Canonical Allele Identifier: CA1435768638

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291350G= , CM000666.2:g.6291350G=	GRCh38
NC_000004.11:g.6293077G= , CM000666.1:g.6293077G=	GRCh37
NC_000004.10:g.6343978G=	NCBI36
NG_011700.1:g.26501G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.614G=	ENSP00000507852.1:p.Gly205=
ENST00000683395.1:c.604G=
ENST00000684087.1:c.614G=	ENSP00000506978.1:p.Gly205=
ENST00000684700.1:c.614G=	ENSP00000507806.1:p.Gly205=
ENST00000506362.2:c.365G=	ENSP00000424103.2:p.Gly122=
ENST00000673642.1:c.413G=	ENSP00000501242.1:p.Gly138=
ENST00000673991.1:c.614G=	ENSP00000501033.1:p.Gly205=
ENST00000226760.5:c.614G= MANE Select	ENSP00000226760.1:p.Gly205=
ENST00000503569.5:c.614G=	ENSP00000423337.1:p.Gly205=
ENST00000506362.1:c.211G=
ENST00000507765.1:n.799G=
NM_001145853.1:c.614G=	NP_001139325.1:p.Gly205=
NM_006005.3:c.614G= MANE Select	NP_005996.2:p.Gly205=
XM_017008586.1:c.623G=	XP_016864075.1:p.Gly208=