Canonical Allele Identifier: CA979334448
Gene: WWOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78108410_78108411insTTTTTTT , CM000678.2:g.78108410_78108411insTTTTTTT GRCh38
NC_000016.9:g.78142307_78142308insTTTTTTT , CM000678.1:g.78142307_78142308insTTTTTTT GRCh37
NC_000016.8:g.76699808_76699809insTTTTTTT NCBI36
NG_011698.1:g.13757_13758insTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.108-13_108-12insTTTTTTT ENSP00000485925.2:n.108-13_108-12insTTTTTTT
ENST00000682609.1:n.435-13_435-12insTTTTTTT
ENST00000683286.1:n.435-13_435-12insTTTTTTT
ENST00000683929.1:c.108-13_108-12insTTTTTTT ENSP00000507689.1:n.108-13_108-12insTTTTTTT
ENST00000684070.1:n.437-1368_437-1367insTTTTTTT
ENST00000684381.1:n.435-13_435-12insTTTTTTT
ENST00000684452.1:n.435-13_435-12insTTTTTTT
ENST00000684632.1:n.487-13_487-12insTTTTTTT
ENST00000566780.6:c.108-13_108-12insTTTTTTT MANE Select ENSP00000457230.1:n.108-13_108-12insTTTTTTT
ENST00000355860.7:c.108-13_108-12insTTTTTTT ENSP00000348119.3:n.108-13_108-12insTTTTTTT
ENST00000402655.6:c.108-13_108-12insTTTTTTT ENSP00000384238.2:n.108-13_108-12insTTTTTTT
ENST00000406884.6:c.108-13_108-12insTTTTTTT ENSP00000384495.2:n.108-13_108-12insTTTTTTT
ENST00000408984.7:c.108-13_108-12insTTTTTTT ENSP00000386161.3:n.108-13_108-12insTTTTTTT
ENST00000539474.6:c.108-13_108-12insTTTTTTT ENSP00000445210.2:n.108-13_108-12insTTTTTTT
ENST00000561846.5:n.152-13_152-12insTTTTTTT
ENST00000562214.5:n.231-13_231-12insTTTTTTT
ENST00000563358.5:n.215-13_215-12insTTTTTTT
ENST00000565562.5:n.153-13_153-12insTTTTTTT
ENST00000566662.5:c.108-1368_108-1367insTTTTTTT ENSP00000454331.1:n.108-1368_108-1367insTTTTTTT
ENST00000566780.5:c.108-13_108-12insTTTTTTT ENSP00000457230.1:n.108-13_108-12insTTTTTTT
ENST00000569332.5:c.108-1368_108-1367insTTTTTTT ENSP00000454788.1:n.108-1368_108-1367insTTTTTTT
ENST00000627394.2:c.108-1368_108-1367insTTTTTTT ENSP00000485925.1:n.108-1368_108-1367insTTTTTTT
NM_001291997.1:c.-167-1368_-167-1367insTTTTTTT NP_001278926.1:n.-167-1368_-167-1367insTTTTTTT
NM_016373.3:c.108-13_108-12insTTTTTTT NP_057457.1:n.108-13_108-12insTTTTTTT
NM_130791.3:c.108-13_108-12insTTTTTTT NP_570607.1:n.108-13_108-12insTTTTTTT
NR_120436.1:n.588-13_588-12insTTTTTTT
XM_006721195.2:c.108-13_108-12insTTTTTTT XP_006721258.1:n.108-13_108-12insTTTTTTT
XM_011523100.1:c.108-13_108-12insTTTTTTT XP_011521402.1:n.108-13_108-12insTTTTTTT
XM_011523101.1:c.108-13_108-12insTTTTTTT XP_011521403.1:n.108-13_108-12insTTTTTTT
XM_011523102.1:c.108-13_108-12insTTTTTTT XP_011521404.1:n.108-13_108-12insTTTTTTT
XM_011523103.1:c.108-13_108-12insTTTTTTT XP_011521405.1:n.108-13_108-12insTTTTTTT
XM_011523104.1:c.108-13_108-12insTTTTTTT XP_011521406.1:n.108-13_108-12insTTTTTTT
XM_011523105.1:c.108-13_108-12insTTTTTTT XP_011521407.1:n.108-13_108-12insTTTTTTT
XM_011523101.3:c.108-13_108-12insTTTTTTT XP_011521403.1:n.108-13_108-12insTTTTTTT
XM_011523103.3:c.108-13_108-12insTTTTTTT XP_011521405.1:n.108-13_108-12insTTTTTTT
XM_011523104.3:c.108-13_108-12insTTTTTTT XP_011521406.1:n.108-13_108-12insTTTTTTT
XM_011523105.3:c.108-13_108-12insTTTTTTT XP_011521407.1:n.108-13_108-12insTTTTTTT
XM_017023278.2:c.108-13_108-12insTTTTTTT XP_016878767.1:n.108-13_108-12insTTTTTTT
NM_016373.4:c.108-13_108-12insTTTTTTT MANE Select NP_057457.1:n.108-13_108-12insTTTTTTT
NM_001291997.2:c.-167-1368_-167-1367insTTTTTTT NP_001278926.1:n.-167-1368_-167-1367insTTTTTTT
NM_130791.4:c.108-13_108-12insTTTTTTT NP_570607.1:n.108-13_108-12insTTTTTTT
NR_120436.2:n.347-13_347-12insTTTTTTT
NM_130791.5:c.108-13_108-12insTTTTTTT NP_570607.1:n.108-13_108-12insTTTTTTT
NR_120436.3:n.347-13_347-12insTTTTTTT