Canonical Allele Identifier: CA396537114

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211682C>G , CM000678.2:g.79211682C>G	GRCh38
NC_000016.9:g.79245579C>G , CM000678.1:g.79245579C>G	GRCh37
NC_000016.8:g.77803080C>G	NCBI36
NG_011698.1:g.1117029C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1131C>G (WWOX) MANE Select	NP_057457.1:p.Asn377Lys
ENST00000566780.6:c.1131C>G (WWOX) MANE Select	ENSP00000457230.1:p.Asn377Lys
NM_001291997.1:c.792C>G (WWOX)	NP_001278926.1:p.Asn264Lys
NM_001291997.2:c.792C>G (WWOX)	NP_001278926.1:p.Asn264Lys
NM_016373.3:c.1131C>G (WWOX)	NP_057457.1:p.Asn377Lys
ENST00000402655.6:c.484C>G (WWOX)	ENSP00000384238.2:p.Gln162Glu
ENST00000406884.6:c.591C>G (WWOX)	ENSP00000384495.2:p.Asn197Lys
ENST00000539474.6:c.560C>G (WWOX)	ENSP00000445210.2:p.Thr187Arg
ENST00000566103.1:n.198C>G (WWOX)
ENST00000566780.5:c.1131C>G (WWOX)	ENSP00000457230.1:p.Asn377Lys
ENST00000569332.5:c.*928C>G (WWOX)	ENSP00000454788.1:n.*928C>G
ENST00000683929.1:c.*245C>G (WWOX)	ENSP00000507689.1:n.*245C>G
XM_011523100.1:c.1227C>G (WWOX)	XP_011521402.1:p.Asn409Lys
XM_011523103.3:c.*103C>G (WWOX)	XP_011521405.1:n.*103C>G
XM_017023279.1:c.217C>G (WWOX)	XP_016878768.1:p.Gln73Glu
XM_024450279.1:c.*1248G>C (MAF)	XP_024306047.1:n.*1248G>C
XR_001751902.2:n.4450G>C (MAF)
XR_002957802.1:n.4450G>C (MAF)
XR_002957803.1:n.4450G>C (MAF)
XR_002957804.1:n.4450G>C (MAF)