Canonical Allele Identifier: CA396843099

Gene: WWOX

Linked Data

• ClinVar Variation Id: 1450730
• ClinVar RCV Id: RCV002014842
• dbSNP Id: rs2083246915
• gnomAD v4: 16-78432523-A-C
• MyVariant Identifiers: chr16:g.78466420A>C (hg19) ; chr16:g.78432523A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432523A>C , CM000678.2:g.78432523A>C	GRCh38
NC_000016.9:g.78466420A>C , CM000678.1:g.78466420A>C	GRCh37
NC_000016.8:g.77023921A>C	NCBI36
NG_011698.1:g.337870A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.827A>C	ENSP00000485925.2:p.Asp276Ala
ENST00000683929.1:c.827A>C	ENSP00000507689.1:p.Asp276Ala
ENST00000684632.1:n.1206A>C
ENST00000566780.6:c.827A>C MANE Select	ENSP00000457230.1:p.Asp276Ala
ENST00000402655.6:c.409+317369A>C	ENSP00000384238.2:n.409+317369A>C
ENST00000406884.6:c.516+268234A>C	ENSP00000384495.2:n.516+268234A>C
ENST00000408984.7:c.827A>C	ENSP00000386161.3:p.Asp276Ala
ENST00000539474.6:c.409+317369A>C	ENSP00000445210.2:n.409+317369A>C
ENST00000562639.5:n.515A>C
ENST00000566780.5:c.827A>C	ENSP00000457230.1:p.Asp276Ala
ENST00000569332.5:c.*624A>C	ENSP00000454788.1:n.*624A>C
ENST00000620008.1:c.221A>C	ENSP00000482648.1:p.Asp74Ala
NM_001291997.1:c.488A>C	NP_001278926.1:p.Asp163Ala
NM_016373.3:c.827A>C	NP_057457.1:p.Asp276Ala
XM_006721195.2:c.827A>C	XP_006721258.1:p.Asp276Ala
XM_011523100.1:c.827A>C	XP_011521402.1:p.Asp276Ala
XM_011523101.1:c.827A>C	XP_011521403.1:p.Asp276Ala
XM_011523102.1:c.827A>C	XP_011521404.1:p.Asp276Ala
XM_011523103.1:c.827A>C	XP_011521405.1:p.Asp276Ala
XM_011523104.1:c.827A>C	XP_011521406.1:p.Asp276Ala
XR_933765.1:n.3419-1710T>G
XM_011523101.3:c.827A>C	XP_011521403.1:p.Asp276Ala
XM_011523103.3:c.827A>C	XP_011521405.1:p.Asp276Ala
XM_011523104.3:c.827A>C	XP_011521406.1:p.Asp276Ala
NM_016373.4:c.827A>C MANE Select	NP_057457.1:p.Asp276Ala
NM_001291997.2:c.488A>C	NP_001278926.1:p.Asp163Ala