Canonical Allele Identifier: CA117326
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 5203
dbSNP Id: rs119487098

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78432568T>C , CM000678.2:g.78432568T>C GRCh38
NC_000016.9:g.78466465T>C , CM000678.1:g.78466465T>C GRCh37
NC_000016.8:g.77023966T>C NCBI36
NG_011698.1:g.337915T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000627394.3:c.872T>C ENSP00000485925.2:p.Leu291Pro
ENST00000683929.1:c.872T>C ENSP00000507689.1:p.Leu291Pro
ENST00000684632.1:n.1251T>C
ENST00000566780.6:c.872T>C MANE Select ENSP00000457230.1:p.Leu291Pro
ENST00000402655.6:c.409+317414T>C ENSP00000384238.2:n.409+317414T>C
ENST00000406884.6:c.516+268279T>C ENSP00000384495.2:n.516+268279T>C
ENST00000408984.7:c.872T>C ENSP00000386161.3:p.Leu291Pro
ENST00000539474.6:c.409+317414T>C ENSP00000445210.2:n.409+317414T>C
ENST00000562639.5:n.560T>C
ENST00000566780.5:c.872T>C ENSP00000457230.1:p.Leu291Pro
ENST00000569332.5:c.*669T>C ENSP00000454788.1:n.*669T>C
ENST00000620008.1:c.266T>C ENSP00000482648.1:p.Leu89Pro
NM_001291997.1:c.533T>C NP_001278926.1:p.Leu178Pro
NM_016373.3:c.872T>C NP_057457.1:p.Leu291Pro
XM_006721195.2:c.872T>C XP_006721258.1:p.Leu291Pro
XM_011523100.1:c.872T>C XP_011521402.1:p.Leu291Pro
XM_011523101.1:c.872T>C XP_011521403.1:p.Leu291Pro
XM_011523102.1:c.872T>C XP_011521404.1:p.Leu291Pro
XM_011523103.1:c.872T>C XP_011521405.1:p.Leu291Pro
XM_011523104.1:c.872T>C XP_011521406.1:p.Leu291Pro
XR_933765.1:n.3418+1752A>G
XM_011523101.3:c.872T>C XP_011521403.1:p.Leu291Pro
XM_011523103.3:c.872T>C XP_011521405.1:p.Leu291Pro
XM_011523104.3:c.872T>C XP_011521406.1:p.Leu291Pro
NM_016373.4:c.872T>C MANE Select NP_057457.1:p.Leu291Pro
NM_001291997.2:c.533T>C NP_001278926.1:p.Leu178Pro