Canonical Allele Identifier: CA1435771725

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301723T= , CM000666.2:g.6301723T=	GRCh38
NC_000004.11:g.6303450T= , CM000666.1:g.6303450T=	GRCh37
NC_000004.10:g.6354351T=	NCBI36
NG_011700.1:g.36874T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1964T=	ENSP00000507852.1:p.Ile655=
ENST00000683395.1:c.1905T=
ENST00000684087.1:c.1928T=	ENSP00000506978.1:p.Ile643=
ENST00000506362.2:c.1679T=	ENSP00000424103.2:p.Ile560=
ENST00000673642.1:c.1587T=	ENSP00000501242.1:n.1587T=
ENST00000673991.1:c.1964T=	ENSP00000501033.1:p.Ile655=
ENST00000226760.5:c.1928T= MANE Select	ENSP00000226760.1:p.Ile643=
ENST00000503569.5:c.1928T=	ENSP00000423337.1:p.Ile643=
ENST00000507765.1:n.2113T=
NM_001145853.1:c.1928T=	NP_001139325.1:p.Ile643=
NM_006005.3:c.1928T= MANE Select	NP_005996.2:p.Ile643=
XM_017008586.1:c.1937T=	XP_016864075.1:p.Ile646=