Canonical Allele Identifier: CA2235072437
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78432393A= , CM000678.2:g.78432393A= GRCh38
NC_000016.9:g.78466290A= , CM000678.1:g.78466290A= GRCh37
NC_000016.8:g.77023791A= NCBI36
NG_011698.1:g.337740A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.792-95A= ENSP00000485925.2:n.792-95A=
ENST00000683929.1:c.792-95A= ENSP00000507689.1:n.792-95A=
ENST00000684632.1:n.1171-95A=
ENST00000566780.6:c.792-95A= MANE Select ENSP00000457230.1:n.792-95A=
ENST00000402655.6:c.409+317239A= ENSP00000384238.2:n.409+317239A=
ENST00000406884.6:c.516+268104A= ENSP00000384495.2:n.516+268104A=
ENST00000408984.7:c.792-95A= ENSP00000386161.3:n.792-95A=
ENST00000539474.6:c.409+317239A= ENSP00000445210.2:n.409+317239A=
ENST00000562639.5:n.480-95A=
ENST00000566780.5:c.792-95A= ENSP00000457230.1:n.792-95A=
ENST00000569332.5:c.*589-95A= ENSP00000454788.1:n.*589-95A=
ENST00000620008.1:c.186-95A= ENSP00000482648.1:n.186-95A=
NM_001291997.1:c.453-95A= NP_001278926.1:n.453-95A=
NM_016373.3:c.792-95A= NP_057457.1:n.792-95A=
XM_006721195.2:c.792-95A= XP_006721258.1:n.792-95A=
XM_011523100.1:c.792-95A= XP_011521402.1:n.792-95A=
XM_011523101.1:c.792-95A= XP_011521403.1:n.792-95A=
XM_011523102.1:c.792-95A= XP_011521404.1:n.792-95A=
XM_011523103.1:c.792-95A= XP_011521405.1:n.792-95A=
XM_011523104.1:c.792-95A= XP_011521406.1:n.792-95A=
XR_933765.1:n.3419-1580T=
XM_011523101.3:c.792-95A= XP_011521403.1:n.792-95A=
XM_011523103.3:c.792-95A= XP_011521405.1:n.792-95A=
XM_011523104.3:c.792-95A= XP_011521406.1:n.792-95A=
NM_016373.4:c.792-95A= MANE Select NP_057457.1:n.792-95A=
NM_001291997.2:c.453-95A= NP_001278926.1:n.453-95A=