Canonical Allele Identifier: CA8183715

Gene: WWOX MAF

Linked Data

• ClinVar Variation Id: 260736
• ClinVar RCV Id: RCV000247690 ; RCV001515358 ; RCV002244634 ; RCV002244635
• dbSNP Id: rs66481974
• ExAC: 16:79245491 T / C
• gnomAD v2: 16-79245491-T-C
• gnomAD v3: 16-79211594-T-C
• gnomAD v4: 16-79211594-T-C
• MyVariant Identifiers: chr16:g.79245491T>C (hg19) ; chr16:g.79211594T>C (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211594T>C , CM000678.2:g.79211594T>C	GRCh38
NC_000016.9:g.79245491T>C , CM000678.1:g.79245491T>C	GRCh37
NC_000016.8:g.77802992T>C	NCBI36
NG_011698.1:g.1116941T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*171-14T>C (WWOX)	ENSP00000507689.1:n.*171-14T>C
ENST00000566780.6:c.1057-14T>C (WWOX) MANE Select	ENSP00000457230.1:n.1057-14T>C
ENST00000402655.6:c.410-14T>C (WWOX)	ENSP00000384238.2:n.410-14T>C
ENST00000406884.6:c.517-14T>C (WWOX)	ENSP00000384495.2:n.517-14T>C
ENST00000539474.6:c.486-14T>C (WWOX)	ENSP00000445210.2:n.486-14T>C
ENST00000566103.1:n.124-14T>C (WWOX)
ENST00000566780.5:c.1057-14T>C (WWOX)	ENSP00000457230.1:n.1057-14T>C
ENST00000569332.5:c.*854-14T>C (WWOX)	ENSP00000454788.1:n.*854-14T>C
NM_001291997.1:c.718-14T>C (WWOX)	NP_001278926.1:n.718-14T>C
NM_016373.3:c.1057-14T>C (WWOX)	NP_057457.1:n.1057-14T>C
XM_011523100.1:c.1153-14T>C (WWOX)	XP_011521402.1:n.1153-14T>C
XM_011523103.1:c.*29-14T>C (WWOX)	XP_011521405.1:n.*29-14T>C
XR_933762.1:n.7A>G
XM_011523103.3:c.*29-14T>C (WWOX)	XP_011521405.1:n.*29-14T>C
XM_017023279.1:c.143-14T>C (WWOX)	XP_016878768.1:n.143-14T>C
XM_024450279.1:c.*1336A>G (MAF)	XP_024306047.1:n.*1336A>G
XR_001751902.2:n.4538A>G (MAF)
XR_002957802.1:n.4538A>G (MAF)
XR_002957803.1:n.4538A>G (MAF)
XR_002957804.1:n.4538A>G (MAF)
NM_016373.4:c.1057-14T>C (WWOX) MANE Select	NP_057457.1:n.1057-14T>C
NM_001291997.2:c.718-14T>C (WWOX)	NP_001278926.1:n.718-14T>C