Canonical Allele Identifier: CA8182985

Gene: WWOX

Linked Data

• ClinVar Variation Id: 1039606
• ClinVar RCV Id: RCV001343112
• dbSNP Id: rs763124571
• ExAC: 16:78133750 AACC / A
• gnomAD v2: 16-78133750-AACC-A
• gnomAD v3: 16-78099853-AACC-A
• gnomAD v4: 16-78099853-AACC-A
• MyVariant Identifiers: chr16:g.78133751_78133753del (hg19) ; chr16:g.78099854_78099856del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099858_78099860del , CM000678.2:g.78099858_78099860del	GRCh38
NC_000016.9:g.78133755_78133757del , CM000678.1:g.78133755_78133757del	GRCh37
NC_000016.8:g.76691256_76691258del	NCBI36
NG_011698.1:g.5205_5207del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.80_82del	ENSP00000485925.2:p.Thr27del
ENST00000682609.1:n.407_409del
ENST00000683286.1:n.407_409del
ENST00000683929.1:c.80_82del	ENSP00000507689.1:p.Thr27del
ENST00000684070.1:n.409_411del
ENST00000684381.1:n.407_409del
ENST00000684452.1:n.407_409del
ENST00000684632.1:n.459_461del
ENST00000566780.6:c.80_82del MANE Select	ENSP00000457230.1:p.Thr27del
ENST00000355860.7:c.80_82del	ENSP00000348119.3:p.Thr27del
ENST00000402655.6:c.80_82del	ENSP00000384238.2:p.Thr27del
ENST00000406884.6:c.80_82del	ENSP00000384495.2:p.Thr27del
ENST00000408984.7:c.80_82del	ENSP00000386161.3:p.Thr27del
ENST00000539474.6:c.80_82del	ENSP00000445210.2:p.Thr27del
ENST00000561846.5:n.124_126del
ENST00000562214.5:n.203_205del
ENST00000563358.5:n.73_75del
ENST00000565562.5:n.125_127del
ENST00000566662.5:c.80_82del	ENSP00000454331.1:p.Thr27del
ENST00000566780.5:c.80_82del	ENSP00000457230.1:p.Thr27del
ENST00000569332.5:c.80_82del	ENSP00000454788.1:p.Thr27del
ENST00000569818.1:c.80_82del	ENSP00000454485.1:p.Thr27del
ENST00000627394.2:c.80_82del	ENSP00000485925.1:p.Thr27del
NM_001291997.1:c.-195_-193del	NP_001278926.1:n.-195_-193del
NM_016373.3:c.80_82del	NP_057457.1:p.Thr27del
NM_130791.3:c.80_82del	NP_570607.1:p.Thr27del
NR_120435.1:n.446_448del
NR_120436.1:n.446_448del
XM_006721195.2:c.80_82del	XP_006721258.1:p.Thr27del
XM_011523100.1:c.80_82del	XP_011521402.1:p.Thr27del
XM_011523101.1:c.80_82del	XP_011521403.1:p.Thr27del
XM_011523102.1:c.80_82del	XP_011521404.1:p.Thr27del
XM_011523103.1:c.80_82del	XP_011521405.1:p.Thr27del
XM_011523104.1:c.80_82del	XP_011521406.1:p.Thr27del
XM_011523105.1:c.80_82del	XP_011521407.1:p.Thr27del
XM_011523101.3:c.80_82del	XP_011521403.1:p.Thr27del
XM_011523103.3:c.80_82del	XP_011521405.1:p.Thr27del
XM_011523104.3:c.80_82del	XP_011521406.1:p.Thr27del
XM_011523105.3:c.80_82del	XP_011521407.1:p.Thr27del
XM_017023278.2:c.80_82del	XP_016878767.1:p.Thr27del
NM_016373.4:c.80_82del MANE Select	NP_057457.1:p.Thr27del
NM_001291997.2:c.-195_-193del	NP_001278926.1:n.-195_-193del
NM_130791.4:c.80_82del	NP_570607.1:p.Thr27del
NR_120435.2:n.205_207del
NR_120436.2:n.205_207del
NM_130791.5:c.80_82del	NP_570607.1:p.Thr27del
NR_120436.3:n.205_207del