Canonical Allele Identifier: CA2235147073

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78536028G= , CM000678.2:g.78536028G=	GRCh38
NC_000016.9:g.78569925G= , CM000678.1:g.78569925G=	GRCh37
NC_000016.8:g.77127426G=	NCBI36
NG_011698.1:g.441375G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.1152+186G=	ENSP00000485925.2:n.1152+186G=
ENST00000683929.1:c.1056+103276G=	ENSP00000507689.1:n.1056+103276G=
ENST00000684632.1:n.1436-99819G=
ENST00000566780.6:c.1056+103276G= MANE Select	ENSP00000457230.1:n.1056+103276G=
ENST00000402655.6:c.409+420874G=	ENSP00000384238.2:n.409+420874G=
ENST00000406884.6:c.516+371739G=	ENSP00000384495.2:n.516+371739G=
ENST00000408984.7:c.1056+103276G=	ENSP00000386161.3:n.1056+103276G=
ENST00000539474.6:c.410-220912G=	ENSP00000445210.2:n.410-220912G=
ENST00000566780.5:c.1056+103276G=	ENSP00000457230.1:n.1056+103276G=
ENST00000569332.5:c.*853+103276G=	ENSP00000454788.1:n.*853+103276G=
NM_001291997.1:c.717+103276G=	NP_001278926.1:n.717+103276G=
NM_016373.3:c.1056+103276G=	NP_057457.1:n.1056+103276G=
XM_011523100.1:c.1152+186G=	XP_011521402.1:n.1152+186G=
XM_011523101.1:c.1057-38031G=	XP_011521403.1:n.1057-38031G=
XM_011523103.1:c.1056+103276G=	XP_011521405.1:n.1056+103276G=
XM_011523101.3:c.1057-38031G=	XP_011521403.1:n.1057-38031G=
XM_011523103.3:c.1056+103276G=	XP_011521405.1:n.1056+103276G=
XM_017023279.1:c.142+186G=	XP_016878768.1:n.142+186G=
NM_016373.4:c.1056+103276G= MANE Select	NP_057457.1:n.1056+103276G=
NM_001291997.2:c.717+103276G=	NP_001278926.1:n.717+103276G=