Canonical Allele Identifier: CA2235072722

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432526T= , CM000678.2:g.78432526T=	GRCh38
NC_000016.9:g.78466423T= , CM000678.1:g.78466423T=	GRCh37
NC_000016.8:g.77023924T=	NCBI36
NG_011698.1:g.337873T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.830T=	ENSP00000485925.2:p.Phe277=
ENST00000683929.1:c.830T=	ENSP00000507689.1:p.Phe277=
ENST00000684632.1:n.1209T=
ENST00000566780.6:c.830T= MANE Select	ENSP00000457230.1:p.Phe277=
ENST00000402655.6:c.409+317372T=	ENSP00000384238.2:n.409+317372T=
ENST00000406884.6:c.516+268237T=	ENSP00000384495.2:n.516+268237T=
ENST00000408984.7:c.830T=	ENSP00000386161.3:p.Phe277=
ENST00000539474.6:c.409+317372T=	ENSP00000445210.2:n.409+317372T=
ENST00000562639.5:n.518T=
ENST00000566780.5:c.830T=	ENSP00000457230.1:p.Phe277=
ENST00000569332.5:c.*627T=	ENSP00000454788.1:n.*627T=
ENST00000620008.1:c.224T=	ENSP00000482648.1:p.Phe75=
NM_001291997.1:c.491T=	NP_001278926.1:p.Phe164=
NM_016373.3:c.830T=	NP_057457.1:p.Phe277=
XM_006721195.2:c.830T=	XP_006721258.1:p.Phe277=
XM_011523100.1:c.830T=	XP_011521402.1:p.Phe277=
XM_011523101.1:c.830T=	XP_011521403.1:p.Phe277=
XM_011523102.1:c.830T=	XP_011521404.1:p.Phe277=
XM_011523103.1:c.830T=	XP_011521405.1:p.Phe277=
XM_011523104.1:c.830T=	XP_011521406.1:p.Phe277=
XR_933765.1:n.3419-1713A=
XM_011523101.3:c.830T=	XP_011521403.1:p.Phe277=
XM_011523103.3:c.830T=	XP_011521405.1:p.Phe277=
XM_011523104.3:c.830T=	XP_011521406.1:p.Phe277=
NM_016373.4:c.830T= MANE Select	NP_057457.1:p.Phe277=
NM_001291997.2:c.491T=	NP_001278926.1:p.Phe164=