Canonical Allele Identifier: CA396537233

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211736G>C , CM000678.2:g.79211736G>C	GRCh38
NC_000016.9:g.79245633G>C , CM000678.1:g.79245633G>C	GRCh37
NC_000016.8:g.77803134G>C	NCBI36
NG_011698.1:g.1117083G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*299G>C (WWOX)	ENSP00000507689.1:n.*299G>C
ENST00000566780.6:c.1185G>C (WWOX) MANE Select	ENSP00000457230.1:p.Arg395=
ENST00000402655.6:c.538G>C (WWOX)	ENSP00000384238.2:p.Asp180His
ENST00000406884.6:c.645G>C (WWOX)	ENSP00000384495.2:p.Arg215=
ENST00000539474.6:c.614G>C (WWOX)	ENSP00000445210.2:p.Gly205Ala
ENST00000566103.1:n.252G>C (WWOX)
ENST00000566780.5:c.1185G>C (WWOX)	ENSP00000457230.1:p.Arg395=
ENST00000569332.5:c.*982G>C (WWOX)	ENSP00000454788.1:n.*982G>C
NM_001291997.1:c.846G>C (WWOX)	NP_001278926.1:p.Arg282=
NM_016373.3:c.1185G>C (WWOX)	NP_057457.1:p.Arg395=
XM_011523100.1:c.1281G>C (WWOX)	XP_011521402.1:p.Arg427=
XM_011523103.3:c.*157G>C (WWOX)	XP_011521405.1:n.*157G>C
XM_017023279.1:c.271G>C (WWOX)	XP_016878768.1:p.Asp91His
XM_024450279.1:c.*1194C>G (MAF)	XP_024306047.1:n.*1194C>G
XR_001751902.2:n.4396C>G (MAF)
XR_002957802.1:n.4396C>G (MAF)
XR_002957803.1:n.4396C>G (MAF)
XR_002957804.1:n.4396C>G (MAF)
NM_016373.4:c.1185G>C (WWOX) MANE Select	NP_057457.1:p.Arg395=
NM_001291997.2:c.846G>C (WWOX)	NP_001278926.1:p.Arg282=