Canonical Allele Identifier: CA396537065

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211663T>G , CM000678.2:g.79211663T>G	GRCh38
NC_000016.9:g.79245560T>G , CM000678.1:g.79245560T>G	GRCh37
NC_000016.8:g.77803061T>G	NCBI36
NG_011698.1:g.1117010T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*226T>G (WWOX)	ENSP00000507689.1:n.*226T>G
ENST00000566780.6:c.1112T>G (WWOX) MANE Select	ENSP00000457230.1:p.Leu371Arg
ENST00000402655.6:c.465T>G (WWOX)	ENSP00000384238.2:p.Ser155=
ENST00000406884.6:c.572T>G (WWOX)	ENSP00000384495.2:p.Leu191Arg
ENST00000539474.6:c.541T>G (WWOX)	ENSP00000445210.2:p.Trp181Gly
ENST00000566103.1:n.179T>G (WWOX)
ENST00000566780.5:c.1112T>G (WWOX)	ENSP00000457230.1:p.Leu371Arg
ENST00000569332.5:c.*909T>G (WWOX)	ENSP00000454788.1:n.*909T>G
NM_001291997.1:c.773T>G (WWOX)	NP_001278926.1:p.Leu258Arg
NM_016373.3:c.1112T>G (WWOX)	NP_057457.1:p.Leu371Arg
XM_011523100.1:c.1208T>G (WWOX)	XP_011521402.1:p.Leu403Arg
XM_011523103.3:c.*84T>G (WWOX)	XP_011521405.1:n.*84T>G
XM_017023279.1:c.198T>G (WWOX)	XP_016878768.1:p.Ser66=
XM_024450279.1:c.*1267A>C (MAF)	XP_024306047.1:n.*1267A>C
XR_001751902.2:n.4469A>C (MAF)
XR_002957802.1:n.4469A>C (MAF)
XR_002957803.1:n.4469A>C (MAF)
XR_002957804.1:n.4469A>C (MAF)
NM_016373.4:c.1112T>G (WWOX) MANE Select	NP_057457.1:p.Leu371Arg
NM_001291997.2:c.773T>G (WWOX)	NP_001278926.1:p.Leu258Arg