Canonical Allele Identifier: CA2580092131

Gene: WWOX

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432539_78432540delinsCG , CM000678.2:g.78432539_78432540delinsCG	GRCh38
NC_000016.9:g.78466436_78466437delinsCG , CM000678.1:g.78466436_78466437delinsCG	GRCh37
NC_000016.8:g.77023937_77023938delinsCG	NCBI36
NG_011698.1:g.337886_337887delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.843_844delinsCG	ENSP00000485925.2:p.Pro282Ala
ENST00000683929.1:c.843_844delinsCG	ENSP00000507689.1:p.Pro282Ala
ENST00000684632.1:n.1222_1223delinsCG
ENST00000566780.6:c.843_844delinsCG MANE Select	ENSP00000457230.1:p.Pro282Ala
ENST00000402655.6:c.409+317385_409+317386delinsCG	ENSP00000384238.2:n.409+317385_409+317386delinsCG
ENST00000406884.6:c.516+268250_516+268251delinsCG	ENSP00000384495.2:n.516+268250_516+268251delinsCG
ENST00000408984.7:c.843_844delinsCG	ENSP00000386161.3:p.Pro282Ala
ENST00000539474.6:c.409+317385_409+317386delinsCG	ENSP00000445210.2:n.409+317385_409+317386delinsCG
ENST00000562639.5:n.531_532delinsCG
ENST00000566780.5:c.843_844delinsCG	ENSP00000457230.1:p.Pro282Ala
ENST00000569332.5:c.*640_*641delinsCG	ENSP00000454788.1:n.*640_*641delinsCG
ENST00000620008.1:c.237_238delinsCG	ENSP00000482648.1:p.Pro80Ala
NM_001291997.1:c.504_505delinsCG	NP_001278926.1:p.Pro169Ala
NM_016373.3:c.843_844delinsCG	NP_057457.1:p.Pro282Ala
XM_006721195.2:c.843_844delinsCG	XP_006721258.1:p.Pro282Ala
XM_011523100.1:c.843_844delinsCG	XP_011521402.1:p.Pro282Ala
XM_011523101.1:c.843_844delinsCG	XP_011521403.1:p.Pro282Ala
XM_011523102.1:c.843_844delinsCG	XP_011521404.1:p.Pro282Ala
XM_011523103.1:c.843_844delinsCG	XP_011521405.1:p.Pro282Ala
XM_011523104.1:c.843_844delinsCG	XP_011521406.1:p.Pro282Ala
XR_933765.1:n.3419-1727_3419-1726delinsCG
XM_011523101.3:c.843_844delinsCG	XP_011521403.1:p.Pro282Ala
XM_011523103.3:c.843_844delinsCG	XP_011521405.1:p.Pro282Ala
XM_011523104.3:c.843_844delinsCG	XP_011521406.1:p.Pro282Ala
NM_016373.4:c.843_844delinsCG MANE Select	NP_057457.1:p.Pro282Ala
NM_001291997.2:c.504_505delinsCG	NP_001278926.1:p.Pro169Ala