Canonical Allele Identifier: CA16043515

Gene: WWOX

Linked Data

• ClinVar Variation Id: 373950
• ClinVar RCV Id: RCV000415161
• dbSNP Id: rs1057518795
• gnomAD v2: 16-78466510-AG-A
• gnomAD v4: 16-78432613-AG-A
• MyVariant Identifiers: chr16:g.78466511del (hg19) ; chr16:g.78432614del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432614del , CM000678.2:g.78432614del	GRCh38
NC_000016.9:g.78466511del , CM000678.1:g.78466511del	GRCh37
NC_000016.8:g.77024012del	NCBI36
NG_011698.1:g.337961del

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.918del	ENSP00000485925.2:p.Glu306AspfsTer21
ENST00000683929.1:c.918del	ENSP00000507689.1:p.Glu306AspfsTer21
ENST00000684632.1:n.1297del
ENST00000566780.6:c.918del MANE Select	ENSP00000457230.1:p.Glu306AspfsTer21
ENST00000402655.6:c.409+317460del	ENSP00000384238.2:n.409+317460del
ENST00000406884.6:c.516+268325del	ENSP00000384495.2:n.516+268325del
ENST00000408984.7:c.918del	ENSP00000386161.3:p.Glu306AspfsTer21
ENST00000539474.6:c.409+317460del	ENSP00000445210.2:n.409+317460del
ENST00000566780.5:c.918del	ENSP00000457230.1:p.Glu306AspfsTer21
ENST00000569332.5:c.*715del	ENSP00000454788.1:n.*715del
ENST00000620008.1:c.312del	ENSP00000482648.1:p.Glu104AspfsTer21
NM_001291997.1:c.579del	NP_001278926.1:p.Glu193AspfsTer21
NM_016373.3:c.918del	NP_057457.1:p.Glu306AspfsTer21
XM_006721195.2:c.918del	XP_006721258.1:p.Glu306AspfsTer21
XM_011523100.1:c.918del	XP_011521402.1:p.Glu306AspfsTer21
XM_011523101.1:c.918del	XP_011521403.1:p.Glu306AspfsTer21
XM_011523102.1:c.918del	XP_011521404.1:p.Glu306AspfsTer21
XM_011523103.1:c.918del	XP_011521405.1:p.Glu306AspfsTer21
XM_011523104.1:c.918del	XP_011521406.1:p.Glu306AspfsTer21
XR_933765.1:n.3418+1706del
XM_011523101.3:c.918del	XP_011521403.1:p.Glu306AspfsTer21
XM_011523103.3:c.918del	XP_011521405.1:p.Glu306AspfsTer21
XM_011523104.3:c.918del	XP_011521406.1:p.Glu306AspfsTer21
NM_016373.4:c.918del MANE Select	NP_057457.1:p.Glu306AspfsTer21
NM_001291997.2:c.579del	NP_001278926.1:p.Glu193AspfsTer21