Canonical Allele Identifier: CA8183732

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211636G>A , CM000678.2:g.79211636G>A	GRCh38
NC_000016.9:g.79245533G>A , CM000678.1:g.79245533G>A	GRCh37
NC_000016.8:g.77803034G>A	NCBI36
NG_011698.1:g.1116983G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1085G>A (WWOX) MANE Select	NP_057457.1:p.Cys362Tyr
ENST00000566780.6:c.1085G>A (WWOX) MANE Select	ENSP00000457230.1:p.Cys362Tyr
NM_001291997.1:c.746G>A (WWOX)	NP_001278926.1:p.Cys249Tyr
NM_001291997.2:c.746G>A (WWOX)	NP_001278926.1:p.Cys249Tyr
NM_016373.3:c.1085G>A (WWOX)	NP_057457.1:p.Cys362Tyr
ENST00000402655.6:c.438G>A (WWOX)	ENSP00000384238.2:p.Leu146=
ENST00000406884.6:c.545G>A (WWOX)	ENSP00000384495.2:p.Cys182Tyr
ENST00000539474.6:c.514G>A (WWOX)	ENSP00000445210.2:p.Val172Met
ENST00000566103.1:n.152G>A (WWOX)
ENST00000566780.5:c.1085G>A (WWOX)	ENSP00000457230.1:p.Cys362Tyr
ENST00000569332.5:c.*882G>A (WWOX)	ENSP00000454788.1:n.*882G>A
ENST00000683929.1:c.*199G>A (WWOX)	ENSP00000507689.1:n.*199G>A
XM_011523100.1:c.1181G>A (WWOX)	XP_011521402.1:p.Cys394Tyr
XM_011523103.1:c.*57G>A (WWOX)	XP_011521405.1:n.*57G>A
XM_011523103.3:c.*57G>A (WWOX)	XP_011521405.1:n.*57G>A
XM_017023279.1:c.171G>A (WWOX)	XP_016878768.1:p.Leu57=
XM_024450279.1:c.*1294C>T (MAF)	XP_024306047.1:n.*1294C>T
XR_001751902.2:n.4496C>T (MAF)
XR_002957802.1:n.4496C>T (MAF)
XR_002957803.1:n.4496C>T (MAF)
XR_002957804.1:n.4496C>T (MAF)