Canonical Allele Identifier: CA2634409840
Gene: WWOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099612_78099619del , CM000678.2:g.78099612_78099619del GRCh38
NC_000016.9:g.78133509_78133516del , CM000678.1:g.78133509_78133516del GRCh37
NC_000016.8:g.76691010_76691017del NCBI36
NG_011698.1:g.4959_4966del

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-167_-160del ENSP00000485925.2:n.-167_-160del
ENST00000682609.1:n.161_168del
ENST00000683286.1:n.161_168del
ENST00000683929.1:c.-167_-160del ENSP00000507689.1:n.-167_-160del
ENST00000684070.1:n.163_170del
ENST00000684381.1:n.161_168del
ENST00000684452.1:n.161_168del
ENST00000684632.1:n.213_220del
ENST00000566780.5:c.-167_-160del ENSP00000457230.1:n.-167_-160del
ENST00000627394.2:c.-167_-160del ENSP00000485925.1:n.-167_-160del
NM_001291997.1:c.-441_-434del NP_001278926.1:n.-441_-434del
NM_016373.3:c.-167_-160del NP_057457.1:n.-167_-160del
NM_130791.3:c.-167_-160del NP_570607.1:n.-167_-160del
NR_120435.1:n.200_207del
NR_120436.1:n.200_207del