Canonical Allele Identifier: CA2634409678
Gene: WWOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099463_78099464insCCAGCGCAGCGCGTGCG , CM000678.2:g.78099463_78099464insCCAGCGCAGCGCGTGCG GRCh38
NC_000016.9:g.78133360_78133361insCCAGCGCAGCGCGTGCG , CM000678.1:g.78133360_78133361insCCAGCGCAGCGCGTGCG GRCh37
NC_000016.8:g.76690861_76690862insCCAGCGCAGCGCGTGCG NCBI36
NG_011698.1:g.4810_4811insCCAGCGCAGCGCGTGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-316_-315insCCAGCGCAGCGCGTGCG ENSP00000485925.2:n.-316_-315insCCAGCGCAGCGCGTGCG
ENST00000682609.1:n.12_13insCCAGCGCAGCGCGTGCG
ENST00000683286.1:n.12_13insCCAGCGCAGCGCGTGCG
ENST00000683929.1:c.-316_-315insCCAGCGCAGCGCGTGCG ENSP00000507689.1:n.-316_-315insCCAGCGCAGCGCGTGCG
ENST00000684070.1:n.14_15insCCAGCGCAGCGCGTGCG
ENST00000684381.1:n.12_13insCCAGCGCAGCGCGTGCG
ENST00000684452.1:n.12_13insCCAGCGCAGCGCGTGCG
ENST00000684632.1:n.64_65insCCAGCGCAGCGCGTGCG
ENST00000566780.5:c.-316_-315insCCAGCGCAGCGCGTGCG ENSP00000457230.1:n.-316_-315insCCAGCGCAGCGCGTGCG
ENST00000627394.2:c.-316_-315insCCAGCGCAGCGCGTGCG ENSP00000485925.1:n.-316_-315insCCAGCGCAGCGCGTGCG
NM_001291997.1:c.-590_-589insCCAGCGCAGCGCGTGCG NP_001278926.1:n.-590_-589insCCAGCGCAGCGCGTGCG
NM_016373.3:c.-316_-315insCCAGCGCAGCGCGTGCG NP_057457.1:n.-316_-315insCCAGCGCAGCGCGTGCG
NM_130791.3:c.-316_-315insCCAGCGCAGCGCGTGCG NP_570607.1:n.-316_-315insCCAGCGCAGCGCGTGCG
NR_120435.1:n.51_52insCCAGCGCAGCGCGTGCG
NR_120436.1:n.51_52insCCAGCGCAGCGCGTGCG