Canonical Allele Identifier: CA284131157

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211608C>T , CM000678.2:g.79211608C>T	GRCh38
NC_000016.9:g.79245505C>T , CM000678.1:g.79245505C>T	GRCh37
NC_000016.8:g.77803006C>T	NCBI36
NG_011698.1:g.1116955C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1057C>T (WWOX) MANE Select	NP_057457.1:p.Gln353Ter
ENST00000566780.6:c.1057C>T (WWOX) MANE Select	ENSP00000457230.1:p.Gln353Ter
NM_001291997.1:c.718C>T (WWOX)	NP_001278926.1:p.Gln240Ter
NM_001291997.2:c.718C>T (WWOX)	NP_001278926.1:p.Gln240Ter
NM_016373.3:c.1057C>T (WWOX)	NP_057457.1:p.Gln353Ter
ENST00000402655.6:c.410C>T (WWOX)	ENSP00000384238.2:p.Ala137Val
ENST00000406884.6:c.517C>T (WWOX)	ENSP00000384495.2:p.Gln173Ter
ENST00000539474.6:c.486C>T (WWOX)	ENSP00000445210.2:p.Ile162=
ENST00000566103.1:n.124C>T (WWOX)
ENST00000566780.5:c.1057C>T (WWOX)	ENSP00000457230.1:p.Gln353Ter
ENST00000569332.5:c.*854C>T (WWOX)	ENSP00000454788.1:n.*854C>T
ENST00000683929.1:c.*171C>T (WWOX)	ENSP00000507689.1:n.*171C>T
XM_011523100.1:c.1153C>T (WWOX)	XP_011521402.1:p.Gln385Ter
XM_011523103.1:c.*29C>T (WWOX)	XP_011521405.1:n.*29C>T
XM_011523103.3:c.*29C>T (WWOX)	XP_011521405.1:n.*29C>T
XM_017023279.1:c.143C>T (WWOX)	XP_016878768.1:p.Ala48Val
XM_024450279.1:c.*1322G>A (MAF)	XP_024306047.1:n.*1322G>A
XR_001751902.2:n.4524G>A (MAF)
XR_002957802.1:n.4524G>A (MAF)
XR_002957803.1:n.4524G>A (MAF)
XR_002957804.1:n.4524G>A (MAF)