Canonical Allele Identifier: CA2234889062

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099750_78099751delinsAG , CM000678.2:g.78099750_78099751delinsAG	GRCh38
NC_000016.9:g.78133647_78133648delinsAG , CM000678.1:g.78133647_78133648delinsAG	GRCh37
NC_000016.8:g.76691148_76691149delinsAG	NCBI36
NG_011698.1:g.5097_5098delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-29_-28delinsAG	ENSP00000485925.2:n.-29_-28delinsAG
ENST00000682609.1:n.299_300delinsAG
ENST00000683286.1:n.299_300delinsAG
ENST00000683929.1:c.-29_-28delinsAG	ENSP00000507689.1:n.-29_-28delinsAG
ENST00000684070.1:n.301_302delinsAG
ENST00000684381.1:n.299_300delinsAG
ENST00000684452.1:n.299_300delinsAG
ENST00000684632.1:n.351_352delinsAG
ENST00000566780.6:c.-29_-28delinsAG MANE Select	ENSP00000457230.1:n.-29_-28delinsAG
ENST00000355860.7:c.-29_-28delinsAG	ENSP00000348119.3:n.-29_-28delinsAG
ENST00000402655.6:c.-29_-28delinsAG	ENSP00000384238.2:n.-29_-28delinsAG
ENST00000406884.6:c.-29_-28delinsAG	ENSP00000384495.2:n.-29_-28delinsAG
ENST00000408984.7:c.-29_-28delinsAG	ENSP00000386161.3:n.-29_-28delinsAG
ENST00000539474.6:c.-29_-28delinsAG	ENSP00000445210.2:n.-29_-28delinsAG
ENST00000561846.5:n.16_17delinsAG
ENST00000562214.5:n.95_96delinsAG
ENST00000565562.5:n.17_18delinsAG
ENST00000566662.5:c.-29_-28delinsAG	ENSP00000454331.1:n.-29_-28delinsAG
ENST00000566780.5:c.-29_-28delinsAG	ENSP00000457230.1:n.-29_-28delinsAG
ENST00000569332.5:c.-29_-28delinsAG	ENSP00000454788.1:n.-29_-28delinsAG
ENST00000569818.1:c.-29_-28delinsAG	ENSP00000454485.1:n.-29_-28delinsAG
ENST00000627394.2:c.-29_-28delinsAG	ENSP00000485925.1:n.-29_-28delinsAG
NM_001291997.1:c.-303_-302delinsAG	NP_001278926.1:n.-303_-302delinsAG
NM_016373.3:c.-29_-28delinsAG	NP_057457.1:n.-29_-28delinsAG
NM_130791.3:c.-29_-28delinsAG	NP_570607.1:n.-29_-28delinsAG
NR_120435.1:n.338_339delinsAG
NR_120436.1:n.338_339delinsAG
XM_006721195.2:c.-29_-28delinsAG	XP_006721258.1:n.-29_-28delinsAG
XM_011523100.1:c.-29_-28delinsAG	XP_011521402.1:n.-29_-28delinsAG
XM_011523101.1:c.-29_-28delinsAG	XP_011521403.1:n.-29_-28delinsAG
XM_011523102.1:c.-29_-28delinsAG	XP_011521404.1:n.-29_-28delinsAG
XM_011523103.1:c.-29_-28delinsAG	XP_011521405.1:n.-29_-28delinsAG
XM_011523104.1:c.-29_-28delinsAG	XP_011521406.1:n.-29_-28delinsAG
XM_011523105.1:c.-29_-28delinsAG	XP_011521407.1:n.-29_-28delinsAG
XM_011523101.3:c.-29_-28delinsAG	XP_011521403.1:n.-29_-28delinsAG
XM_011523103.3:c.-29_-28delinsAG	XP_011521405.1:n.-29_-28delinsAG
XM_011523104.3:c.-29_-28delinsAG	XP_011521406.1:n.-29_-28delinsAG
XM_011523105.3:c.-29_-28delinsAG	XP_011521407.1:n.-29_-28delinsAG
XM_017023278.2:c.-29_-28delinsAG	XP_016878767.1:n.-29_-28delinsAG
NM_016373.4:c.-29_-28delinsAG MANE Select	NP_057457.1:n.-29_-28delinsAG
NM_001291997.2:c.-303_-302delinsAG	NP_001278926.1:n.-303_-302delinsAG
NM_130791.4:c.-29_-28delinsAG	NP_570607.1:n.-29_-28delinsAG
NR_120435.2:n.97_98delinsAG
NR_120436.2:n.97_98delinsAG
NM_130791.5:c.-29_-28delinsAG	NP_570607.1:n.-29_-28delinsAG
NR_120436.3:n.97_98delinsAG