Canonical Allele Identifier: CA2235690612

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211666G= , CM000678.2:g.79211666G=	GRCh38
NC_000016.9:g.79245563G= , CM000678.1:g.79245563G=	GRCh37
NC_000016.8:g.77803064G=	NCBI36
NG_011698.1:g.1117013G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1115G= (WWOX) MANE Select	NP_057457.1:p.Gly372=
ENST00000566780.6:c.1115G= (WWOX) MANE Select	ENSP00000457230.1:p.Gly372=
NM_001291997.1:c.776G= (WWOX)	NP_001278926.1:p.Gly259=
NM_001291997.2:c.776G= (WWOX)	NP_001278926.1:p.Gly259=
NM_016373.3:c.1115G= (WWOX)	NP_057457.1:p.Gly372=
ENST00000402655.6:c.468G= (WWOX)	ENSP00000384238.2:p.Gly156=
ENST00000406884.6:c.575G= (WWOX)	ENSP00000384495.2:p.Gly192=
ENST00000539474.6:c.544G= (WWOX)	ENSP00000445210.2:p.Glu182=
ENST00000566103.1:n.182G= (WWOX)
ENST00000566780.5:c.1115G= (WWOX)	ENSP00000457230.1:p.Gly372=
ENST00000569332.5:c.*912G= (WWOX)	ENSP00000454788.1:n.*912G=
ENST00000683929.1:c.*229G= (WWOX)	ENSP00000507689.1:n.*229G=
XM_011523100.1:c.1211G= (WWOX)	XP_011521402.1:p.Gly404=
XM_011523103.3:c.*87G= (WWOX)	XP_011521405.1:n.*87G=
XM_017023279.1:c.201G= (WWOX)	XP_016878768.1:p.Gly67=
XM_024450279.1:c.*1264C= (MAF)	XP_024306047.1:n.*1264C=
XR_001751902.2:n.4466C= (MAF)
XR_002957802.1:n.4466C= (MAF)
XR_002957803.1:n.4466C= (MAF)
XR_002957804.1:n.4466C= (MAF)