Canonical Allele Identifier: CA8183386
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 260743
dbSNP Id: rs74860463

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78424877C>A , CM000678.2:g.78424877C>A GRCh38
NC_000016.9:g.78458774C>A , CM000678.1:g.78458774C>A GRCh37
NC_000016.8:g.77016275C>A NCBI36
NG_011698.1:g.330224C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000627394.3:c.613C>A ENSP00000485925.2:p.His205Asn
ENST00000683929.1:c.613C>A ENSP00000507689.1:p.His205Asn
ENST00000684632.1:n.992C>A
ENST00000566780.6:c.613C>A MANE Select ENSP00000457230.1:p.His205Asn
ENST00000402655.6:c.409+309723C>A ENSP00000384238.2:n.409+309723C>A
ENST00000406884.6:c.516+260588C>A ENSP00000384495.2:n.516+260588C>A
ENST00000408984.7:c.613C>A ENSP00000386161.3:p.His205Asn
ENST00000539474.6:c.409+309723C>A ENSP00000445210.2:n.409+309723C>A
ENST00000562639.5:n.301C>A
ENST00000566662.5:c.*231C>A ENSP00000454331.1:n.*231C>A
ENST00000566780.5:c.613C>A ENSP00000457230.1:p.His205Asn
ENST00000569332.5:c.*410C>A ENSP00000454788.1:n.*410C>A
ENST00000620008.1:c.7C>A ENSP00000482648.1:p.His3Asn
NM_001291997.1:c.274C>A NP_001278926.1:p.His92Asn
NM_016373.3:c.613C>A NP_057457.1:p.His205Asn
XM_006721195.2:c.613C>A XP_006721258.1:p.His205Asn
XM_011523100.1:c.613C>A XP_011521402.1:p.His205Asn
XM_011523101.1:c.613C>A XP_011521403.1:p.His205Asn
XM_011523102.1:c.613C>A XP_011521404.1:p.His205Asn
XM_011523103.1:c.613C>A XP_011521405.1:p.His205Asn
XM_011523104.1:c.613C>A XP_011521406.1:p.His205Asn
XR_933765.1:n.3806+5549G>T
XM_011523101.3:c.613C>A XP_011521403.1:p.His205Asn
XM_011523103.3:c.613C>A XP_011521405.1:p.His205Asn
XM_011523104.3:c.613C>A XP_011521406.1:p.His205Asn
NM_016373.4:c.613C>A MANE Select NP_057457.1:p.His205Asn
NM_001291997.2:c.274C>A NP_001278926.1:p.His92Asn