Canonical Allele Identifier: CA2235117210

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78424869G= , CM000678.2:g.78424869G=	GRCh38
NC_000016.9:g.78458766G= , CM000678.1:g.78458766G=	GRCh37
NC_000016.8:g.77016267G=	NCBI36
NG_011698.1:g.330216G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.606-1G= MANE Select	NP_057457.1:n.606-1G=
ENST00000566780.6:c.606-1G= MANE Select	ENSP00000457230.1:n.606-1G=
NM_001291997.1:c.267-1G=	NP_001278926.1:n.267-1G=
NM_001291997.2:c.267-1G=	NP_001278926.1:n.267-1G=
NM_016373.3:c.606-1G=	NP_057457.1:n.606-1G=
ENST00000402655.6:c.409+309715G=	ENSP00000384238.2:n.409+309715G=
ENST00000406884.6:c.516+260580G=	ENSP00000384495.2:n.516+260580G=
ENST00000408984.7:c.606-1G=	ENSP00000386161.3:n.606-1G=
ENST00000539474.6:c.409+309715G=	ENSP00000445210.2:n.409+309715G=
ENST00000562639.5:n.294-1G=
ENST00000566662.5:c.*224-1G=	ENSP00000454331.1:n.*224-1G=
ENST00000566780.5:c.606-1G=	ENSP00000457230.1:n.606-1G=
ENST00000569332.5:c.*403-1G=	ENSP00000454788.1:n.*403-1G=
ENST00000627394.3:c.606-1G=	ENSP00000485925.2:n.606-1G=
ENST00000683929.1:c.606-1G=	ENSP00000507689.1:n.606-1G=
ENST00000684632.1:n.985-1G=
XM_006721195.2:c.606-1G=	XP_006721258.1:n.606-1G=
XM_011523100.1:c.606-1G=	XP_011521402.1:n.606-1G=
XM_011523101.1:c.606-1G=	XP_011521403.1:n.606-1G=
XM_011523101.3:c.606-1G=	XP_011521403.1:n.606-1G=
XM_011523102.1:c.606-1G=	XP_011521404.1:n.606-1G=
XM_011523103.1:c.606-1G=	XP_011521405.1:n.606-1G=
XM_011523103.3:c.606-1G=	XP_011521405.1:n.606-1G=
XM_011523104.1:c.606-1G=	XP_011521406.1:n.606-1G=
XM_011523104.3:c.606-1G=	XP_011521406.1:n.606-1G=
XR_933765.1:n.3806+5557C=