Canonical Allele Identifier: CA2634409711
Gene: WWOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099499_78099500del , CM000678.2:g.78099499_78099500del GRCh38
NC_000016.9:g.78133396_78133397del , CM000678.1:g.78133396_78133397del GRCh37
NC_000016.8:g.76690897_76690898del NCBI36
NG_011698.1:g.4846_4847del

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-280_-279del ENSP00000485925.2:n.-280_-279del
ENST00000682609.1:n.48_49del
ENST00000683286.1:n.48_49del
ENST00000683929.1:c.-280_-279del ENSP00000507689.1:n.-280_-279del
ENST00000684070.1:n.50_51del
ENST00000684381.1:n.48_49del
ENST00000684452.1:n.48_49del
ENST00000684632.1:n.100_101del
ENST00000566780.5:c.-280_-279del ENSP00000457230.1:n.-280_-279del
ENST00000627394.2:c.-280_-279del ENSP00000485925.1:n.-280_-279del
NM_001291997.1:c.-554_-553del NP_001278926.1:n.-554_-553del
NM_016373.3:c.-280_-279del NP_057457.1:n.-280_-279del
NM_130791.3:c.-280_-279del NP_570607.1:n.-280_-279del
NR_120435.1:n.87_88del
NR_120436.1:n.87_88del