Canonical Allele Identifier: CA396843091

Gene: WWOX

Linked Data

• ClinVar Variation Id: 2300568
• ClinVar RCV Id: RCV002850360
• MyVariant Identifiers: chr16:g.78466416C>A (hg19) ; chr16:g.78432519C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432519C>A , CM000678.2:g.78432519C>A	GRCh38
NC_000016.9:g.78466416C>A , CM000678.1:g.78466416C>A	GRCh37
NC_000016.8:g.77023917C>A	NCBI36
NG_011698.1:g.337866C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.823C>A	ENSP00000485925.2:p.Leu275Met
ENST00000683929.1:c.823C>A	ENSP00000507689.1:p.Leu275Met
ENST00000684632.1:n.1202C>A
ENST00000566780.6:c.823C>A MANE Select	ENSP00000457230.1:p.Leu275Met
ENST00000402655.6:c.409+317365C>A	ENSP00000384238.2:n.409+317365C>A
ENST00000406884.6:c.516+268230C>A	ENSP00000384495.2:n.516+268230C>A
ENST00000408984.7:c.823C>A	ENSP00000386161.3:p.Leu275Met
ENST00000539474.6:c.409+317365C>A	ENSP00000445210.2:n.409+317365C>A
ENST00000562639.5:n.511C>A
ENST00000566780.5:c.823C>A	ENSP00000457230.1:p.Leu275Met
ENST00000569332.5:c.*620C>A	ENSP00000454788.1:n.*620C>A
ENST00000620008.1:c.217C>A	ENSP00000482648.1:p.Leu73Met
NM_001291997.1:c.484C>A	NP_001278926.1:p.Leu162Met
NM_016373.3:c.823C>A	NP_057457.1:p.Leu275Met
XM_006721195.2:c.823C>A	XP_006721258.1:p.Leu275Met
XM_011523100.1:c.823C>A	XP_011521402.1:p.Leu275Met
XM_011523101.1:c.823C>A	XP_011521403.1:p.Leu275Met
XM_011523102.1:c.823C>A	XP_011521404.1:p.Leu275Met
XM_011523103.1:c.823C>A	XP_011521405.1:p.Leu275Met
XM_011523104.1:c.823C>A	XP_011521406.1:p.Leu275Met
XR_933765.1:n.3419-1706G>T
XM_011523101.3:c.823C>A	XP_011521403.1:p.Leu275Met
XM_011523103.3:c.823C>A	XP_011521405.1:p.Leu275Met
XM_011523104.3:c.823C>A	XP_011521406.1:p.Leu275Met
NM_016373.4:c.823C>A MANE Select	NP_057457.1:p.Leu275Met
NM_001291997.2:c.484C>A	NP_001278926.1:p.Leu162Met