Canonical Allele Identifier: CA1435768998

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6292005C= , CM000666.2:g.6292005C=	GRCh38
NC_000004.11:g.6293732C= , CM000666.1:g.6293732C=	GRCh37
NC_000004.10:g.6344633C=	NCBI36
NG_011700.1:g.27156C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.712+8C=	ENSP00000507852.1:n.712+8C=
ENST00000683395.1:c.689+8C=
ENST00000684087.1:c.712+8C=	ENSP00000506978.1:n.712+8C=
ENST00000506362.2:c.463+8C=	ENSP00000424103.2:n.463+8C=
ENST00000673642.1:c.511+8C=	ENSP00000501242.1:n.511+8C=
ENST00000673991.1:c.712+8C=	ENSP00000501033.1:n.712+8C=
ENST00000226760.5:c.712+8C= MANE Select	ENSP00000226760.1:n.712+8C=
ENST00000503569.5:c.712+8C=	ENSP00000423337.1:n.712+8C=
ENST00000506362.1:c.309+8C=
ENST00000507765.1:n.897+8C=
NM_001145853.1:c.712+8C=	NP_001139325.1:n.712+8C=
NM_006005.3:c.712+8C= MANE Select	NP_005996.2:n.712+8C=
XM_017008586.1:c.721+8C=	XP_016864075.1:n.721+8C=