Canonical Allele Identifier: CA2234888963

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099710_78099714delinsGGAGT , CM000678.2:g.78099710_78099714delinsGGAGT	GRCh38
NC_000016.9:g.78133607_78133611delinsGGAGT , CM000678.1:g.78133607_78133611delinsGGAGT	GRCh37
NC_000016.8:g.76691108_76691112delinsGGAGT	NCBI36
NG_011698.1:g.5057_5061delinsGGAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-69_-65delinsGGAGT	ENSP00000485925.2:n.-69_-65delinsGGAGT
ENST00000682609.1:n.259_263delinsGGAGT
ENST00000683286.1:n.259_263delinsGGAGT
ENST00000683929.1:c.-69_-65delinsGGAGT	ENSP00000507689.1:n.-69_-65delinsGGAGT
ENST00000684070.1:n.261_265delinsGGAGT
ENST00000684381.1:n.259_263delinsGGAGT
ENST00000684452.1:n.259_263delinsGGAGT
ENST00000684632.1:n.311_315delinsGGAGT
ENST00000566780.6:c.-69_-65delinsGGAGT MANE Select	ENSP00000457230.1:n.-69_-65delinsGGAGT
ENST00000355860.7:c.-69_-65delinsGGAGT	ENSP00000348119.3:n.-69_-65delinsGGAGT
ENST00000402655.6:c.-69_-65delinsGGAGT	ENSP00000384238.2:n.-69_-65delinsGGAGT
ENST00000406884.6:c.-69_-65delinsGGAGT	ENSP00000384495.2:n.-69_-65delinsGGAGT
ENST00000408984.7:c.-69_-65delinsGGAGT	ENSP00000386161.3:n.-69_-65delinsGGAGT
ENST00000539474.6:c.-69_-65delinsGGAGT	ENSP00000445210.2:n.-69_-65delinsGGAGT
ENST00000562214.5:n.55_59delinsGGAGT
ENST00000566662.5:c.-69_-65delinsGGAGT	ENSP00000454331.1:n.-69_-65delinsGGAGT
ENST00000566780.5:c.-69_-65delinsGGAGT	ENSP00000457230.1:n.-69_-65delinsGGAGT
ENST00000569332.5:c.-69_-65delinsGGAGT	ENSP00000454788.1:n.-69_-65delinsGGAGT
ENST00000569818.1:c.-69_-65delinsGGAGT	ENSP00000454485.1:n.-69_-65delinsGGAGT
ENST00000627394.2:c.-69_-65delinsGGAGT	ENSP00000485925.1:n.-69_-65delinsGGAGT
NM_001291997.1:c.-343_-339delinsGGAGT	NP_001278926.1:n.-343_-339delinsGGAGT
NM_016373.3:c.-69_-65delinsGGAGT	NP_057457.1:n.-69_-65delinsGGAGT
NM_130791.3:c.-69_-65delinsGGAGT	NP_570607.1:n.-69_-65delinsGGAGT
NR_120435.1:n.298_302delinsGGAGT
NR_120436.1:n.298_302delinsGGAGT
XM_006721195.2:c.-69_-65delinsGGAGT	XP_006721258.1:n.-69_-65delinsGGAGT
XM_011523100.1:c.-69_-65delinsGGAGT	XP_011521402.1:n.-69_-65delinsGGAGT
XM_011523101.1:c.-69_-65delinsGGAGT	XP_011521403.1:n.-69_-65delinsGGAGT
XM_011523102.1:c.-69_-65delinsGGAGT	XP_011521404.1:n.-69_-65delinsGGAGT
XM_011523103.1:c.-69_-65delinsGGAGT	XP_011521405.1:n.-69_-65delinsGGAGT
XM_011523104.1:c.-69_-65delinsGGAGT	XP_011521406.1:n.-69_-65delinsGGAGT
XM_011523105.1:c.-69_-65delinsGGAGT	XP_011521407.1:n.-69_-65delinsGGAGT
XM_011523101.3:c.-69_-65delinsGGAGT	XP_011521403.1:n.-69_-65delinsGGAGT
XM_011523103.3:c.-69_-65delinsGGAGT	XP_011521405.1:n.-69_-65delinsGGAGT
XM_011523104.3:c.-69_-65delinsGGAGT	XP_011521406.1:n.-69_-65delinsGGAGT
XM_011523105.3:c.-69_-65delinsGGAGT	XP_011521407.1:n.-69_-65delinsGGAGT
XM_017023278.2:c.-69_-65delinsGGAGT	XP_016878767.1:n.-69_-65delinsGGAGT
NM_016373.4:c.-69_-65delinsGGAGT MANE Select	NP_057457.1:n.-69_-65delinsGGAGT
NM_001291997.2:c.-343_-339delinsGGAGT	NP_001278926.1:n.-343_-339delinsGGAGT
NM_130791.4:c.-69_-65delinsGGAGT	NP_570607.1:n.-69_-65delinsGGAGT
NR_120435.2:n.57_61delinsGGAGT
NR_120436.2:n.57_61delinsGGAGT
NM_130791.5:c.-69_-65delinsGGAGT	NP_570607.1:n.-69_-65delinsGGAGT
NR_120436.3:n.57_61delinsGGAGT