Canonical Allele Identifier: CA2234888520
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099480_78099482delinsATC , CM000678.2:g.78099480_78099482delinsATC GRCh38
NC_000016.9:g.78133377_78133379delinsATC , CM000678.1:g.78133377_78133379delinsATC GRCh37
NC_000016.8:g.76690878_76690880delinsATC NCBI36
NG_011698.1:g.4827_4829delinsATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-299_-297delinsATC ENSP00000485925.2:n.-299_-297delinsATC
ENST00000682609.1:n.29_31delinsATC
ENST00000683286.1:n.29_31delinsATC
ENST00000683929.1:c.-299_-297delinsATC ENSP00000507689.1:n.-299_-297delinsATC
ENST00000684070.1:n.31_33delinsATC
ENST00000684381.1:n.29_31delinsATC
ENST00000684452.1:n.29_31delinsATC
ENST00000684632.1:n.81_83delinsATC
ENST00000566780.5:c.-299_-297delinsATC ENSP00000457230.1:n.-299_-297delinsATC
ENST00000627394.2:c.-299_-297delinsATC ENSP00000485925.1:n.-299_-297delinsATC
NM_001291997.1:c.-573_-571delinsATC NP_001278926.1:n.-573_-571delinsATC
NM_016373.3:c.-299_-297delinsATC NP_057457.1:n.-299_-297delinsATC
NM_130791.3:c.-299_-297delinsATC NP_570607.1:n.-299_-297delinsATC
NR_120435.1:n.68_70delinsATC
NR_120436.1:n.68_70delinsATC