Canonical Allele Identifier: CA3217832157

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432614G= , CM000678.2:g.78432614G=	GRCh38
NC_000016.9:g.78466511G= , CM000678.1:g.78466511G=	GRCh37
NC_000016.8:g.77024012G=	NCBI36
NG_011698.1:g.337961G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.918G= MANE Select	NP_057457.1:p.Glu306=
ENST00000566780.6:c.918G= MANE Select	ENSP00000457230.1:p.Glu306=
NM_001291997.1:c.579G=	NP_001278926.1:p.Glu193=
NM_001291997.2:c.579G=	NP_001278926.1:p.Glu193=
NM_016373.3:c.918G=	NP_057457.1:p.Glu306=
ENST00000402655.6:c.409+317460G=	ENSP00000384238.2:n.409+317460G=
ENST00000406884.6:c.516+268325G=	ENSP00000384495.2:n.516+268325G=
ENST00000408984.7:c.918G=	ENSP00000386161.3:p.Glu306=
ENST00000539474.6:c.409+317460G=	ENSP00000445210.2:n.409+317460G=
ENST00000566780.5:c.918G=	ENSP00000457230.1:p.Glu306=
ENST00000569332.5:c.*715G=	ENSP00000454788.1:n.*715G=
ENST00000620008.1:c.312G=	ENSP00000482648.1:p.Glu104=
ENST00000627394.3:c.918G=	ENSP00000485925.2:p.Glu306=
ENST00000683929.1:c.918G=	ENSP00000507689.1:p.Glu306=
ENST00000684632.1:n.1297G=
XM_006721195.2:c.918G=	XP_006721258.1:p.Glu306=
XM_011523100.1:c.918G=	XP_011521402.1:p.Glu306=
XM_011523101.1:c.918G=	XP_011521403.1:p.Glu306=
XM_011523101.3:c.918G=	XP_011521403.1:p.Glu306=
XM_011523102.1:c.918G=	XP_011521404.1:p.Glu306=
XM_011523103.1:c.918G=	XP_011521405.1:p.Glu306=
XM_011523103.3:c.918G=	XP_011521405.1:p.Glu306=
XM_011523104.1:c.918G=	XP_011521406.1:p.Glu306=
XM_011523104.3:c.918G=	XP_011521406.1:p.Glu306=
XR_933765.1:n.3418+1706C=