Canonical Allele Identifier: CA8183758

Gene: WWOX MAF

Linked Data

• ClinVar Variation Id: 235284
• ClinVar RCV Id: RCV000224270 ; RCV000437104 ; RCV001081219 ; RCV002243897 ; RCV002243898
• dbSNP Id: rs200461412
• ExAC: 16:79245589 C / T
• gnomAD v2: 16-79245589-C-T
• gnomAD v3: 16-79211692-C-T
• gnomAD v4: 16-79211692-C-T
• MyVariant Identifiers: chr16:g.79245589C>T (hg19) ; chr16:g.79211692C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211692C>T , CM000678.2:g.79211692C>T	GRCh38
NC_000016.9:g.79245589C>T , CM000678.1:g.79245589C>T	GRCh37
NC_000016.8:g.77803090C>T	NCBI36
NG_011698.1:g.1117039C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*255C>T (WWOX)	ENSP00000507689.1:n.*255C>T
ENST00000566780.6:c.1141C>T (WWOX) MANE Select	ENSP00000457230.1:p.Arg381Cys
ENST00000402655.6:c.494C>T (WWOX)	ENSP00000384238.2:p.Pro165Leu
ENST00000406884.6:c.601C>T (WWOX)	ENSP00000384495.2:p.Arg201Cys
ENST00000539474.6:c.570C>T (WWOX)	ENSP00000445210.2:p.Ala190=
ENST00000566103.1:n.208C>T (WWOX)
ENST00000566780.5:c.1141C>T (WWOX)	ENSP00000457230.1:p.Arg381Cys
ENST00000569332.5:c.*938C>T (WWOX)	ENSP00000454788.1:n.*938C>T
NM_001291997.1:c.802C>T (WWOX)	NP_001278926.1:p.Arg268Cys
NM_016373.3:c.1141C>T (WWOX)	NP_057457.1:p.Arg381Cys
XM_011523100.1:c.1237C>T (WWOX)	XP_011521402.1:p.Arg413Cys
XM_011523103.3:c.*113C>T (WWOX)	XP_011521405.1:n.*113C>T
XM_017023279.1:c.227C>T (WWOX)	XP_016878768.1:p.Pro76Leu
XM_024450279.1:c.*1238G>A (MAF)	XP_024306047.1:n.*1238G>A
XR_001751902.2:n.4440G>A (MAF)
XR_002957802.1:n.4440G>A (MAF)
XR_002957803.1:n.4440G>A (MAF)
XR_002957804.1:n.4440G>A (MAF)
NM_016373.4:c.1141C>T (WWOX) MANE Select	NP_057457.1:p.Arg381Cys
NM_001291997.2:c.802C>T (WWOX)	NP_001278926.1:p.Arg268Cys