Canonical Allele Identifier: CA8183162
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 383820
dbSNP Id: rs114755364

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78115077C>G , CM000678.2:g.78115077C>G GRCh38
NC_000016.9:g.78148974C>G , CM000678.1:g.78148974C>G GRCh37
NC_000016.8:g.76706475C>G NCBI36
NG_011698.1:g.20424C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.332C>G ENSP00000485925.2:p.Thr111Ser
ENST00000682609.1:n.659C>G
ENST00000683286.1:n.659C>G
ENST00000683929.1:c.332C>G ENSP00000507689.1:p.Thr111Ser
ENST00000684070.1:n.596C>G
ENST00000684381.1:n.659C>G
ENST00000684452.1:n.659C>G
ENST00000684632.1:n.711C>G
ENST00000566780.6:c.332C>G MANE Select ENSP00000457230.1:p.Thr111Ser
ENST00000355860.7:c.332C>G ENSP00000348119.3:p.Thr111Ser
ENST00000402655.6:c.332C>G ENSP00000384238.2:p.Thr111Ser
ENST00000406884.6:c.332C>G ENSP00000384495.2:p.Thr111Ser
ENST00000408984.7:c.332C>G ENSP00000386161.3:p.Thr111Ser
ENST00000539474.6:c.332C>G ENSP00000445210.2:p.Thr111Ser
ENST00000561846.5:n.376C>G
ENST00000562214.5:n.455C>G
ENST00000563358.5:n.439C>G
ENST00000566662.5:c.*27+5242C>G ENSP00000454331.1:n.*27+5242C>G
ENST00000566780.5:c.332C>G ENSP00000457230.1:p.Thr111Ser
ENST00000569332.5:c.*129C>G ENSP00000454788.1:n.*129C>G
ENST00000627394.2:c.*129C>G ENSP00000485925.1:n.*129C>G
NM_001291997.1:c.-8C>G NP_001278926.1:n.-8C>G
NM_016373.3:c.332C>G NP_057457.1:p.Thr111Ser
NM_130791.3:c.332C>G NP_570607.1:p.Thr111Ser
NR_120436.1:n.812C>G
XM_006721195.2:c.332C>G XP_006721258.1:p.Thr111Ser
XM_011523100.1:c.332C>G XP_011521402.1:p.Thr111Ser
XM_011523101.1:c.332C>G XP_011521403.1:p.Thr111Ser
XM_011523102.1:c.332C>G XP_011521404.1:p.Thr111Ser
XM_011523103.1:c.332C>G XP_011521405.1:p.Thr111Ser
XM_011523104.1:c.332C>G XP_011521406.1:p.Thr111Ser
XM_011523105.1:c.332C>G XP_011521407.1:p.Thr111Ser
XM_011523101.3:c.332C>G XP_011521403.1:p.Thr111Ser
XM_011523103.3:c.332C>G XP_011521405.1:p.Thr111Ser
XM_011523104.3:c.332C>G XP_011521406.1:p.Thr111Ser
XM_011523105.3:c.332C>G XP_011521407.1:p.Thr111Ser
XM_017023278.2:c.332C>G XP_016878767.1:p.Thr111Ser
NM_016373.4:c.332C>G MANE Select NP_057457.1:p.Thr111Ser
NM_001291997.2:c.-8C>G NP_001278926.1:n.-8C>G
NM_130791.4:c.332C>G NP_570607.1:p.Thr111Ser
NR_120436.2:n.571C>G
NM_130791.5:c.332C>G NP_570607.1:p.Thr111Ser
NR_120436.3:n.571C>G