Canonical Allele Identifier: CA2234946454

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78224842_78224843delinsAT , CM000678.2:g.78224842_78224843delinsAT	GRCh38
NC_000016.9:g.78258739_78258740delinsAT , CM000678.1:g.78258739_78258740delinsAT	GRCh37
NC_000016.8:g.76816240_76816241delinsAT	NCBI36
NG_011698.1:g.130189_130190delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.516+60553_516+60554delinsAT	ENSP00000485925.2:n.516+60553_516+60554delinsAT
ENST00000683286.1:n.843+60553_843+60554delinsAT
ENST00000683929.1:c.516+60553_516+60554delinsAT	ENSP00000507689.1:n.516+60553_516+60554delinsAT
ENST00000684070.1:n.780+60553_780+60554delinsAT
ENST00000684632.1:n.895+60553_895+60554delinsAT
ENST00000566780.6:c.516+60553_516+60554delinsAT MANE Select	ENSP00000457230.1:n.516+60553_516+60554delinsAT
ENST00000355860.7:c.517-53761_517-53760delinsAT	ENSP00000348119.3:n.517-53761_517-53760delinsAT
ENST00000402655.6:c.409+109688_409+109689delinsAT	ENSP00000384238.2:n.409+109688_409+109689delinsAT
ENST00000406884.6:c.516+60553_516+60554delinsAT	ENSP00000384495.2:n.516+60553_516+60554delinsAT
ENST00000408984.7:c.516+60553_516+60554delinsAT	ENSP00000386161.3:n.516+60553_516+60554delinsAT
ENST00000539474.6:c.409+109688_409+109689delinsAT	ENSP00000445210.2:n.409+109688_409+109689delinsAT
ENST00000561846.5:n.561-55999_561-55998delinsAT
ENST00000562639.5:n.204+60553_204+60554delinsAT
ENST00000563358.5:n.624-53761_624-53760delinsAT
ENST00000565791.1:n.204-39627_204-39626delinsAT
ENST00000566662.5:c.*134+60553_*134+60554delinsAT	ENSP00000454331.1:n.*134+60553_*134+60554delinsAT
ENST00000566780.5:c.516+60553_516+60554delinsAT	ENSP00000457230.1:n.516+60553_516+60554delinsAT
ENST00000569332.5:c.*313+60553_*313+60554delinsAT	ENSP00000454788.1:n.*313+60553_*313+60554delinsAT
ENST00000627394.2:c.*314-53761_*314-53760delinsAT	ENSP00000485925.1:n.*314-53761_*314-53760delinsAT
NM_001291997.1:c.177+60553_177+60554delinsAT	NP_001278926.1:n.177+60553_177+60554delinsAT
NM_016373.3:c.516+60553_516+60554delinsAT	NP_057457.1:n.516+60553_516+60554delinsAT
NM_130791.3:c.517-53761_517-53760delinsAT	NP_570607.1:n.517-53761_517-53760delinsAT
NR_120436.1:n.997-53761_997-53760delinsAT
XM_006721195.2:c.516+60553_516+60554delinsAT	XP_006721258.1:n.516+60553_516+60554delinsAT
XM_011523100.1:c.516+60553_516+60554delinsAT	XP_011521402.1:n.516+60553_516+60554delinsAT
XM_011523101.1:c.516+60553_516+60554delinsAT	XP_011521403.1:n.516+60553_516+60554delinsAT
XM_011523102.1:c.516+60553_516+60554delinsAT	XP_011521404.1:n.516+60553_516+60554delinsAT
XM_011523103.1:c.516+60553_516+60554delinsAT	XP_011521405.1:n.516+60553_516+60554delinsAT
XM_011523104.1:c.516+60553_516+60554delinsAT	XP_011521406.1:n.516+60553_516+60554delinsAT
XM_011523105.1:c.517-3938_517-3937delinsAT	XP_011521407.1:n.517-3938_517-3937delinsAT
XM_011523101.3:c.516+60553_516+60554delinsAT	XP_011521403.1:n.516+60553_516+60554delinsAT
XM_011523103.3:c.516+60553_516+60554delinsAT	XP_011521405.1:n.516+60553_516+60554delinsAT
XM_011523104.3:c.516+60553_516+60554delinsAT	XP_011521406.1:n.516+60553_516+60554delinsAT
XM_011523105.3:c.517-3938_517-3937delinsAT	XP_011521407.1:n.517-3938_517-3937delinsAT
XM_017023278.2:c.516+60553_516+60554delinsAT	XP_016878767.1:n.516+60553_516+60554delinsAT
NM_016373.4:c.516+60553_516+60554delinsAT MANE Select	NP_057457.1:n.516+60553_516+60554delinsAT
NM_001291997.2:c.177+60553_177+60554delinsAT	NP_001278926.1:n.177+60553_177+60554delinsAT
NM_130791.4:c.517-53761_517-53760delinsAT	NP_570607.1:n.517-53761_517-53760delinsAT
NR_120436.2:n.756-53761_756-53760delinsAT
NM_130791.5:c.517-53761_517-53760delinsAT	NP_570607.1:n.517-53761_517-53760delinsAT
NR_120436.3:n.756-53761_756-53760delinsAT