Canonical Allele Identifier: CA8183863

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211889A>G , CM000678.2:g.79211889A>G	GRCh38
NC_000016.9:g.79245786A>G , CM000678.1:g.79245786A>G	GRCh37
NC_000016.8:g.77803287A>G	NCBI36
NG_011698.1:g.1117236A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.*93A>G (WWOX) MANE Select	NP_057457.1:n.*93A>G
ENST00000566780.6:c.*93A>G (WWOX) MANE Select	ENSP00000457230.1:n.*93A>G
NM_001291997.1:c.*93A>G (WWOX)	NP_001278926.1:n.*93A>G
NM_001291997.2:c.*93A>G (WWOX)	NP_001278926.1:n.*93A>G
NM_016373.3:c.*93A>G (WWOX)	NP_057457.1:n.*93A>G
ENST00000402655.6:c.691A>G (WWOX)	ENSP00000384238.2:p.Thr231Ala
ENST00000406884.6:c.*93A>G (WWOX)	ENSP00000384495.2:n.*93A>G
ENST00000539474.6:c.*125A>G (WWOX)	ENSP00000445210.2:n.*125A>G
ENST00000566103.1:n.405A>G (WWOX)
ENST00000566780.5:c.*93A>G (WWOX)	ENSP00000457230.1:n.*93A>G
ENST00000569332.5:c.*1135A>G (WWOX)	ENSP00000454788.1:n.*1135A>G
ENST00000683929.1:c.*452A>G (WWOX)	ENSP00000507689.1:n.*452A>G
XM_011523100.1:c.*93A>G (WWOX)	XP_011521402.1:n.*93A>G
XM_011523103.3:c.*310A>G (WWOX)	XP_011521405.1:n.*310A>G
XM_017023279.1:c.424A>G (WWOX)	XP_016878768.1:p.Thr142Ala
XM_024450279.1:c.*1041T>C (MAF)	XP_024306047.1:n.*1041T>C
XR_001751902.2:n.4243T>C (MAF)
XR_002957802.1:n.4243T>C (MAF)
XR_002957803.1:n.4243T>C (MAF)
XR_002957804.1:n.4243T>C (MAF)