Canonical Allele Identifier: CA2235690611

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211665G= , CM000678.2:g.79211665G=	GRCh38
NC_000016.9:g.79245562G= , CM000678.1:g.79245562G=	GRCh37
NC_000016.8:g.77803063G=	NCBI36
NG_011698.1:g.1117012G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1114G= (WWOX) MANE Select	NP_057457.1:p.Gly372=
ENST00000566780.6:c.1114G= (WWOX) MANE Select	ENSP00000457230.1:p.Gly372=
NM_001291997.1:c.775G= (WWOX)	NP_001278926.1:p.Gly259=
NM_001291997.2:c.775G= (WWOX)	NP_001278926.1:p.Gly259=
NM_016373.3:c.1114G= (WWOX)	NP_057457.1:p.Gly372=
ENST00000402655.6:c.467G= (WWOX)	ENSP00000384238.2:p.Gly156=
ENST00000406884.6:c.574G= (WWOX)	ENSP00000384495.2:p.Gly192=
ENST00000539474.6:c.543G= (WWOX)	ENSP00000445210.2:p.Trp181=
ENST00000566103.1:n.181G= (WWOX)
ENST00000566780.5:c.1114G= (WWOX)	ENSP00000457230.1:p.Gly372=
ENST00000569332.5:c.*911G= (WWOX)	ENSP00000454788.1:n.*911G=
ENST00000683929.1:c.*228G= (WWOX)	ENSP00000507689.1:n.*228G=
XM_011523100.1:c.1210G= (WWOX)	XP_011521402.1:p.Gly404=
XM_011523103.3:c.*86G= (WWOX)	XP_011521405.1:n.*86G=
XM_017023279.1:c.200G= (WWOX)	XP_016878768.1:p.Gly67=
XM_024450279.1:c.*1265C= (MAF)	XP_024306047.1:n.*1265C=
XR_001751902.2:n.4467C= (MAF)
XR_002957802.1:n.4467C= (MAF)
XR_002957803.1:n.4467C= (MAF)
XR_002957804.1:n.4467C= (MAF)