Canonical Allele Identifier: CA396843077

Gene: WWOX

Linked Data

• dbSNP Id: rs186745328
• gnomAD v3: 16-78432512-G-C
• gnomAD v4: 16-78432512-G-C
• MyVariant Identifiers: chr16:g.78466409G>C (hg19) ; chr16:g.78432512G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432512G>C , CM000678.2:g.78432512G>C	GRCh38
NC_000016.9:g.78466409G>C , CM000678.1:g.78466409G>C	GRCh37
NC_000016.8:g.77023910G>C	NCBI36
NG_011698.1:g.337859G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.816G>C	ENSP00000485925.2:p.Leu272Phe
ENST00000683929.1:c.816G>C	ENSP00000507689.1:p.Leu272Phe
ENST00000684632.1:n.1195G>C
ENST00000566780.6:c.816G>C MANE Select	ENSP00000457230.1:p.Leu272Phe
ENST00000402655.6:c.409+317358G>C	ENSP00000384238.2:n.409+317358G>C
ENST00000406884.6:c.516+268223G>C	ENSP00000384495.2:n.516+268223G>C
ENST00000408984.7:c.816G>C	ENSP00000386161.3:p.Leu272Phe
ENST00000539474.6:c.409+317358G>C	ENSP00000445210.2:n.409+317358G>C
ENST00000562639.5:n.504G>C
ENST00000566780.5:c.816G>C	ENSP00000457230.1:p.Leu272Phe
ENST00000569332.5:c.*613G>C	ENSP00000454788.1:n.*613G>C
ENST00000620008.1:c.210G>C	ENSP00000482648.1:p.Leu70Phe
NM_001291997.1:c.477G>C	NP_001278926.1:p.Leu159Phe
NM_016373.3:c.816G>C	NP_057457.1:p.Leu272Phe
XM_006721195.2:c.816G>C	XP_006721258.1:p.Leu272Phe
XM_011523100.1:c.816G>C	XP_011521402.1:p.Leu272Phe
XM_011523101.1:c.816G>C	XP_011521403.1:p.Leu272Phe
XM_011523102.1:c.816G>C	XP_011521404.1:p.Leu272Phe
XM_011523103.1:c.816G>C	XP_011521405.1:p.Leu272Phe
XM_011523104.1:c.816G>C	XP_011521406.1:p.Leu272Phe
XR_933765.1:n.3419-1699C>G
XM_011523101.3:c.816G>C	XP_011521403.1:p.Leu272Phe
XM_011523103.3:c.816G>C	XP_011521405.1:p.Leu272Phe
XM_011523104.3:c.816G>C	XP_011521406.1:p.Leu272Phe
NM_016373.4:c.816G>C MANE Select	NP_057457.1:p.Leu272Phe
NM_001291997.2:c.477G>C	NP_001278926.1:p.Leu159Phe