Canonical Allele Identifier: CA14329812
Gene: WWOX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78301147A>G , CM000678.2:g.78301147A>G GRCh38
NC_000016.9:g.78335044A>G , CM000678.1:g.78335044A>G GRCh37
NC_000016.8:g.76892545A>G NCBI36
NG_011698.1:g.206494A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.517-85713A>G ENSP00000485925.2:n.517-85713A>G
ENST00000683286.1:n.844-2191A>G
ENST00000683929.1:c.517-85713A>G ENSP00000507689.1:n.517-85713A>G
ENST00000684070.1:n.781-85713A>G
ENST00000684632.1:n.896-85713A>G
ENST00000566780.6:c.517-85713A>G MANE Select ENSP00000457230.1:n.517-85713A>G
ENST00000402655.6:c.409+185993A>G ENSP00000384238.2:n.409+185993A>G
ENST00000406884.6:c.516+136858A>G ENSP00000384495.2:n.516+136858A>G
ENST00000408984.7:c.517-85713A>G ENSP00000386161.3:n.517-85713A>G
ENST00000539474.6:c.409+185993A>G ENSP00000445210.2:n.409+185993A>G
ENST00000562639.5:n.205-85713A>G
ENST00000566662.5:c.*135-85713A>G ENSP00000454331.1:n.*135-85713A>G
ENST00000566780.5:c.517-85713A>G ENSP00000457230.1:n.517-85713A>G
ENST00000569332.5:c.*314-85713A>G ENSP00000454788.1:n.*314-85713A>G
NM_001291997.1:c.178-85713A>G NP_001278926.1:n.178-85713A>G
NM_016373.3:c.517-85713A>G NP_057457.1:n.517-85713A>G
XM_006721195.2:c.517-85713A>G XP_006721258.1:n.517-85713A>G
XM_011523100.1:c.517-85713A>G XP_011521402.1:n.517-85713A>G
XM_011523101.1:c.517-85713A>G XP_011521403.1:n.517-85713A>G
XM_011523102.1:c.517-85713A>G XP_011521404.1:n.517-85713A>G
XM_011523103.1:c.517-85713A>G XP_011521405.1:n.517-85713A>G
XM_011523104.1:c.517-85713A>G XP_011521406.1:n.517-85713A>G
XM_011523101.3:c.517-85713A>G XP_011521403.1:n.517-85713A>G
XM_011523103.3:c.517-85713A>G XP_011521405.1:n.517-85713A>G
XM_011523104.3:c.517-85713A>G XP_011521406.1:n.517-85713A>G
XM_017023278.2:c.517-50836A>G XP_016878767.1:n.517-50836A>G
NM_016373.4:c.517-85713A>G MANE Select NP_057457.1:n.517-85713A>G
NM_001291997.2:c.178-85713A>G NP_001278926.1:n.178-85713A>G
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