Canonical Allele Identifier: CA1435772358

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302122A= , CM000666.2:g.6302122A=	GRCh38
NC_000004.11:g.6303849A= , CM000666.1:g.6303849A=	GRCh37
NC_000004.10:g.6354750A=	NCBI36
NG_011700.1:g.37273A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2363A=	ENSP00000507852.1:p.Glu788=
ENST00000683395.1:c.2304A=
ENST00000684087.1:c.2327A=	ENSP00000506978.1:p.Glu776=
ENST00000506362.2:c.2078A=	ENSP00000424103.2:p.Glu693=
ENST00000673642.1:c.1986A=	ENSP00000501242.1:n.1986A=
ENST00000673991.1:c.2363A=	ENSP00000501033.1:p.Glu788=
ENST00000226760.5:c.2327A= MANE Select	ENSP00000226760.1:p.Glu776=
ENST00000503569.5:c.2327A=	ENSP00000423337.1:p.Glu776=
ENST00000507765.1:n.2512A=
NM_001145853.1:c.2327A=	NP_001139325.1:p.Glu776=
NM_006005.3:c.2327A= MANE Select	NP_005996.2:p.Glu776=
XM_017008586.1:c.2336A=	XP_016864075.1:p.Glu779=