Canonical Allele Identifier: CA396536933

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211614G>A , CM000678.2:g.79211614G>A	GRCh38
NC_000016.9:g.79245511G>A , CM000678.1:g.79245511G>A	GRCh37
NC_000016.8:g.77803012G>A	NCBI36
NG_011698.1:g.1116961G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*177G>A (WWOX)	ENSP00000507689.1:n.*177G>A
ENST00000566780.6:c.1063G>A (WWOX) MANE Select	ENSP00000457230.1:p.Gly355Arg
ENST00000402655.6:c.416G>A (WWOX)	ENSP00000384238.2:p.Gly139Glu
ENST00000406884.6:c.523G>A (WWOX)	ENSP00000384495.2:p.Gly175Arg
ENST00000539474.6:c.492G>A (WWOX)	ENSP00000445210.2:p.Arg164=
ENST00000566103.1:n.130G>A (WWOX)
ENST00000566780.5:c.1063G>A (WWOX)	ENSP00000457230.1:p.Gly355Arg
ENST00000569332.5:c.*860G>A (WWOX)	ENSP00000454788.1:n.*860G>A
NM_001291997.1:c.724G>A (WWOX)	NP_001278926.1:p.Gly242Arg
NM_016373.3:c.1063G>A (WWOX)	NP_057457.1:p.Gly355Arg
XM_011523100.1:c.1159G>A (WWOX)	XP_011521402.1:p.Gly387Arg
XM_011523103.1:c.*35G>A (WWOX)	XP_011521405.1:n.*35G>A
XM_011523103.3:c.*35G>A (WWOX)	XP_011521405.1:n.*35G>A
XM_017023279.1:c.149G>A (WWOX)	XP_016878768.1:p.Gly50Glu
XM_024450279.1:c.*1316C>T (MAF)	XP_024306047.1:n.*1316C>T
XR_001751902.2:n.4518C>T (MAF)
XR_002957802.1:n.4518C>T (MAF)
XR_002957803.1:n.4518C>T (MAF)
XR_002957804.1:n.4518C>T (MAF)
NM_016373.4:c.1063G>A (WWOX) MANE Select	NP_057457.1:p.Gly355Arg
NM_001291997.2:c.724G>A (WWOX)	NP_001278926.1:p.Gly242Arg