Canonical Allele Identifier: CA2235073056

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432613_78432614delinsAG , CM000678.2:g.78432613_78432614delinsAG	GRCh38
NC_000016.9:g.78466510_78466511delinsAG , CM000678.1:g.78466510_78466511delinsAG	GRCh37
NC_000016.8:g.77024011_77024012delinsAG	NCBI36
NG_011698.1:g.337960_337961delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.917_918delinsAG	ENSP00000485925.2:p.Glu306=
ENST00000683929.1:c.917_918delinsAG	ENSP00000507689.1:p.Glu306=
ENST00000684632.1:n.1296_1297delinsAG
ENST00000566780.6:c.917_918delinsAG MANE Select	ENSP00000457230.1:p.Glu306=
ENST00000402655.6:c.409+317459_409+317460delinsAG	ENSP00000384238.2:n.409+317459_409+317460...
ENST00000406884.6:c.516+268324_516+268325delinsAG	ENSP00000384495.2:n.516+268324_516+268325...
ENST00000408984.7:c.917_918delinsAG	ENSP00000386161.3:p.Glu306=
ENST00000539474.6:c.409+317459_409+317460delinsAG	ENSP00000445210.2:n.409+317459_409+317460...
ENST00000566780.5:c.917_918delinsAG	ENSP00000457230.1:p.Glu306=
ENST00000569332.5:c.*714_*715delinsAG	ENSP00000454788.1:n.*714_*715delinsAG
ENST00000620008.1:c.311_312delinsAG	ENSP00000482648.1:p.Glu104=
NM_001291997.1:c.578_579delinsAG	NP_001278926.1:p.Glu193=
NM_016373.3:c.917_918delinsAG	NP_057457.1:p.Glu306=
XM_006721195.2:c.917_918delinsAG	XP_006721258.1:p.Glu306=
XM_011523100.1:c.917_918delinsAG	XP_011521402.1:p.Glu306=
XM_011523101.1:c.917_918delinsAG	XP_011521403.1:p.Glu306=
XM_011523102.1:c.917_918delinsAG	XP_011521404.1:p.Glu306=
XM_011523103.1:c.917_918delinsAG	XP_011521405.1:p.Glu306=
XM_011523104.1:c.917_918delinsAG	XP_011521406.1:p.Glu306=
XR_933765.1:n.3418+1706_3418+1707delinsCT
XM_011523101.3:c.917_918delinsAG	XP_011521403.1:p.Glu306=
XM_011523103.3:c.917_918delinsAG	XP_011521405.1:p.Glu306=
XM_011523104.3:c.917_918delinsAG	XP_011521406.1:p.Glu306=
NM_016373.4:c.917_918delinsAG MANE Select	NP_057457.1:p.Glu306=
NM_001291997.2:c.578_579delinsAG	NP_001278926.1:p.Glu193=