Canonical Allele Identifier: CA396537175

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211708C>T , CM000678.2:g.79211708C>T	GRCh38
NC_000016.9:g.79245605C>T , CM000678.1:g.79245605C>T	GRCh37
NC_000016.8:g.77803106C>T	NCBI36
NG_011698.1:g.1117055C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*271C>T (WWOX)	ENSP00000507689.1:n.*271C>T
ENST00000566780.6:c.1157C>T (WWOX) MANE Select	ENSP00000457230.1:p.Pro386Leu
ENST00000402655.6:c.510C>T (WWOX)	ENSP00000384238.2:p.Thr170=
ENST00000406884.6:c.617C>T (WWOX)	ENSP00000384495.2:p.Pro206Leu
ENST00000539474.6:c.586C>T (WWOX)	ENSP00000445210.2:p.Gln196Ter
ENST00000566103.1:n.224C>T (WWOX)
ENST00000566780.5:c.1157C>T (WWOX)	ENSP00000457230.1:p.Pro386Leu
ENST00000569332.5:c.*954C>T (WWOX)	ENSP00000454788.1:n.*954C>T
NM_001291997.1:c.818C>T (WWOX)	NP_001278926.1:p.Pro273Leu
NM_016373.3:c.1157C>T (WWOX)	NP_057457.1:p.Pro386Leu
XM_011523100.1:c.1253C>T (WWOX)	XP_011521402.1:p.Pro418Leu
XM_011523103.3:c.*129C>T (WWOX)	XP_011521405.1:n.*129C>T
XM_017023279.1:c.243C>T (WWOX)	XP_016878768.1:p.Thr81=
XM_024450279.1:c.*1222G>A (MAF)	XP_024306047.1:n.*1222G>A
XR_001751902.2:n.4424G>A (MAF)
XR_002957802.1:n.4424G>A (MAF)
XR_002957803.1:n.4424G>A (MAF)
XR_002957804.1:n.4424G>A (MAF)
NM_016373.4:c.1157C>T (WWOX) MANE Select	NP_057457.1:p.Pro386Leu
NM_001291997.2:c.818C>T (WWOX)	NP_001278926.1:p.Pro273Leu