Canonical Allele Identifier: CA2235690777

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211868C= , CM000678.2:g.79211868C=	GRCh38
NC_000016.9:g.79245765C= , CM000678.1:g.79245765C=	GRCh37
NC_000016.8:g.77803266C=	NCBI36
NG_011698.1:g.1117215C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*431C= (WWOX)	ENSP00000507689.1:n.*431C=
ENST00000566780.6:c.*72C= (WWOX) MANE Select	ENSP00000457230.1:n.*72C=
ENST00000402655.6:c.670C= (WWOX)	ENSP00000384238.2:p.Pro224=
ENST00000406884.6:c.*72C= (WWOX)	ENSP00000384495.2:n.*72C=
ENST00000539474.6:c.*104C= (WWOX)	ENSP00000445210.2:n.*104C=
ENST00000566103.1:n.384C= (WWOX)
ENST00000566780.5:c.*72C= (WWOX)	ENSP00000457230.1:n.*72C=
ENST00000569332.5:c.*1114C= (WWOX)	ENSP00000454788.1:n.*1114C=
NM_001291997.1:c.*72C= (WWOX)	NP_001278926.1:n.*72C=
NM_016373.3:c.*72C= (WWOX)	NP_057457.1:n.*72C=
XM_011523100.1:c.*72C= (WWOX)	XP_011521402.1:n.*72C=
XM_011523103.3:c.*289C= (WWOX)	XP_011521405.1:n.*289C=
XM_017023279.1:c.403C= (WWOX)	XP_016878768.1:p.Pro135=
XM_024450279.1:c.*1062G= (MAF)	XP_024306047.1:n.*1062G=
XR_001751902.2:n.4264G= (MAF)
XR_002957802.1:n.4264G= (MAF)
XR_002957803.1:n.4264G= (MAF)
XR_002957804.1:n.4264G= (MAF)
NM_016373.4:c.*72C= (WWOX) MANE Select	NP_057457.1:n.*72C=
NM_001291997.2:c.*72C= (WWOX)	NP_001278926.1:n.*72C=