Canonical Allele Identifier: CA8183207
Gene: WWOX HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78164180T>C , CM000678.2:g.78164180T>C GRCh38
NC_000016.9:g.78198077T>C , CM000678.1:g.78198077T>C GRCh37
NC_000016.8:g.76755578T>C NCBI36
NG_011698.1:g.69527T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.410-3T>C ENSP00000485925.2:n.410-3T>C
ENST00000683286.1:n.737-3T>C
ENST00000683929.1:c.410-3T>C ENSP00000507689.1:n.410-3T>C
ENST00000684070.1:n.674-3T>C
ENST00000684632.1:n.789-3T>C
ENST00000566780.6:c.410-3T>C MANE Select ENSP00000457230.1:n.410-3T>C
ENST00000355860.7:c.410-3T>C ENSP00000348119.3:n.410-3T>C
ENST00000402655.6:c.409+49026T>C ENSP00000384238.2:n.409+49026T>C
ENST00000406884.6:c.410-3T>C ENSP00000384495.2:n.410-3T>C
ENST00000408984.7:c.410-3T>C ENSP00000386161.3:n.410-3T>C
ENST00000539474.6:c.409+49026T>C ENSP00000445210.2:n.409+49026T>C
ENST00000561846.5:n.454-3T>C
ENST00000562639.5:n.98-3T>C
ENST00000563358.5:n.517-3T>C
ENST00000565791.1:n.18-3T>C
ENST00000566662.5:c.*28-3T>C ENSP00000454331.1:n.*28-3T>C
ENST00000566780.5:c.410-3T>C ENSP00000457230.1:n.410-3T>C
ENST00000569332.5:c.*207-3T>C ENSP00000454788.1:n.*207-3T>C
ENST00000627394.2:c.*207-3T>C ENSP00000485925.1:n.*207-3T>C
NM_001291997.1:c.71-3T>C NP_001278926.1:n.71-3T>C
NM_016373.3:c.410-3T>C NP_057457.1:n.410-3T>C
NM_130791.3:c.410-3T>C NP_570607.1:n.410-3T>C
NR_120436.1:n.890-3T>C
XM_006721195.2:c.410-3T>C XP_006721258.1:n.410-3T>C
XM_011523100.1:c.410-3T>C XP_011521402.1:n.410-3T>C
XM_011523101.1:c.410-3T>C XP_011521403.1:n.410-3T>C
XM_011523102.1:c.410-3T>C XP_011521404.1:n.410-3T>C
XM_011523103.1:c.410-3T>C XP_011521405.1:n.410-3T>C
XM_011523104.1:c.410-3T>C XP_011521406.1:n.410-3T>C
XM_011523105.1:c.410-3T>C XP_011521407.1:n.410-3T>C
XM_011523101.3:c.410-3T>C XP_011521403.1:n.410-3T>C
XM_011523103.3:c.410-3T>C XP_011521405.1:n.410-3T>C
XM_011523104.3:c.410-3T>C XP_011521406.1:n.410-3T>C
XM_011523105.3:c.410-3T>C XP_011521407.1:n.410-3T>C
XM_017023278.2:c.410-3T>C XP_016878767.1:n.410-3T>C
NM_016373.4:c.410-3T>C MANE Select NP_057457.1:n.410-3T>C
NM_001291997.2:c.71-3T>C NP_001278926.1:n.71-3T>C
NM_130791.4:c.410-3T>C NP_570607.1:n.410-3T>C
NR_120436.2:n.649-3T>C
NM_130791.5:c.410-3T>C NP_570607.1:n.410-3T>C
NR_120436.3:n.649-3T>C