Canonical Allele Identifier: CA8183748

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211676C>T , CM000678.2:g.79211676C>T	GRCh38
NC_000016.9:g.79245573C>T , CM000678.1:g.79245573C>T	GRCh37
NC_000016.8:g.77803074C>T	NCBI36
NG_011698.1:g.1117023C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*239C>T (WWOX)	ENSP00000507689.1:n.*239C>T
ENST00000566780.6:c.1125C>T (WWOX) MANE Select	ENSP00000457230.1:p.Tyr375=
ENST00000402655.6:c.478C>T (WWOX)	ENSP00000384238.2:p.Leu160Phe
ENST00000406884.6:c.585C>T (WWOX)	ENSP00000384495.2:p.Tyr195=
ENST00000539474.6:c.554C>T (WWOX)	ENSP00000445210.2:p.Thr185Ile
ENST00000566103.1:n.192C>T (WWOX)
ENST00000566780.5:c.1125C>T (WWOX)	ENSP00000457230.1:p.Tyr375=
ENST00000569332.5:c.*922C>T (WWOX)	ENSP00000454788.1:n.*922C>T
NM_001291997.1:c.786C>T (WWOX)	NP_001278926.1:p.Tyr262=
NM_016373.3:c.1125C>T (WWOX)	NP_057457.1:p.Tyr375=
XM_011523100.1:c.1221C>T (WWOX)	XP_011521402.1:p.Tyr407=
XM_011523103.3:c.*97C>T (WWOX)	XP_011521405.1:n.*97C>T
XM_017023279.1:c.211C>T (WWOX)	XP_016878768.1:p.Leu71Phe
XM_024450279.1:c.*1254G>A (MAF)	XP_024306047.1:n.*1254G>A
XR_001751902.2:n.4456G>A (MAF)
XR_002957802.1:n.4456G>A (MAF)
XR_002957803.1:n.4456G>A (MAF)
XR_002957804.1:n.4456G>A (MAF)
NM_016373.4:c.1125C>T (WWOX) MANE Select	NP_057457.1:p.Tyr375=
NM_001291997.2:c.786C>T (WWOX)	NP_001278926.1:p.Tyr262=