Canonical Allele Identifier: CA8183813

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211797G>C , CM000678.2:g.79211797G>C	GRCh38
NC_000016.9:g.79245694G>C , CM000678.1:g.79245694G>C	GRCh37
NC_000016.8:g.77803195G>C	NCBI36
NG_011698.1:g.1117144G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*360G>C (WWOX)	ENSP00000507689.1:n.*360G>C
ENST00000566780.6:c.*1G>C (WWOX) MANE Select	ENSP00000457230.1:n.*1G>C
ENST00000402655.6:c.599G>C (WWOX)	ENSP00000384238.2:p.Ser200Thr
ENST00000406884.6:c.*1G>C (WWOX)	ENSP00000384495.2:n.*1G>C
ENST00000539474.6:c.*33G>C (WWOX)	ENSP00000445210.2:n.*33G>C
ENST00000566103.1:n.313G>C (WWOX)
ENST00000566780.5:c.*1G>C (WWOX)	ENSP00000457230.1:n.*1G>C
ENST00000569332.5:c.*1043G>C (WWOX)	ENSP00000454788.1:n.*1043G>C
NM_001291997.1:c.*1G>C (WWOX)	NP_001278926.1:n.*1G>C
NM_016373.3:c.*1G>C (WWOX)	NP_057457.1:n.*1G>C
XM_011523100.1:c.*1G>C (WWOX)	XP_011521402.1:n.*1G>C
XM_011523103.3:c.*218G>C (WWOX)	XP_011521405.1:n.*218G>C
XM_017023279.1:c.332G>C (WWOX)	XP_016878768.1:p.Ser111Thr
XM_024450279.1:c.*1133C>G (MAF)	XP_024306047.1:n.*1133C>G
XR_001751902.2:n.4335C>G (MAF)
XR_002957802.1:n.4335C>G (MAF)
XR_002957803.1:n.4335C>G (MAF)
XR_002957804.1:n.4335C>G (MAF)
NM_016373.4:c.*1G>C (WWOX) MANE Select	NP_057457.1:n.*1G>C
NM_001291997.2:c.*1G>C (WWOX)	NP_001278926.1:n.*1G>C