Canonical Allele Identifier: CA8183749

Gene: WWOX MAF

Linked Data

• ClinVar Variation Id: 540234
• ClinVar RCV Id: RCV000650203 ; RCV003156275
• dbSNP Id: rs377129275
• ExAC: 16:79245579 C / A
• gnomAD v2: 16-79245579-C-A
• gnomAD v3: 16-79211682-C-A
• gnomAD v4: 16-79211682-C-A
• MyVariant Identifiers: chr16:g.79245579C>A (hg19) ; chr16:g.79211682C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211682C>A , CM000678.2:g.79211682C>A	GRCh38
NC_000016.9:g.79245579C>A , CM000678.1:g.79245579C>A	GRCh37
NC_000016.8:g.77803080C>A	NCBI36
NG_011698.1:g.1117029C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*245C>A (WWOX)	ENSP00000507689.1:n.*245C>A
ENST00000566780.6:c.1131C>A (WWOX) MANE Select	ENSP00000457230.1:p.Asn377Lys
ENST00000402655.6:c.484C>A (WWOX)	ENSP00000384238.2:p.Gln162Lys
ENST00000406884.6:c.591C>A (WWOX)	ENSP00000384495.2:p.Asn197Lys
ENST00000539474.6:c.560C>A (WWOX)	ENSP00000445210.2:p.Thr187Lys
ENST00000566103.1:n.198C>A (WWOX)
ENST00000566780.5:c.1131C>A (WWOX)	ENSP00000457230.1:p.Asn377Lys
ENST00000569332.5:c.*928C>A (WWOX)	ENSP00000454788.1:n.*928C>A
NM_001291997.1:c.792C>A (WWOX)	NP_001278926.1:p.Asn264Lys
NM_016373.3:c.1131C>A (WWOX)	NP_057457.1:p.Asn377Lys
XM_011523100.1:c.1227C>A (WWOX)	XP_011521402.1:p.Asn409Lys
XM_011523103.3:c.*103C>A (WWOX)	XP_011521405.1:n.*103C>A
XM_017023279.1:c.217C>A (WWOX)	XP_016878768.1:p.Gln73Lys
XM_024450279.1:c.*1248G>T (MAF)	XP_024306047.1:n.*1248G>T
XR_001751902.2:n.4450G>T (MAF)
XR_002957802.1:n.4450G>T (MAF)
XR_002957803.1:n.4450G>T (MAF)
XR_002957804.1:n.4450G>T (MAF)
NM_016373.4:c.1131C>A (WWOX) MANE Select	NP_057457.1:p.Asn377Lys
NM_001291997.2:c.792C>A (WWOX)	NP_001278926.1:p.Asn264Lys