Canonical Allele Identifier: CA396536974

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211628C>G , CM000678.2:g.79211628C>G	GRCh38
NC_000016.9:g.79245525C>G , CM000678.1:g.79245525C>G	GRCh37
NC_000016.8:g.77803026C>G	NCBI36
NG_011698.1:g.1116975C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*191C>G (WWOX)	ENSP00000507689.1:n.*191C>G
ENST00000566780.6:c.1077C>G (WWOX) MANE Select	ENSP00000457230.1:p.Thr359=
ENST00000402655.6:c.430C>G (WWOX)	ENSP00000384238.2:p.Arg144Gly
ENST00000406884.6:c.537C>G (WWOX)	ENSP00000384495.2:p.Thr179=
ENST00000539474.6:c.506C>G (WWOX)	ENSP00000445210.2:p.Pro169Arg
ENST00000566103.1:n.144C>G (WWOX)
ENST00000566780.5:c.1077C>G (WWOX)	ENSP00000457230.1:p.Thr359=
ENST00000569332.5:c.*874C>G (WWOX)	ENSP00000454788.1:n.*874C>G
NM_001291997.1:c.738C>G (WWOX)	NP_001278926.1:p.Thr246=
NM_016373.3:c.1077C>G (WWOX)	NP_057457.1:p.Thr359=
XM_011523100.1:c.1173C>G (WWOX)	XP_011521402.1:p.Thr391=
XM_011523103.1:c.*49C>G (WWOX)	XP_011521405.1:n.*49C>G
XM_011523103.3:c.*49C>G (WWOX)	XP_011521405.1:n.*49C>G
XM_017023279.1:c.163C>G (WWOX)	XP_016878768.1:p.Arg55Gly
XM_024450279.1:c.*1302G>C (MAF)	XP_024306047.1:n.*1302G>C
XR_001751902.2:n.4504G>C (MAF)
XR_002957802.1:n.4504G>C (MAF)
XR_002957803.1:n.4504G>C (MAF)
XR_002957804.1:n.4504G>C (MAF)
NM_016373.4:c.1077C>G (WWOX) MANE Select	NP_057457.1:p.Thr359=
NM_001291997.2:c.738C>G (WWOX)	NP_001278926.1:p.Thr246=