Canonical Allele Identifier: CA396537217

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211727G>T , CM000678.2:g.79211727G>T	GRCh38
NC_000016.9:g.79245624G>T , CM000678.1:g.79245624G>T	GRCh37
NC_000016.8:g.77803125G>T	NCBI36
NG_011698.1:g.1117074G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1176G>T (WWOX) MANE Select	NP_057457.1:p.Glu392Asp
ENST00000566780.6:c.1176G>T (WWOX) MANE Select	ENSP00000457230.1:p.Glu392Asp
NM_001291997.1:c.837G>T (WWOX)	NP_001278926.1:p.Glu279Asp
NM_001291997.2:c.837G>T (WWOX)	NP_001278926.1:p.Glu279Asp
NM_016373.3:c.1176G>T (WWOX)	NP_057457.1:p.Glu392Asp
ENST00000402655.6:c.529G>T (WWOX)	ENSP00000384238.2:p.Asp177Tyr
ENST00000406884.6:c.636G>T (WWOX)	ENSP00000384495.2:p.Glu212Asp
ENST00000539474.6:c.605G>T (WWOX)	ENSP00000445210.2:p.Arg202Ile
ENST00000566103.1:n.243G>T (WWOX)
ENST00000566780.5:c.1176G>T (WWOX)	ENSP00000457230.1:p.Glu392Asp
ENST00000569332.5:c.*973G>T (WWOX)	ENSP00000454788.1:n.*973G>T
ENST00000683929.1:c.*290G>T (WWOX)	ENSP00000507689.1:n.*290G>T
XM_011523100.1:c.1272G>T (WWOX)	XP_011521402.1:p.Glu424Asp
XM_011523103.3:c.*148G>T (WWOX)	XP_011521405.1:n.*148G>T
XM_017023279.1:c.262G>T (WWOX)	XP_016878768.1:p.Asp88Tyr
XM_024450279.1:c.*1203C>A (MAF)	XP_024306047.1:n.*1203C>A
XR_001751902.2:n.4405C>A (MAF)
XR_002957802.1:n.4405C>A (MAF)
XR_002957803.1:n.4405C>A (MAF)
XR_002957804.1:n.4405C>A (MAF)