Canonical Allele Identifier: CA8183409
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 387873
dbSNP Id: rs72549408

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78424933T>C , CM000678.2:g.78424933T>C GRCh38
NC_000016.9:g.78458830T>C , CM000678.1:g.78458830T>C GRCh37
NC_000016.8:g.77016331T>C NCBI36
NG_011698.1:g.330280T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.669T>C ENSP00000485925.2:p.Asp223=
ENST00000683929.1:c.669T>C ENSP00000507689.1:p.Asp223=
ENST00000684632.1:n.1048T>C
ENST00000566780.6:c.669T>C MANE Select ENSP00000457230.1:p.Asp223=
ENST00000402655.6:c.409+309779T>C ENSP00000384238.2:n.409+309779T>C
ENST00000406884.6:c.516+260644T>C ENSP00000384495.2:n.516+260644T>C
ENST00000408984.7:c.669T>C ENSP00000386161.3:p.Asp223=
ENST00000539474.6:c.409+309779T>C ENSP00000445210.2:n.409+309779T>C
ENST00000562639.5:n.357T>C
ENST00000566662.5:c.*287T>C ENSP00000454331.1:n.*287T>C
ENST00000566780.5:c.669T>C ENSP00000457230.1:p.Asp223=
ENST00000569332.5:c.*466T>C ENSP00000454788.1:n.*466T>C
ENST00000620008.1:c.63T>C ENSP00000482648.1:p.Asp21=
NM_001291997.1:c.330T>C NP_001278926.1:p.Asp110=
NM_016373.3:c.669T>C NP_057457.1:p.Asp223=
XM_006721195.2:c.669T>C XP_006721258.1:p.Asp223=
XM_011523100.1:c.669T>C XP_011521402.1:p.Asp223=
XM_011523101.1:c.669T>C XP_011521403.1:p.Asp223=
XM_011523102.1:c.669T>C XP_011521404.1:p.Asp223=
XM_011523103.1:c.669T>C XP_011521405.1:p.Asp223=
XM_011523104.1:c.669T>C XP_011521406.1:p.Asp223=
XR_933765.1:n.3806+5493A>G
XM_011523101.3:c.669T>C XP_011521403.1:p.Asp223=
XM_011523103.3:c.669T>C XP_011521405.1:p.Asp223=
XM_011523104.3:c.669T>C XP_011521406.1:p.Asp223=
NM_016373.4:c.669T>C MANE Select NP_057457.1:p.Asp223=
NM_001291997.2:c.330T>C NP_001278926.1:p.Asp110=