Canonical Allele Identifier: CA284131520

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211729C>G , CM000678.2:g.79211729C>G	GRCh38
NC_000016.9:g.79245626C>G , CM000678.1:g.79245626C>G	GRCh37
NC_000016.8:g.77803127C>G	NCBI36
NG_011698.1:g.1117076C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*292C>G (WWOX)	ENSP00000507689.1:n.*292C>G
ENST00000566780.6:c.1178C>G (WWOX) MANE Select	ENSP00000457230.1:p.Thr393Arg
ENST00000402655.6:c.531C>G (WWOX)	ENSP00000384238.2:p.Asp177Glu
ENST00000406884.6:c.638C>G (WWOX)	ENSP00000384495.2:p.Thr213Arg
ENST00000539474.6:c.607C>G (WWOX)	ENSP00000445210.2:p.Arg203Gly
ENST00000566103.1:n.245C>G (WWOX)
ENST00000566780.5:c.1178C>G (WWOX)	ENSP00000457230.1:p.Thr393Arg
ENST00000569332.5:c.*975C>G (WWOX)	ENSP00000454788.1:n.*975C>G
NM_001291997.1:c.839C>G (WWOX)	NP_001278926.1:p.Thr280Arg
NM_016373.3:c.1178C>G (WWOX)	NP_057457.1:p.Thr393Arg
XM_011523100.1:c.1274C>G (WWOX)	XP_011521402.1:p.Thr425Arg
XM_011523103.3:c.*150C>G (WWOX)	XP_011521405.1:n.*150C>G
XM_017023279.1:c.264C>G (WWOX)	XP_016878768.1:p.Asp88Glu
XM_024450279.1:c.*1201G>C (MAF)	XP_024306047.1:n.*1201G>C
XR_001751902.2:n.4403G>C (MAF)
XR_002957802.1:n.4403G>C (MAF)
XR_002957803.1:n.4403G>C (MAF)
XR_002957804.1:n.4403G>C (MAF)
NM_016373.4:c.1178C>G (WWOX) MANE Select	NP_057457.1:p.Thr393Arg
NM_001291997.2:c.839C>G (WWOX)	NP_001278926.1:p.Thr280Arg