Canonical Allele Identifier: CA14286930
Gene: WWOX HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1079572

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78153241G>A , CM000678.2:g.78153241G>A GRCh38
NC_000016.9:g.78187138G>A , CM000678.1:g.78187138G>A GRCh37
NC_000016.8:g.76744639G>A NCBI36
NG_011698.1:g.58588G>A

Transcript Alleles

HGVS Amino-acid change
NM_001291997.1:c.71-10942G>A VV NP_001278926.1:p.=
NM_016373.3:c.410-10942G>A VV NP_057457.1:p.=
NM_130791.3:c.410-10942G>A VV NP_570607.1:p.=
NR_120436.1:n.890-10942G>A
XM_006721195.2:c.410-10942G>A XP_006721258.1:p.=
XM_011523100.1:c.410-10942G>A XP_011521402.1:p.=
XM_011523101.1:c.410-10942G>A XP_011521403.1:p.=
XM_011523102.1:c.410-10942G>A XP_011521404.1:p.=
XM_011523103.1:c.410-10942G>A XP_011521405.1:p.=
XM_011523104.1:c.410-10942G>A XP_011521406.1:p.=
XM_011523105.1:c.410-10942G>A XP_011521407.1:p.=
XM_011523101.3:c.410-10942G>A
XM_011523103.3:c.410-10942G>A
XM_011523104.3:c.410-10942G>A
XM_011523105.3:c.410-10942G>A
XM_017023278.2:c.410-10942G>A XP_016878767.1:p.=
ENST00000355860.7:c.410-10942G>A ENSP00000348119.3:p.=
ENST00000402655.6:c.409+38087G>A ENSP00000384238.2:p.=
ENST00000406884.6:c.410-10942G>A ENSP00000384495.2:p.=
ENST00000408984.7:c.410-10942G>A ENSP00000386161.3:p.=
ENST00000539474.6:c.409+38087G>A ENSP00000445210.2:p.=
ENST00000561846.5:n.454-10942G>A
ENST00000562639.5:n.98-10942G>A
ENST00000563358.5:n.517-10942G>A
ENST00000565791.1:n.17+7308G>A
ENST00000566662.5:c.*28-10942G>A ENSP00000454331.1:p.=
ENST00000566780.5:c.410-10942G>A ENSP00000457230.1:p.=
ENST00000569332.5:c.*207-10942G>A ENSP00000454788.1:p.=
ENST00000627394.2:c.*207-10942G>A ENSP00000485925.1:p.=