Canonical Allele Identifier: CA1435771718

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301718G= , CM000666.2:g.6301718G=	GRCh38
NC_000004.11:g.6303445G= , CM000666.1:g.6303445G=	GRCh37
NC_000004.10:g.6354346G=	NCBI36
NG_011700.1:g.36869G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1959G=	ENSP00000507852.1:p.Thr653=
ENST00000683395.1:c.1900G=
ENST00000684087.1:c.1923G=	ENSP00000506978.1:p.Thr641=
ENST00000506362.2:c.1674G=	ENSP00000424103.2:p.Thr558=
ENST00000673642.1:c.1582G=	ENSP00000501242.1:n.1582G=
ENST00000673991.1:c.1959G=	ENSP00000501033.1:p.Thr653=
ENST00000226760.5:c.1923G= MANE Select	ENSP00000226760.1:p.Thr641=
ENST00000503569.5:c.1923G=	ENSP00000423337.1:p.Thr641=
ENST00000507765.1:n.2108G=
NM_001145853.1:c.1923G=	NP_001139325.1:p.Thr641=
NM_006005.3:c.1923G= MANE Select	NP_005996.2:p.Thr641=
XM_017008586.1:c.1932G=	XP_016864075.1:p.Thr644=