Canonical Allele Identifier: CA8183833

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211829G>A , CM000678.2:g.79211829G>A	GRCh38
NC_000016.9:g.79245726G>A , CM000678.1:g.79245726G>A	GRCh37
NC_000016.8:g.77803227G>A	NCBI36
NG_011698.1:g.1117176G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.*33G>A (WWOX) MANE Select	NP_057457.1:n.*33G>A
ENST00000566780.6:c.*33G>A (WWOX) MANE Select	ENSP00000457230.1:n.*33G>A
NM_001291997.1:c.*33G>A (WWOX)	NP_001278926.1:n.*33G>A
NM_001291997.2:c.*33G>A (WWOX)	NP_001278926.1:n.*33G>A
NM_016373.3:c.*33G>A (WWOX)	NP_057457.1:n.*33G>A
ENST00000402655.6:c.631G>A (WWOX)	ENSP00000384238.2:p.Ala211Thr
ENST00000406884.6:c.*33G>A (WWOX)	ENSP00000384495.2:n.*33G>A
ENST00000539474.6:c.*65G>A (WWOX)	ENSP00000445210.2:n.*65G>A
ENST00000566103.1:n.345G>A (WWOX)
ENST00000566780.5:c.*33G>A (WWOX)	ENSP00000457230.1:n.*33G>A
ENST00000569332.5:c.*1075G>A (WWOX)	ENSP00000454788.1:n.*1075G>A
ENST00000683929.1:c.*392G>A (WWOX)	ENSP00000507689.1:n.*392G>A
XM_011523100.1:c.*33G>A (WWOX)	XP_011521402.1:n.*33G>A
XM_011523103.3:c.*250G>A (WWOX)	XP_011521405.1:n.*250G>A
XM_017023279.1:c.364G>A (WWOX)	XP_016878768.1:p.Ala122Thr
XM_024450279.1:c.*1101C>T (MAF)	XP_024306047.1:n.*1101C>T
XR_001751902.2:n.4303C>T (MAF)
XR_002957802.1:n.4303C>T (MAF)
XR_002957803.1:n.4303C>T (MAF)
XR_002957804.1:n.4303C>T (MAF)