Canonical Allele Identifier: CA1435768837

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291720G= , CM000666.2:g.6291720G=	GRCh38
NC_000004.11:g.6293447G= , CM000666.1:g.6293447G=	GRCh37
NC_000004.10:g.6344348G=	NCBI36
NG_011700.1:g.26871G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.632-197G=	ENSP00000507852.1:n.632-197G=
ENST00000683395.1:c.609-197G=
ENST00000684087.1:c.632-197G=	ENSP00000506978.1:n.632-197G=
ENST00000506362.2:c.383-197G=	ENSP00000424103.2:n.383-197G=
ENST00000673642.1:c.431-197G=	ENSP00000501242.1:n.431-197G=
ENST00000673991.1:c.632-197G=	ENSP00000501033.1:n.632-197G=
ENST00000226760.5:c.632-197G= MANE Select	ENSP00000226760.1:n.632-197G=
ENST00000503569.5:c.632-197G=	ENSP00000423337.1:n.632-197G=
ENST00000506362.1:c.229-197G=
ENST00000507765.1:n.817-197G=
NM_001145853.1:c.632-197G=	NP_001139325.1:n.632-197G=
NM_006005.3:c.632-197G= MANE Select	NP_005996.2:n.632-197G=
XM_017008586.1:c.641-197G=	XP_016864075.1:n.641-197G=