Canonical Allele Identifier: CA396537100

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211677T>C , CM000678.2:g.79211677T>C	GRCh38
NC_000016.9:g.79245574T>C , CM000678.1:g.79245574T>C	GRCh37
NC_000016.8:g.77803075T>C	NCBI36
NG_011698.1:g.1117024T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1126T>C (WWOX) MANE Select	NP_057457.1:p.Phe376Leu
ENST00000566780.6:c.1126T>C (WWOX) MANE Select	ENSP00000457230.1:p.Phe376Leu
NM_001291997.1:c.787T>C (WWOX)	NP_001278926.1:p.Phe263Leu
NM_001291997.2:c.787T>C (WWOX)	NP_001278926.1:p.Phe263Leu
NM_016373.3:c.1126T>C (WWOX)	NP_057457.1:p.Phe376Leu
ENST00000402655.6:c.479T>C (WWOX)	ENSP00000384238.2:p.Leu160Pro
ENST00000406884.6:c.586T>C (WWOX)	ENSP00000384495.2:p.Phe196Leu
ENST00000539474.6:c.555T>C (WWOX)	ENSP00000445210.2:p.Thr185=
ENST00000566103.1:n.193T>C (WWOX)
ENST00000566780.5:c.1126T>C (WWOX)	ENSP00000457230.1:p.Phe376Leu
ENST00000569332.5:c.*923T>C (WWOX)	ENSP00000454788.1:n.*923T>C
ENST00000683929.1:c.*240T>C (WWOX)	ENSP00000507689.1:n.*240T>C
XM_011523100.1:c.1222T>C (WWOX)	XP_011521402.1:p.Phe408Leu
XM_011523103.3:c.*98T>C (WWOX)	XP_011521405.1:n.*98T>C
XM_017023279.1:c.212T>C (WWOX)	XP_016878768.1:p.Leu71Pro
XM_024450279.1:c.*1253A>G (MAF)	XP_024306047.1:n.*1253A>G
XR_001751902.2:n.4455A>G (MAF)
XR_002957802.1:n.4455A>G (MAF)
XR_002957803.1:n.4455A>G (MAF)
XR_002957804.1:n.4455A>G (MAF)