Canonical Allele Identifier: CA1435754155

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6277727A= , CM000666.2:g.6277727A=	GRCh38
NC_000004.11:g.6279454A= , CM000666.1:g.6279454A=	GRCh37
NC_000004.10:g.6330355A=	NCBI36
NG_011700.1:g.12878A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506588.6:n.402+40A=
ENST00000682059.1:c.232+40A=	ENSP00000507988.1:n.232+40A=
ENST00000682275.1:c.232+40A=	ENSP00000507852.1:n.232+40A=
ENST00000683395.1:c.222+40A=
ENST00000684054.1:c.232+40A=	ENSP00000507120.1:n.232+40A=
ENST00000684087.1:c.232+40A=	ENSP00000506978.1:n.232+40A=
ENST00000684700.1:c.232+40A=	ENSP00000507806.1:n.232+40A=
ENST00000506362.2:c.-18+7713A=	ENSP00000424103.2:n.-18+7713A=
ENST00000673642.1:c.31+40A=	ENSP00000501242.1:n.31+40A=
ENST00000673991.1:c.232+40A=	ENSP00000501033.1:n.232+40A=
ENST00000674051.1:c.106+40A=	ENSP00000501083.1:n.106+40A=
ENST00000226760.5:c.232+40A= MANE Select	ENSP00000226760.1:n.232+40A=
ENST00000503569.5:c.232+40A=	ENSP00000423337.1:n.232+40A=
ENST00000506588.5:n.402+40A=
NM_001145853.1:c.232+40A=	NP_001139325.1:n.232+40A=
NM_006005.3:c.232+40A= MANE Select	NP_005996.2:n.232+40A=
XM_017008586.1:c.241+40A=	XP_016864075.1:n.241+40A=