ENSP00000423337.1:p.Ile561=
ENST00000507765.1:n.1868C=
NM_001145853.1:c.1683C=	NP_001139325.1:p.Ile561=
NM_006005.3:c.1683C= MANE Select	NP_005996.2:p.Ile561=
XM_017008586.1:c.1692C=	XP_016864075.1:p.Ile564=