Canonical Allele Identifier: CA2634409927
Gene: WWOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099678G>T , CM000678.2:g.78099678G>T GRCh38
NC_000016.9:g.78133575G>T , CM000678.1:g.78133575G>T GRCh37
NC_000016.8:g.76691076G>T NCBI36
NG_011698.1:g.5025G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-101G>T ENSP00000485925.2:n.-101G>T
ENST00000682609.1:n.227G>T
ENST00000683286.1:n.227G>T
ENST00000683929.1:c.-101G>T ENSP00000507689.1:n.-101G>T
ENST00000684070.1:n.229G>T
ENST00000684381.1:n.227G>T
ENST00000684452.1:n.227G>T
ENST00000684632.1:n.279G>T
ENST00000566780.6:c.-101G>T MANE Select ENSP00000457230.1:n.-101G>T
ENST00000402655.6:c.-101G>T ENSP00000384238.2:n.-101G>T
ENST00000406884.6:c.-101G>T ENSP00000384495.2:n.-101G>T
ENST00000539474.6:c.-101G>T ENSP00000445210.2:n.-101G>T
ENST00000562214.5:n.23G>T
ENST00000566662.5:c.-101G>T ENSP00000454331.1:n.-101G>T
ENST00000566780.5:c.-101G>T ENSP00000457230.1:n.-101G>T
ENST00000569332.5:c.-101G>T ENSP00000454788.1:n.-101G>T
ENST00000569818.1:c.-101G>T ENSP00000454485.1:n.-101G>T
ENST00000627394.2:c.-101G>T ENSP00000485925.1:n.-101G>T
NM_001291997.1:c.-375G>T NP_001278926.1:n.-375G>T
NM_016373.3:c.-101G>T NP_057457.1:n.-101G>T
NM_130791.3:c.-101G>T NP_570607.1:n.-101G>T
NR_120435.1:n.266G>T
NR_120436.1:n.266G>T
XM_006721195.2:c.-101G>T XP_006721258.1:n.-101G>T
XM_011523100.1:c.-101G>T XP_011521402.1:n.-101G>T
XM_011523101.1:c.-101G>T XP_011521403.1:n.-101G>T
XM_011523102.1:c.-101G>T XP_011521404.1:n.-101G>T
XM_011523103.1:c.-101G>T XP_011521405.1:n.-101G>T
XM_011523104.1:c.-101G>T XP_011521406.1:n.-101G>T
XM_011523105.1:c.-101G>T XP_011521407.1:n.-101G>T
XM_011523101.3:c.-101G>T XP_011521403.1:n.-101G>T
XM_011523103.3:c.-101G>T XP_011521405.1:n.-101G>T
XM_011523104.3:c.-101G>T XP_011521406.1:n.-101G>T
XM_011523105.3:c.-101G>T XP_011521407.1:n.-101G>T
XM_017023278.2:c.-101G>T XP_016878767.1:n.-101G>T
NM_016373.4:c.-101G>T MANE Select NP_057457.1:n.-101G>T
NM_001291997.2:c.-375G>T NP_001278926.1:n.-375G>T
NM_130791.4:c.-101G>T NP_570607.1:n.-101G>T
NR_120435.2:n.25G>T
NR_120436.2:n.25G>T
NM_130791.5:c.-101G>T NP_570607.1:n.-101G>T
NR_120436.3:n.25G>T