Canonical Allele Identifier: CA1435773172

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302760G= , CM000666.2:g.6302760G=	GRCh38
NC_000004.11:g.6304487G= , CM000666.1:g.6304487G=	GRCh37
NC_000004.10:g.6355388G=	NCBI36
NG_011700.1:g.37911G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*292G=	ENSP00000507852.1:n.*292G=
ENST00000683395.1:c.2942G=
ENST00000684087.1:c.*292G=	ENSP00000506978.1:n.*292G=
ENST00000506362.2:c.*292G=	ENSP00000424103.2:n.*292G=
ENST00000673991.1:c.*292G=	ENSP00000501033.1:n.*292G=
ENST00000226760.5:c.*292G= MANE Select	ENSP00000226760.1:n.*292G=
ENST00000503569.5:c.*292G=	ENSP00000423337.1:n.*292G=
ENST00000507765.1:n.3150G=
NM_001145853.1:c.*292G=	NP_001139325.1:n.*292G=
NM_006005.3:c.*292G= MANE Select	NP_005996.2:n.*292G=
XM_017008586.1:c.*292G=	XP_016864075.1:n.*292G=