Canonical Allele Identifier: CA396842111
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 429263
ClinVar RCV Id: RCV000493734
dbSNP Id: rs1131691285

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78108487G>A , CM000678.2:g.78108487G>A GRCh38
NC_000016.9:g.78142384G>A , CM000678.1:g.78142384G>A GRCh37
NC_000016.8:g.76699885G>A NCBI36
NG_011698.1:g.13834G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.172G>A ENSP00000485925.2:p.Asp58Asn
ENST00000682609.1:n.499G>A
ENST00000683286.1:n.499G>A
ENST00000683929.1:c.172G>A ENSP00000507689.1:p.Asp58Asn
ENST00000684070.1:n.437-1291G>A
ENST00000684381.1:n.499G>A
ENST00000684452.1:n.499G>A
ENST00000684632.1:n.551G>A
ENST00000566780.6:c.172G>A MANE Select ENSP00000457230.1:p.Asp58Asn
ENST00000355860.7:c.172G>A ENSP00000348119.3:p.Asp58Asn
ENST00000402655.6:c.172G>A ENSP00000384238.2:p.Asp58Asn
ENST00000406884.6:c.172G>A ENSP00000384495.2:p.Asp58Asn
ENST00000408984.7:c.172G>A ENSP00000386161.3:p.Asp58Asn
ENST00000539474.6:c.172G>A ENSP00000445210.2:p.Asp58Asn
ENST00000561846.5:n.216G>A
ENST00000562214.5:n.295G>A
ENST00000563358.5:n.279G>A
ENST00000565562.5:n.217G>A
ENST00000566662.5:c.108-1291G>A ENSP00000454331.1:n.108-1291G>A
ENST00000566780.5:c.172G>A ENSP00000457230.1:p.Asp58Asn
ENST00000569332.5:c.108-1291G>A ENSP00000454788.1:n.108-1291G>A
ENST00000627394.2:c.108-1291G>A ENSP00000485925.1:n.108-1291G>A
NM_001291997.1:c.-167-1291G>A NP_001278926.1:n.-167-1291G>A
NM_016373.3:c.172G>A NP_057457.1:p.Asp58Asn
NM_130791.3:c.172G>A NP_570607.1:p.Asp58Asn
NR_120436.1:n.652G>A
XM_006721195.2:c.172G>A XP_006721258.1:p.Asp58Asn
XM_011523100.1:c.172G>A XP_011521402.1:p.Asp58Asn
XM_011523101.1:c.172G>A XP_011521403.1:p.Asp58Asn
XM_011523102.1:c.172G>A XP_011521404.1:p.Asp58Asn
XM_011523103.1:c.172G>A XP_011521405.1:p.Asp58Asn
XM_011523104.1:c.172G>A XP_011521406.1:p.Asp58Asn
XM_011523105.1:c.172G>A XP_011521407.1:p.Asp58Asn
XM_011523101.3:c.172G>A XP_011521403.1:p.Asp58Asn
XM_011523103.3:c.172G>A XP_011521405.1:p.Asp58Asn
XM_011523104.3:c.172G>A XP_011521406.1:p.Asp58Asn
XM_011523105.3:c.172G>A XP_011521407.1:p.Asp58Asn
XM_017023278.2:c.172G>A XP_016878767.1:p.Asp58Asn
NM_016373.4:c.172G>A MANE Select NP_057457.1:p.Asp58Asn
NM_001291997.2:c.-167-1291G>A NP_001278926.1:n.-167-1291G>A
NM_130791.4:c.172G>A NP_570607.1:p.Asp58Asn
NR_120436.2:n.411G>A
NM_130791.5:c.172G>A NP_570607.1:p.Asp58Asn
NR_120436.3:n.411G>A