Canonical Allele Identifier: CA2234905900

Gene: WWOX

Linked Data

• dbSNP Id: rs2034547303

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78154932_78154941del , CM000678.2:g.78154932_78154941del	GRCh38
NC_000016.9:g.78188829_78188838del , CM000678.1:g.78188829_78188838del	GRCh37
NC_000016.8:g.76746330_76746339del	NCBI36
NG_011698.1:g.60279_60288del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.410-9251_410-9242del	ENSP00000485925.2:n.410-9251_410-9242del
ENST00000683286.1:n.737-9251_737-9242del
ENST00000683929.1:c.410-9251_410-9242del	ENSP00000507689.1:n.410-9251_410-9242del
ENST00000684070.1:n.674-9251_674-9242del
ENST00000684632.1:n.789-9251_789-9242del
ENST00000566780.6:c.410-9251_410-9242del MANE Select	ENSP00000457230.1:n.410-9251_410-9242del
ENST00000355860.7:c.410-9251_410-9242del	ENSP00000348119.3:n.410-9251_410-9242del
ENST00000402655.6:c.409+39778_409+39787del	ENSP00000384238.2:n.409+39778_409+39787del
ENST00000406884.6:c.410-9251_410-9242del	ENSP00000384495.2:n.410-9251_410-9242del
ENST00000408984.7:c.410-9251_410-9242del	ENSP00000386161.3:n.410-9251_410-9242del
ENST00000539474.6:c.409+39778_409+39787del	ENSP00000445210.2:n.409+39778_409+39787del
ENST00000561846.5:n.454-9251_454-9242del
ENST00000562639.5:n.98-9251_98-9242del
ENST00000563358.5:n.517-9251_517-9242del
ENST00000565791.1:n.17+8999_17+9008del
ENST00000566662.5:c.*28-9251_*28-9242del	ENSP00000454331.1:n.*28-9251_*28-9242del
ENST00000566780.5:c.410-9251_410-9242del	ENSP00000457230.1:n.410-9251_410-9242del
ENST00000569332.5:c.*207-9251_*207-9242del	ENSP00000454788.1:n.*207-9251_*207-9242del
ENST00000627394.2:c.*207-9251_*207-9242del	ENSP00000485925.1:n.*207-9251_*207-9242del
NM_001291997.1:c.71-9251_71-9242del	NP_001278926.1:n.71-9251_71-9242del
NM_016373.3:c.410-9251_410-9242del	NP_057457.1:n.410-9251_410-9242del
NM_130791.3:c.410-9251_410-9242del	NP_570607.1:n.410-9251_410-9242del
NR_120436.1:n.890-9251_890-9242del
XM_006721195.2:c.410-9251_410-9242del	XP_006721258.1:n.410-9251_410-9242del
XM_011523100.1:c.410-9251_410-9242del	XP_011521402.1:n.410-9251_410-9242del
XM_011523101.1:c.410-9251_410-9242del	XP_011521403.1:n.410-9251_410-9242del
XM_011523102.1:c.410-9251_410-9242del	XP_011521404.1:n.410-9251_410-9242del
XM_011523103.1:c.410-9251_410-9242del	XP_011521405.1:n.410-9251_410-9242del
XM_011523104.1:c.410-9251_410-9242del	XP_011521406.1:n.410-9251_410-9242del
XM_011523105.1:c.410-9251_410-9242del	XP_011521407.1:n.410-9251_410-9242del
XM_011523101.3:c.410-9251_410-9242del	XP_011521403.1:n.410-9251_410-9242del
XM_011523103.3:c.410-9251_410-9242del	XP_011521405.1:n.410-9251_410-9242del
XM_011523104.3:c.410-9251_410-9242del	XP_011521406.1:n.410-9251_410-9242del
XM_011523105.3:c.410-9251_410-9242del	XP_011521407.1:n.410-9251_410-9242del
XM_017023278.2:c.410-9251_410-9242del	XP_016878767.1:n.410-9251_410-9242del
NM_016373.4:c.410-9251_410-9242del MANE Select	NP_057457.1:n.410-9251_410-9242del
NM_001291997.2:c.71-9251_71-9242del	NP_001278926.1:n.71-9251_71-9242del
NM_130791.4:c.410-9251_410-9242del	NP_570607.1:n.410-9251_410-9242del
NR_120436.2:n.649-9251_649-9242del
NM_130791.5:c.410-9251_410-9242del	NP_570607.1:n.410-9251_410-9242del
NR_120436.3:n.649-9251_649-9242del