Canonical Allele Identifier: CA2634410029
Gene: WWOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099857_78099968del , CM000678.2:g.78099857_78099968del GRCh38
NC_000016.9:g.78133754_78133865del , CM000678.1:g.78133754_78133865del GRCh37
NC_000016.8:g.76691255_76691366del NCBI36
NG_011698.1:g.5204_5315del

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.79_107+83del
ENST00000682609.1:n.406_434+83del
ENST00000683286.1:n.406_434+83del
ENST00000683929.1:c.79_107+83del
ENST00000684070.1:n.408_436+83del
ENST00000684381.1:n.406_434+83del
ENST00000684452.1:n.406_434+83del
ENST00000684632.1:n.458_486+83del
ENST00000566780.6:c.79_107+83del
ENST00000355860.7:c.79_107+83del
ENST00000402655.6:c.79_107+83del
ENST00000406884.6:c.79_107+83del
ENST00000408984.7:c.79_107+83del
ENST00000539474.6:c.79_107+83del
ENST00000561846.5:n.123_151+83del
ENST00000562214.5:n.202_230+83del
ENST00000563358.5:n.72_183del
ENST00000565562.5:n.124_152+83del
ENST00000566662.5:c.79_107+83del
ENST00000566780.5:c.79_107+83del
ENST00000569332.5:c.79_107+83del
ENST00000569818.1:c.79_*79del ENSP00000454485.1:n.[c.79_*79del;Thr27SerfsTer14]
ENST00000627394.2:c.79_107+83del
NM_001291997.1:c.-196_-168+83del
NM_016373.3:c.79_107+83del
NM_130791.3:c.79_107+83del
NR_120435.1:n.445_556del
NR_120436.1:n.445_556del
XM_006721195.2:c.79_107+83del
XM_011523100.1:c.79_107+83del
XM_011523101.1:c.79_107+83del
XM_011523102.1:c.79_107+83del
XM_011523103.1:c.79_107+83del
XM_011523104.1:c.79_107+83del
XM_011523105.1:c.79_107+83del
XM_011523101.3:c.79_107+83del
XM_011523103.3:c.79_107+83del
XM_011523104.3:c.79_107+83del
XM_011523105.3:c.79_107+83del
XM_017023278.2:c.79_107+83del
NM_016373.4:c.79_107+83del
NM_001291997.2:c.-196_-168+83del
NM_130791.4:c.79_107+83del
NR_120435.2:n.204_315del
NR_120436.2:n.204_315del
NM_130791.5:c.79_107+83del
NR_120436.3:n.204_315del