Canonical Allele Identifier: CA1435773581

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301441T= , CM000666.2:g.6301441T=	GRCh38
NC_000004.11:g.6303168T= , CM000666.1:g.6303168T=	GRCh37
NC_000004.10:g.6354069T=	NCBI36
NG_011700.1:g.36592T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1682T=	ENSP00000507852.1:p.Leu561=
ENST00000683395.1:c.1623T=
ENST00000684087.1:c.1646T=	ENSP00000506978.1:p.Leu549=
ENST00000506362.2:c.1397T=	ENSP00000424103.2:p.Leu466=
ENST00000673642.1:c.1305T=	ENSP00000501242.1:n.1305T=
ENST00000673991.1:c.1682T=	ENSP00000501033.1:p.Leu561=
ENST00000226760.5:c.1646T= MANE Select	ENSP00000226760.1:p.Leu549=
ENST00000503569.5:c.1646T=	ENSP00000423337.1:p.Leu549=
ENST00000507765.1:n.1831T=
NM_001145853.1:c.1646T=	NP_001139325.1:p.Leu549=
NM_006005.3:c.1646T= MANE Select	NP_005996.2:p.Leu549=
XM_017008586.1:c.1655T=	XP_016864075.1:p.Leu552=