Canonical Allele Identifier: CA2234946536
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78224932C= , CM000678.2:g.78224932C= GRCh38
NC_000016.9:g.78258829C= , CM000678.1:g.78258829C= GRCh37
NC_000016.8:g.76816330C= NCBI36
NG_011698.1:g.130279C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.516+60643C= ENSP00000485925.2:n.516+60643C=
ENST00000683286.1:n.843+60643C=
ENST00000683929.1:c.516+60643C= ENSP00000507689.1:n.516+60643C=
ENST00000684070.1:n.780+60643C=
ENST00000684632.1:n.895+60643C=
ENST00000566780.6:c.516+60643C= MANE Select ENSP00000457230.1:n.516+60643C=
ENST00000355860.7:c.517-53671C= ENSP00000348119.3:n.517-53671C=
ENST00000402655.6:c.409+109778C= ENSP00000384238.2:n.409+109778C=
ENST00000406884.6:c.516+60643C= ENSP00000384495.2:n.516+60643C=
ENST00000408984.7:c.516+60643C= ENSP00000386161.3:n.516+60643C=
ENST00000539474.6:c.409+109778C= ENSP00000445210.2:n.409+109778C=
ENST00000561846.5:n.561-55909C=
ENST00000562639.5:n.204+60643C=
ENST00000563358.5:n.624-53671C=
ENST00000565791.1:n.204-39537C=
ENST00000566662.5:c.*134+60643C= ENSP00000454331.1:n.*134+60643C=
ENST00000566780.5:c.516+60643C= ENSP00000457230.1:n.516+60643C=
ENST00000569332.5:c.*313+60643C= ENSP00000454788.1:n.*313+60643C=
ENST00000627394.2:c.*314-53671C= ENSP00000485925.1:n.*314-53671C=
NM_001291997.1:c.177+60643C= NP_001278926.1:n.177+60643C=
NM_016373.3:c.516+60643C= NP_057457.1:n.516+60643C=
NM_130791.3:c.517-53671C= NP_570607.1:n.517-53671C=
NR_120436.1:n.997-53671C=
XM_006721195.2:c.516+60643C= XP_006721258.1:n.516+60643C=
XM_011523100.1:c.516+60643C= XP_011521402.1:n.516+60643C=
XM_011523101.1:c.516+60643C= XP_011521403.1:n.516+60643C=
XM_011523102.1:c.516+60643C= XP_011521404.1:n.516+60643C=
XM_011523103.1:c.516+60643C= XP_011521405.1:n.516+60643C=
XM_011523104.1:c.516+60643C= XP_011521406.1:n.516+60643C=
XM_011523105.1:c.517-3848C= XP_011521407.1:n.517-3848C=
XM_011523101.3:c.516+60643C= XP_011521403.1:n.516+60643C=
XM_011523103.3:c.516+60643C= XP_011521405.1:n.516+60643C=
XM_011523104.3:c.516+60643C= XP_011521406.1:n.516+60643C=
XM_011523105.3:c.517-3848C= XP_011521407.1:n.517-3848C=
XM_017023278.2:c.516+60643C= XP_016878767.1:n.516+60643C=
NM_016373.4:c.516+60643C= MANE Select NP_057457.1:n.516+60643C=
NM_001291997.2:c.177+60643C= NP_001278926.1:n.177+60643C=
NM_130791.4:c.517-53671C= NP_570607.1:n.517-53671C=
NR_120436.2:n.756-53671C=
NM_130791.5:c.517-53671C= NP_570607.1:n.517-53671C=
NR_120436.3:n.756-53671C=