Canonical Allele Identifier: CA1435773808

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301511C= , CM000666.2:g.6301511C=	GRCh38
NC_000004.11:g.6303238C= , CM000666.1:g.6303238C=	GRCh37
NC_000004.10:g.6354139C=	NCBI36
NG_011700.1:g.36662C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1752C=	ENSP00000507852.1:p.Ile584=
ENST00000683395.1:c.1693C=
ENST00000684087.1:c.1716C=	ENSP00000506978.1:p.Ile572=
ENST00000506362.2:c.1467C=	ENSP00000424103.2:p.Ile489=
ENST00000673642.1:c.1375C=	ENSP00000501242.1:n.1375C=
ENST00000673991.1:c.1752C=	ENSP00000501033.1:p.Ile584=
ENST00000226760.5:c.1716C= MANE Select	ENSP00000226760.1:p.Ile572=
ENST00000503569.5:c.1716C=	ENSP00000423337.1:p.Ile572=
ENST00000507765.1:n.1901C=
NM_001145853.1:c.1716C=	NP_001139325.1:p.Ile572=
NM_006005.3:c.1716C= MANE Select	NP_005996.2:p.Ile572=
XM_017008586.1:c.1725C=	XP_016864075.1:p.Ile575=