Canonical Allele Identifier: CA2234901776
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78108451_78108452delinsCA , CM000678.2:g.78108451_78108452delinsCA GRCh38
NC_000016.9:g.78142348_78142349delinsCA , CM000678.1:g.78142348_78142349delinsCA GRCh37
NC_000016.8:g.76699849_76699850delinsCA NCBI36
NG_011698.1:g.13798_13799delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000627394.3:c.136_137delinsCA ENSP00000485925.2:p.His46=
ENST00000682609.1:n.463_464delinsCA
ENST00000683286.1:n.463_464delinsCA
ENST00000683929.1:c.136_137delinsCA ENSP00000507689.1:p.His46=
ENST00000684070.1:n.437-1327_437-1326delinsCA
ENST00000684381.1:n.463_464delinsCA
ENST00000684452.1:n.463_464delinsCA
ENST00000684632.1:n.515_516delinsCA
ENST00000566780.6:c.136_137delinsCA MANE Select ENSP00000457230.1:p.His46=
ENST00000355860.7:c.136_137delinsCA ENSP00000348119.3:p.His46=
ENST00000402655.6:c.136_137delinsCA ENSP00000384238.2:p.His46=
ENST00000406884.6:c.136_137delinsCA ENSP00000384495.2:p.His46=
ENST00000408984.7:c.136_137delinsCA ENSP00000386161.3:p.His46=
ENST00000539474.6:c.136_137delinsCA ENSP00000445210.2:p.His46=
ENST00000561846.5:n.180_181delinsCA
ENST00000562214.5:n.259_260delinsCA
ENST00000563358.5:n.243_244delinsCA
ENST00000565562.5:n.181_182delinsCA
ENST00000566662.5:c.108-1327_108-1326delinsCA ENSP00000454331.1:n.108-1327_108-1326deli...
ENST00000566780.5:c.136_137delinsCA ENSP00000457230.1:p.His46=
ENST00000569332.5:c.108-1327_108-1326delinsCA ENSP00000454788.1:n.108-1327_108-1326deli...
ENST00000627394.2:c.108-1327_108-1326delinsCA ENSP00000485925.1:n.108-1327_108-1326deli...
NM_001291997.1:c.-167-1327_-167-1326delinsCA NP_001278926.1:n.-167-1327_-167-1326delin...
NM_016373.3:c.136_137delinsCA NP_057457.1:p.His46=
NM_130791.3:c.136_137delinsCA NP_570607.1:p.His46=
NR_120436.1:n.616_617delinsCA
XM_006721195.2:c.136_137delinsCA XP_006721258.1:p.His46=
XM_011523100.1:c.136_137delinsCA XP_011521402.1:p.His46=
XM_011523101.1:c.136_137delinsCA XP_011521403.1:p.His46=
XM_011523102.1:c.136_137delinsCA XP_011521404.1:p.His46=
XM_011523103.1:c.136_137delinsCA XP_011521405.1:p.His46=
XM_011523104.1:c.136_137delinsCA XP_011521406.1:p.His46=
XM_011523105.1:c.136_137delinsCA XP_011521407.1:p.His46=
XM_011523101.3:c.136_137delinsCA XP_011521403.1:p.His46=
XM_011523103.3:c.136_137delinsCA XP_011521405.1:p.His46=
XM_011523104.3:c.136_137delinsCA XP_011521406.1:p.His46=
XM_011523105.3:c.136_137delinsCA XP_011521407.1:p.His46=
XM_017023278.2:c.136_137delinsCA XP_016878767.1:p.His46=
NM_016373.4:c.136_137delinsCA MANE Select NP_057457.1:p.His46=
NM_001291997.2:c.-167-1327_-167-1326delinsCA NP_001278926.1:n.-167-1327_-167-1326delin...
NM_130791.4:c.136_137delinsCA NP_570607.1:p.His46=
NR_120436.2:n.375_376delinsCA
NM_130791.5:c.136_137delinsCA NP_570607.1:p.His46=
NR_120436.3:n.375_376delinsCA