Canonical Allele Identifier: CA1435769032

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6292048C= , CM000666.2:g.6292048C=	GRCh38
NC_000004.11:g.6293775C= , CM000666.1:g.6293775C=	GRCh37
NC_000004.10:g.6344676C=	NCBI36
NG_011700.1:g.27199C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.712+51C=	ENSP00000507852.1:n.712+51C=
ENST00000683395.1:c.689+51C=
ENST00000684087.1:c.712+51C=	ENSP00000506978.1:n.712+51C=
ENST00000506362.2:c.463+51C=	ENSP00000424103.2:n.463+51C=
ENST00000673642.1:c.511+51C=	ENSP00000501242.1:n.511+51C=
ENST00000673991.1:c.712+51C=	ENSP00000501033.1:n.712+51C=
ENST00000226760.5:c.712+51C= MANE Select	ENSP00000226760.1:n.712+51C=
ENST00000503569.5:c.712+51C=	ENSP00000423337.1:n.712+51C=
ENST00000506362.1:c.309+51C=
ENST00000507765.1:n.897+51C=
NM_001145853.1:c.712+51C=	NP_001139325.1:n.712+51C=
NM_006005.3:c.712+51C= MANE Select	NP_005996.2:n.712+51C=
XM_017008586.1:c.721+51C=	XP_016864075.1:n.721+51C=