Canonical Allele Identifier: CA2234946427

Gene: WWOX

Linked Data

• dbSNP Id: rs1597372094

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78224819T>A , CM000678.2:g.78224819T>A	GRCh38
NC_000016.9:g.78258716T>A , CM000678.1:g.78258716T>A	GRCh37
NC_000016.8:g.76816217T>A	NCBI36
NG_011698.1:g.130166T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.516+60530T>A	ENSP00000485925.2:n.516+60530T>A
ENST00000683286.1:n.843+60530T>A
ENST00000683929.1:c.516+60530T>A	ENSP00000507689.1:n.516+60530T>A
ENST00000684070.1:n.780+60530T>A
ENST00000684632.1:n.895+60530T>A
ENST00000566780.6:c.516+60530T>A MANE Select	ENSP00000457230.1:n.516+60530T>A
ENST00000355860.7:c.517-53784T>A	ENSP00000348119.3:n.517-53784T>A
ENST00000402655.6:c.409+109665T>A	ENSP00000384238.2:n.409+109665T>A
ENST00000406884.6:c.516+60530T>A	ENSP00000384495.2:n.516+60530T>A
ENST00000408984.7:c.516+60530T>A	ENSP00000386161.3:n.516+60530T>A
ENST00000539474.6:c.409+109665T>A	ENSP00000445210.2:n.409+109665T>A
ENST00000561846.5:n.561-56022T>A
ENST00000562639.5:n.204+60530T>A
ENST00000563358.5:n.624-53784T>A
ENST00000565791.1:n.204-39650T>A
ENST00000566662.5:c.*134+60530T>A	ENSP00000454331.1:n.*134+60530T>A
ENST00000566780.5:c.516+60530T>A	ENSP00000457230.1:n.516+60530T>A
ENST00000569332.5:c.*313+60530T>A	ENSP00000454788.1:n.*313+60530T>A
ENST00000627394.2:c.*314-53784T>A	ENSP00000485925.1:n.*314-53784T>A
NM_001291997.1:c.177+60530T>A	NP_001278926.1:n.177+60530T>A
NM_016373.3:c.516+60530T>A	NP_057457.1:n.516+60530T>A
NM_130791.3:c.517-53784T>A	NP_570607.1:n.517-53784T>A
NR_120436.1:n.997-53784T>A
XM_006721195.2:c.516+60530T>A	XP_006721258.1:n.516+60530T>A
XM_011523100.1:c.516+60530T>A	XP_011521402.1:n.516+60530T>A
XM_011523101.1:c.516+60530T>A	XP_011521403.1:n.516+60530T>A
XM_011523102.1:c.516+60530T>A	XP_011521404.1:n.516+60530T>A
XM_011523103.1:c.516+60530T>A	XP_011521405.1:n.516+60530T>A
XM_011523104.1:c.516+60530T>A	XP_011521406.1:n.516+60530T>A
XM_011523105.1:c.517-3961T>A	XP_011521407.1:n.517-3961T>A
XM_011523101.3:c.516+60530T>A	XP_011521403.1:n.516+60530T>A
XM_011523103.3:c.516+60530T>A	XP_011521405.1:n.516+60530T>A
XM_011523104.3:c.516+60530T>A	XP_011521406.1:n.516+60530T>A
XM_011523105.3:c.517-3961T>A	XP_011521407.1:n.517-3961T>A
XM_017023278.2:c.516+60530T>A	XP_016878767.1:n.516+60530T>A
NM_016373.4:c.516+60530T>A MANE Select	NP_057457.1:n.516+60530T>A
NM_001291997.2:c.177+60530T>A	NP_001278926.1:n.177+60530T>A
NM_130791.4:c.517-53784T>A	NP_570607.1:n.517-53784T>A
NR_120436.2:n.756-53784T>A
NM_130791.5:c.517-53784T>A	NP_570607.1:n.517-53784T>A
NR_120436.3:n.756-53784T>A