Canonical Allele Identifier: CA2235072777

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432540C= , CM000678.2:g.78432540C=	GRCh38
NC_000016.9:g.78466437C= , CM000678.1:g.78466437C=	GRCh37
NC_000016.8:g.77023938C=	NCBI36
NG_011698.1:g.337887C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.844C= MANE Select	NP_057457.1:p.Pro282=
ENST00000566780.6:c.844C= MANE Select	ENSP00000457230.1:p.Pro282=
NM_001291997.1:c.505C=	NP_001278926.1:p.Pro169=
NM_001291997.2:c.505C=	NP_001278926.1:p.Pro169=
NM_016373.3:c.844C=	NP_057457.1:p.Pro282=
ENST00000402655.6:c.409+317386C=	ENSP00000384238.2:n.409+317386C=
ENST00000406884.6:c.516+268251C=	ENSP00000384495.2:n.516+268251C=
ENST00000408984.7:c.844C=	ENSP00000386161.3:p.Pro282=
ENST00000539474.6:c.409+317386C=	ENSP00000445210.2:n.409+317386C=
ENST00000562639.5:n.532C=
ENST00000566780.5:c.844C=	ENSP00000457230.1:p.Pro282=
ENST00000569332.5:c.*641C=	ENSP00000454788.1:n.*641C=
ENST00000620008.1:c.238C=	ENSP00000482648.1:p.Pro80=
ENST00000627394.3:c.844C=	ENSP00000485925.2:p.Pro282=
ENST00000683929.1:c.844C=	ENSP00000507689.1:p.Pro282=
ENST00000684632.1:n.1223C=
XM_006721195.2:c.844C=	XP_006721258.1:p.Pro282=
XM_011523100.1:c.844C=	XP_011521402.1:p.Pro282=
XM_011523101.1:c.844C=	XP_011521403.1:p.Pro282=
XM_011523101.3:c.844C=	XP_011521403.1:p.Pro282=
XM_011523102.1:c.844C=	XP_011521404.1:p.Pro282=
XM_011523103.1:c.844C=	XP_011521405.1:p.Pro282=
XM_011523103.3:c.844C=	XP_011521405.1:p.Pro282=
XM_011523104.1:c.844C=	XP_011521406.1:p.Pro282=
XM_011523104.3:c.844C=	XP_011521406.1:p.Pro282=
XR_933765.1:n.3419-1727G=