Canonical Allele Identifier: CA249927

Gene: WWOX

Linked Data

• ClinVar Variation Id: 183303
• ClinVar RCV Id: RCV000162124 ; RCV000408849 ; RCV001220865 ; RCV001558644 ; RCV003398828
• dbSNP Id: rs730882215
• gnomAD v2: 16-78458766-G-A
• gnomAD v4: 16-78424869-G-A
• MyVariant Identifiers: chr16:g.78458766G>A (hg19) ; chr16:g.78424869G>A (hg38)
• PubMed: PMID:25558065

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78424869G>A , CM000678.2:g.78424869G>A	GRCh38
NC_000016.9:g.78458766G>A , CM000678.1:g.78458766G>A	GRCh37
NC_000016.8:g.77016267G>A	NCBI36
NG_011698.1:g.330216G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.606-1G>A	ENSP00000485925.2:n.606-1G>A
ENST00000683929.1:c.606-1G>A	ENSP00000507689.1:n.606-1G>A
ENST00000684632.1:n.985-1G>A
ENST00000566780.6:c.606-1G>A MANE Select	ENSP00000457230.1:n.606-1G>A
ENST00000402655.6:c.409+309715G>A	ENSP00000384238.2:n.409+309715G>A
ENST00000406884.6:c.516+260580G>A	ENSP00000384495.2:n.516+260580G>A
ENST00000408984.7:c.606-1G>A	ENSP00000386161.3:n.606-1G>A
ENST00000539474.6:c.409+309715G>A	ENSP00000445210.2:n.409+309715G>A
ENST00000562639.5:n.294-1G>A
ENST00000566662.5:c.*224-1G>A	ENSP00000454331.1:n.*224-1G>A
ENST00000566780.5:c.606-1G>A	ENSP00000457230.1:n.606-1G>A
ENST00000569332.5:c.*403-1G>A	ENSP00000454788.1:n.*403-1G>A
NM_001291997.1:c.267-1G>A	NP_001278926.1:n.267-1G>A
NM_016373.3:c.606-1G>A	NP_057457.1:n.606-1G>A
XM_006721195.2:c.606-1G>A	XP_006721258.1:n.606-1G>A
XM_011523100.1:c.606-1G>A	XP_011521402.1:n.606-1G>A
XM_011523101.1:c.606-1G>A	XP_011521403.1:n.606-1G>A
XM_011523102.1:c.606-1G>A	XP_011521404.1:n.606-1G>A
XM_011523103.1:c.606-1G>A	XP_011521405.1:n.606-1G>A
XM_011523104.1:c.606-1G>A	XP_011521406.1:n.606-1G>A
XR_933765.1:n.3806+5557C>T
XM_011523101.3:c.606-1G>A	XP_011521403.1:n.606-1G>A
XM_011523103.3:c.606-1G>A	XP_011521405.1:n.606-1G>A
XM_011523104.3:c.606-1G>A	XP_011521406.1:n.606-1G>A
NM_016373.4:c.606-1G>A MANE Select	NP_057457.1:n.606-1G>A
NM_001291997.2:c.267-1G>A	NP_001278926.1:n.267-1G>A