Canonical Allele Identifier: CA2740093425
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2940258
ClinVar RCV Id: RCV003797616

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099886_78099887delinsTA , CM000678.2:g.78099886_78099887delinsTA GRCh38
NC_000016.9:g.78133783_78133784delinsTA , CM000678.1:g.78133783_78133784delinsTA GRCh37
NC_000016.8:g.76691284_76691285delinsTA NCBI36
NG_011698.1:g.5233_5234delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.107+1_107+2delinsTA ENSP00000485925.2:n.107+1_107+2delinsTA
ENST00000682609.1:n.434+1_434+2delinsTA
ENST00000683286.1:n.434+1_434+2delinsTA
ENST00000683929.1:c.107+1_107+2delinsTA ENSP00000507689.1:n.107+1_107+2delinsTA
ENST00000684070.1:n.436+1_436+2delinsTA
ENST00000684381.1:n.434+1_434+2delinsTA
ENST00000684452.1:n.434+1_434+2delinsTA
ENST00000684632.1:n.486+1_486+2delinsTA
ENST00000566780.6:c.107+1_107+2delinsTA MANE Select ENSP00000457230.1:n.107+1_107+2delinsTA
ENST00000355860.7:c.107+1_107+2delinsTA ENSP00000348119.3:n.107+1_107+2delinsTA
ENST00000402655.6:c.107+1_107+2delinsTA ENSP00000384238.2:n.107+1_107+2delinsTA
ENST00000406884.6:c.107+1_107+2delinsTA ENSP00000384495.2:n.107+1_107+2delinsTA
ENST00000408984.7:c.107+1_107+2delinsTA ENSP00000386161.3:n.107+1_107+2delinsTA
ENST00000539474.6:c.107+1_107+2delinsTA ENSP00000445210.2:n.107+1_107+2delinsTA
ENST00000561846.5:n.151+1_151+2delinsTA
ENST00000562214.5:n.230+1_230+2delinsTA
ENST00000563358.5:n.101_102delinsTA
ENST00000565562.5:n.152+1_152+2delinsTA
ENST00000566662.5:c.107+1_107+2delinsTA ENSP00000454331.1:n.107+1_107+2delinsTA
ENST00000566780.5:c.107+1_107+2delinsTA ENSP00000457230.1:n.107+1_107+2delinsTA
ENST00000569332.5:c.107+1_107+2delinsTA ENSP00000454788.1:n.107+1_107+2delinsTA
ENST00000569818.1:c.108_109delinsTA ENSP00000454485.1:p.Lys36_Ter37delinsAsnLys
ENST00000627394.2:c.107+1_107+2delinsTA ENSP00000485925.1:n.107+1_107+2delinsTA
NM_001291997.1:c.-168+1_-168+2delinsTA NP_001278926.1:n.-168+1_-168+2delinsTA
NM_016373.3:c.107+1_107+2delinsTA NP_057457.1:n.107+1_107+2delinsTA
NM_130791.3:c.107+1_107+2delinsTA NP_570607.1:n.107+1_107+2delinsTA
NR_120435.1:n.474_475delinsTA
NR_120436.1:n.474_475delinsTA
XM_006721195.2:c.107+1_107+2delinsTA XP_006721258.1:n.107+1_107+2delinsTA
XM_011523100.1:c.107+1_107+2delinsTA XP_011521402.1:n.107+1_107+2delinsTA
XM_011523101.1:c.107+1_107+2delinsTA XP_011521403.1:n.107+1_107+2delinsTA
XM_011523102.1:c.107+1_107+2delinsTA XP_011521404.1:n.107+1_107+2delinsTA
XM_011523103.1:c.107+1_107+2delinsTA XP_011521405.1:n.107+1_107+2delinsTA
XM_011523104.1:c.107+1_107+2delinsTA XP_011521406.1:n.107+1_107+2delinsTA
XM_011523105.1:c.107+1_107+2delinsTA XP_011521407.1:n.107+1_107+2delinsTA
XM_011523101.3:c.107+1_107+2delinsTA XP_011521403.1:n.107+1_107+2delinsTA
XM_011523103.3:c.107+1_107+2delinsTA XP_011521405.1:n.107+1_107+2delinsTA
XM_011523104.3:c.107+1_107+2delinsTA XP_011521406.1:n.107+1_107+2delinsTA
XM_011523105.3:c.107+1_107+2delinsTA XP_011521407.1:n.107+1_107+2delinsTA
XM_017023278.2:c.107+1_107+2delinsTA XP_016878767.1:n.107+1_107+2delinsTA
NM_016373.4:c.107+1_107+2delinsTA MANE Select NP_057457.1:n.107+1_107+2delinsTA
NM_001291997.2:c.-168+1_-168+2delinsTA NP_001278926.1:n.-168+1_-168+2delinsTA
NM_130791.4:c.107+1_107+2delinsTA NP_570607.1:n.107+1_107+2delinsTA
NR_120435.2:n.233_234delinsTA
NR_120436.2:n.233_234delinsTA
NM_130791.5:c.107+1_107+2delinsTA NP_570607.1:n.107+1_107+2delinsTA
NR_120436.3:n.233_234delinsTA