Canonical Allele Identifier: CA8183773

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211723A>G , CM000678.2:g.79211723A>G	GRCh38
NC_000016.9:g.79245620A>G , CM000678.1:g.79245620A>G	GRCh37
NC_000016.8:g.77803121A>G	NCBI36
NG_011698.1:g.1117070A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1172A>G (WWOX) MANE Select	NP_057457.1:p.Glu391Gly
ENST00000566780.6:c.1172A>G (WWOX) MANE Select	ENSP00000457230.1:p.Glu391Gly
NM_001291997.1:c.833A>G (WWOX)	NP_001278926.1:p.Glu278Gly
NM_001291997.2:c.833A>G (WWOX)	NP_001278926.1:p.Glu278Gly
NM_016373.3:c.1172A>G (WWOX)	NP_057457.1:p.Glu391Gly
ENST00000402655.6:c.525A>G (WWOX)	ENSP00000384238.2:p.Arg175=
ENST00000406884.6:c.632A>G (WWOX)	ENSP00000384495.2:p.Glu211Gly
ENST00000539474.6:c.601A>G (WWOX)	ENSP00000445210.2:p.Lys201Glu
ENST00000566103.1:n.239A>G (WWOX)
ENST00000566780.5:c.1172A>G (WWOX)	ENSP00000457230.1:p.Glu391Gly
ENST00000569332.5:c.*969A>G (WWOX)	ENSP00000454788.1:n.*969A>G
ENST00000683929.1:c.*286A>G (WWOX)	ENSP00000507689.1:n.*286A>G
XM_011523100.1:c.1268A>G (WWOX)	XP_011521402.1:p.Glu423Gly
XM_011523103.3:c.*144A>G (WWOX)	XP_011521405.1:n.*144A>G
XM_017023279.1:c.258A>G (WWOX)	XP_016878768.1:p.Arg86=
XM_024450279.1:c.*1207T>C (MAF)	XP_024306047.1:n.*1207T>C
XR_001751902.2:n.4409T>C (MAF)
XR_002957802.1:n.4409T>C (MAF)
XR_002957803.1:n.4409T>C (MAF)
XR_002957804.1:n.4409T>C (MAF)