Canonical Allele Identifier: CA396843297

Gene: WWOX

Linked Data

• dbSNP Id: rs370792938
• gnomAD v2: 16-78466519-G-T
• gnomAD v4: 16-78432622-G-T
• COSMIC: COSM3361915 ; COSM3361916
• MyVariant Identifiers: chr16:g.78466519G>T (hg19) ; chr16:g.78432622G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432622G>T , CM000678.2:g.78432622G>T	GRCh38
NC_000016.9:g.78466519G>T , CM000678.1:g.78466519G>T	GRCh37
NC_000016.8:g.77024020G>T	NCBI36
NG_011698.1:g.337969G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.926G>T	ENSP00000485925.2:p.Arg309Leu
ENST00000683929.1:c.926G>T	ENSP00000507689.1:p.Arg309Leu
ENST00000684632.1:n.1305G>T
ENST00000566780.6:c.926G>T MANE Select	ENSP00000457230.1:p.Arg309Leu
ENST00000402655.6:c.409+317468G>T	ENSP00000384238.2:n.409+317468G>T
ENST00000406884.6:c.516+268333G>T	ENSP00000384495.2:n.516+268333G>T
ENST00000408984.7:c.926G>T	ENSP00000386161.3:p.Arg309Leu
ENST00000539474.6:c.409+317468G>T	ENSP00000445210.2:n.409+317468G>T
ENST00000566780.5:c.926G>T	ENSP00000457230.1:p.Arg309Leu
ENST00000569332.5:c.*723G>T	ENSP00000454788.1:n.*723G>T
ENST00000620008.1:c.320G>T	ENSP00000482648.1:p.Arg107Leu
NM_001291997.1:c.587G>T	NP_001278926.1:p.Arg196Leu
NM_016373.3:c.926G>T	NP_057457.1:p.Arg309Leu
XM_006721195.2:c.926G>T	XP_006721258.1:p.Arg309Leu
XM_011523100.1:c.926G>T	XP_011521402.1:p.Arg309Leu
XM_011523101.1:c.926G>T	XP_011521403.1:p.Arg309Leu
XM_011523102.1:c.926G>T	XP_011521404.1:p.Arg309Leu
XM_011523103.1:c.926G>T	XP_011521405.1:p.Arg309Leu
XM_011523104.1:c.926G>T	XP_011521406.1:p.Arg309Leu
XR_933765.1:n.3418+1698C>A
XM_011523101.3:c.926G>T	XP_011521403.1:p.Arg309Leu
XM_011523103.3:c.926G>T	XP_011521405.1:p.Arg309Leu
XM_011523104.3:c.926G>T	XP_011521406.1:p.Arg309Leu
NM_016373.4:c.926G>T MANE Select	NP_057457.1:p.Arg309Leu
NM_001291997.2:c.587G>T	NP_001278926.1:p.Arg196Leu