Canonical Allele Identifier: CA1435768759

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291563A= , CM000666.2:g.6291563A=	GRCh38
NC_000004.11:g.6293290A= , CM000666.1:g.6293290A=	GRCh37
NC_000004.10:g.6344191A=	NCBI36
NG_011700.1:g.26714A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.631+196A=	ENSP00000507852.1:n.631+196A=
ENST00000683395.1:c.608+209A=
ENST00000684087.1:c.631+196A=	ENSP00000506978.1:n.631+196A=
ENST00000684700.1:c.*122A=	ENSP00000507806.1:n.*122A=
ENST00000506362.2:c.382+196A=	ENSP00000424103.2:n.382+196A=
ENST00000673642.1:c.430+196A=	ENSP00000501242.1:n.430+196A=
ENST00000673991.1:c.631+196A=	ENSP00000501033.1:n.631+196A=
ENST00000226760.5:c.631+196A= MANE Select	ENSP00000226760.1:n.631+196A=
ENST00000503569.5:c.631+196A=	ENSP00000423337.1:n.631+196A=
ENST00000506362.1:c.228+196A=
ENST00000507765.1:n.816+196A=
NM_001145853.1:c.631+196A=	NP_001139325.1:n.631+196A=
NM_006005.3:c.631+196A= MANE Select	NP_005996.2:n.631+196A=
XM_017008586.1:c.640+196A=	XP_016864075.1:n.640+196A=