Canonical Allele Identifier: CA8183814

Gene: WWOX MAF

Linked Data

• ClinVar Variation Id: 382759
• ClinVar RCV Id: RCV000422776 ; RCV000714203 ; RCV002244891 ; RCV002244892
• dbSNP Id: rs140060332
• ExAC: 16:79245696 G / T
• gnomAD v2: 16-79245696-G-T
• gnomAD v3: 16-79211799-G-T
• gnomAD v4: 16-79211799-G-T
• MyVariant Identifiers: chr16:g.79245696G>T (hg19) ; chr16:g.79211799G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211799G>T , CM000678.2:g.79211799G>T	GRCh38
NC_000016.9:g.79245696G>T , CM000678.1:g.79245696G>T	GRCh37
NC_000016.8:g.77803197G>T	NCBI36
NG_011698.1:g.1117146G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*362G>T (WWOX)	ENSP00000507689.1:n.*362G>T
ENST00000566780.6:c.*3G>T (WWOX) MANE Select	ENSP00000457230.1:n.*3G>T
ENST00000402655.6:c.601G>T (WWOX)	ENSP00000384238.2:p.Gly201Ter
ENST00000406884.6:c.*3G>T (WWOX)	ENSP00000384495.2:n.*3G>T
ENST00000539474.6:c.*35G>T (WWOX)	ENSP00000445210.2:n.*35G>T
ENST00000566103.1:n.315G>T (WWOX)
ENST00000566780.5:c.*3G>T (WWOX)	ENSP00000457230.1:n.*3G>T
ENST00000569332.5:c.*1045G>T (WWOX)	ENSP00000454788.1:n.*1045G>T
NM_001291997.1:c.*3G>T (WWOX)	NP_001278926.1:n.*3G>T
NM_016373.3:c.*3G>T (WWOX)	NP_057457.1:n.*3G>T
XM_011523100.1:c.*3G>T (WWOX)	XP_011521402.1:n.*3G>T
XM_011523103.3:c.*220G>T (WWOX)	XP_011521405.1:n.*220G>T
XM_017023279.1:c.334G>T (WWOX)	XP_016878768.1:p.Gly112Ter
XM_024450279.1:c.*1131C>A (MAF)	XP_024306047.1:n.*1131C>A
XR_001751902.2:n.4333C>A (MAF)
XR_002957802.1:n.4333C>A (MAF)
XR_002957803.1:n.4333C>A (MAF)
XR_002957804.1:n.4333C>A (MAF)
NM_016373.4:c.*3G>T (WWOX) MANE Select	NP_057457.1:n.*3G>T
NM_001291997.2:c.*3G>T (WWOX)	NP_001278926.1:n.*3G>T