Canonical Allele Identifier: CA656671665

Gene: WWOX

Linked Data

• COSMIC: COSN19747877

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099757_78099758insG , CM000678.2:g.78099757_78099758insG	GRCh38
NC_000016.9:g.78133654_78133655insG , CM000678.1:g.78133654_78133655insG	GRCh37
NC_000016.8:g.76691155_76691156insG	NCBI36
NG_011698.1:g.5104_5105insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-22_-21insG	ENSP00000485925.2:n.-22_-21insG
ENST00000682609.1:n.306_307insG
ENST00000683286.1:n.306_307insG
ENST00000683929.1:c.-22_-21insG	ENSP00000507689.1:n.-22_-21insG
ENST00000684070.1:n.308_309insG
ENST00000684381.1:n.306_307insG
ENST00000684452.1:n.306_307insG
ENST00000684632.1:n.358_359insG
ENST00000566780.6:c.-22_-21insG MANE Select	ENSP00000457230.1:n.-22_-21insG
ENST00000355860.7:c.-22_-21insG	ENSP00000348119.3:n.-22_-21insG
ENST00000402655.6:c.-22_-21insG	ENSP00000384238.2:n.-22_-21insG
ENST00000406884.6:c.-22_-21insG	ENSP00000384495.2:n.-22_-21insG
ENST00000408984.7:c.-22_-21insG	ENSP00000386161.3:n.-22_-21insG
ENST00000539474.6:c.-22_-21insG	ENSP00000445210.2:n.-22_-21insG
ENST00000561846.5:n.23_24insG
ENST00000562214.5:n.102_103insG
ENST00000565562.5:n.24_25insG
ENST00000566662.5:c.-22_-21insG	ENSP00000454331.1:n.-22_-21insG
ENST00000566780.5:c.-22_-21insG	ENSP00000457230.1:n.-22_-21insG
ENST00000569332.5:c.-22_-21insG	ENSP00000454788.1:n.-22_-21insG
ENST00000569818.1:c.-22_-21insG	ENSP00000454485.1:n.-22_-21insG
ENST00000627394.2:c.-22_-21insG	ENSP00000485925.1:n.-22_-21insG
NM_001291997.1:c.-296_-295insG	NP_001278926.1:n.-296_-295insG
NM_016373.3:c.-22_-21insG	NP_057457.1:n.-22_-21insG
NM_130791.3:c.-22_-21insG	NP_570607.1:n.-22_-21insG
NR_120435.1:n.345_346insG
NR_120436.1:n.345_346insG
XM_006721195.2:c.-22_-21insG	XP_006721258.1:n.-22_-21insG
XM_011523100.1:c.-22_-21insG	XP_011521402.1:n.-22_-21insG
XM_011523101.1:c.-22_-21insG	XP_011521403.1:n.-22_-21insG
XM_011523102.1:c.-22_-21insG	XP_011521404.1:n.-22_-21insG
XM_011523103.1:c.-22_-21insG	XP_011521405.1:n.-22_-21insG
XM_011523104.1:c.-22_-21insG	XP_011521406.1:n.-22_-21insG
XM_011523105.1:c.-22_-21insG	XP_011521407.1:n.-22_-21insG
XM_011523101.3:c.-22_-21insG	XP_011521403.1:n.-22_-21insG
XM_011523103.3:c.-22_-21insG	XP_011521405.1:n.-22_-21insG
XM_011523104.3:c.-22_-21insG	XP_011521406.1:n.-22_-21insG
XM_011523105.3:c.-22_-21insG	XP_011521407.1:n.-22_-21insG
XM_017023278.2:c.-22_-21insG	XP_016878767.1:n.-22_-21insG
NM_016373.4:c.-22_-21insG MANE Select	NP_057457.1:n.-22_-21insG
NM_001291997.2:c.-296_-295insG	NP_001278926.1:n.-296_-295insG
NM_130791.4:c.-22_-21insG	NP_570607.1:n.-22_-21insG
NR_120435.2:n.104_105insG
NR_120436.2:n.104_105insG
NM_130791.5:c.-22_-21insG	NP_570607.1:n.-22_-21insG
NR_120436.3:n.104_105insG