Canonical Allele Identifier: CA2235690929

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79212059C= , CM000678.2:g.79212059C=	GRCh38
NC_000016.9:g.79245956C= , CM000678.1:g.79245956C=	GRCh37
NC_000016.8:g.77803457C=	NCBI36
NG_011698.1:g.1117406C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.*263C= (WWOX) MANE Select	NP_057457.1:n.*263C=
ENST00000566780.6:c.*263C= (WWOX) MANE Select	ENSP00000457230.1:n.*263C=
NM_001291997.1:c.*263C= (WWOX)	NP_001278926.1:n.*263C=
NM_001291997.2:c.*263C= (WWOX)	NP_001278926.1:n.*263C=
NM_016373.3:c.*263C= (WWOX)	NP_057457.1:n.*263C=
ENST00000402655.6:c.861C= (WWOX)	ENSP00000384238.2:p.Cys287=
ENST00000406884.6:c.*263C= (WWOX)	ENSP00000384495.2:n.*263C=
ENST00000539474.6:c.*295C= (WWOX)	ENSP00000445210.2:n.*295C=
ENST00000566103.1:n.575C= (WWOX)
ENST00000566780.5:c.*263C= (WWOX)	ENSP00000457230.1:n.*263C=
ENST00000569332.5:c.*1305C= (WWOX)	ENSP00000454788.1:n.*1305C=
ENST00000683929.1:c.*622C= (WWOX)	ENSP00000507689.1:n.*622C=
XM_011523100.1:c.*263C= (WWOX)	XP_011521402.1:n.*263C=
XM_011523103.3:c.*480C= (WWOX)	XP_011521405.1:n.*480C=
XM_017023279.1:c.594C= (WWOX)	XP_016878768.1:p.Cys198=
XM_024450279.1:c.*871G= (MAF)	XP_024306047.1:n.*871G=
XR_001751902.2:n.4073G= (MAF)
XR_002957802.1:n.4073G= (MAF)
XR_002957803.1:n.4073G= (MAF)
XR_002957804.1:n.4073G= (MAF)