Canonical Allele Identifier: CA658683971
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 493191
dbSNP Id: rs1555532979

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099887_78099890del , CM000678.2:g.78099887_78099890del GRCh38
NC_000016.9:g.78133784_78133787del , CM000678.1:g.78133784_78133787del GRCh37
NC_000016.8:g.76691285_76691288del NCBI36
NG_011698.1:g.5234_5237del

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.107+2_107+5del
ENST00000682609.1:n.434+2_434+5del
ENST00000683286.1:n.434+2_434+5del
ENST00000683929.1:c.107+2_107+5del
ENST00000684070.1:n.436+2_436+5del
ENST00000684381.1:n.434+2_434+5del
ENST00000684452.1:n.434+2_434+5del
ENST00000684632.1:n.486+2_486+5del
ENST00000566780.6:c.107+2_107+5del
ENST00000355860.7:c.107+2_107+5del
ENST00000402655.6:c.107+2_107+5del
ENST00000406884.6:c.107+2_107+5del
ENST00000408984.7:c.107+2_107+5del
ENST00000539474.6:c.107+2_107+5del
ENST00000561846.5:n.151+2_151+5del
ENST00000562214.5:n.230+2_230+5del
ENST00000563358.5:n.102_105del
ENST00000565562.5:n.152+2_152+5del
ENST00000566662.5:c.107+2_107+5del
ENST00000566780.5:c.107+2_107+5del
ENST00000569332.5:c.107+2_107+5del
ENST00000569818.1:c.109_*1del ENSP00000454485.1:n.[c.109_*1del;Ter37GlyextTer?]
ENST00000627394.2:c.107+2_107+5del
NM_001291997.1:c.-168+2_-168+5del
NM_016373.3:c.107+2_107+5del
NM_130791.3:c.107+2_107+5del
NR_120435.1:n.475_478del
NR_120436.1:n.475_478del
XM_006721195.2:c.107+2_107+5del
XM_011523100.1:c.107+2_107+5del
XM_011523101.1:c.107+2_107+5del
XM_011523102.1:c.107+2_107+5del
XM_011523103.1:c.107+2_107+5del
XM_011523104.1:c.107+2_107+5del
XM_011523105.1:c.107+2_107+5del
XM_011523101.3:c.107+2_107+5del
XM_011523103.3:c.107+2_107+5del
XM_011523104.3:c.107+2_107+5del
XM_011523105.3:c.107+2_107+5del
XM_017023278.2:c.107+2_107+5del
NM_016373.4:c.107+2_107+5del
NM_001291997.2:c.-168+2_-168+5del
NM_130791.4:c.107+2_107+5del
NR_120435.2:n.234_237del
NR_120436.2:n.234_237del
NM_130791.5:c.107+2_107+5del
NR_120436.3:n.234_237del