Canonical Allele Identifier: CA396537602

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211923G>A , CM000678.2:g.79211923G>A	GRCh38
NC_000016.9:g.79245820G>A , CM000678.1:g.79245820G>A	GRCh37
NC_000016.8:g.77803321G>A	NCBI36
NG_011698.1:g.1117270G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.*127G>A (WWOX) MANE Select	NP_057457.1:n.*127G>A
ENST00000566780.6:c.*127G>A (WWOX) MANE Select	ENSP00000457230.1:n.*127G>A
NM_001291997.1:c.*127G>A (WWOX)	NP_001278926.1:n.*127G>A
NM_001291997.2:c.*127G>A (WWOX)	NP_001278926.1:n.*127G>A
NM_016373.3:c.*127G>A (WWOX)	NP_057457.1:n.*127G>A
ENST00000402655.6:c.725G>A (WWOX)	ENSP00000384238.2:p.Ser242Asn
ENST00000406884.6:c.*127G>A (WWOX)	ENSP00000384495.2:n.*127G>A
ENST00000539474.6:c.*159G>A (WWOX)	ENSP00000445210.2:n.*159G>A
ENST00000566103.1:n.439G>A (WWOX)
ENST00000566780.5:c.*127G>A (WWOX)	ENSP00000457230.1:n.*127G>A
ENST00000569332.5:c.*1169G>A (WWOX)	ENSP00000454788.1:n.*1169G>A
ENST00000683929.1:c.*486G>A (WWOX)	ENSP00000507689.1:n.*486G>A
XM_011523100.1:c.*127G>A (WWOX)	XP_011521402.1:n.*127G>A
XM_011523103.3:c.*344G>A (WWOX)	XP_011521405.1:n.*344G>A
XM_017023279.1:c.458G>A (WWOX)	XP_016878768.1:p.Ser153Asn
XM_024450279.1:c.*1007C>T (MAF)	XP_024306047.1:n.*1007C>T
XR_001751902.2:n.4209C>T (MAF)
XR_002957802.1:n.4209C>T (MAF)
XR_002957803.1:n.4209C>T (MAF)
XR_002957804.1:n.4209C>T (MAF)