Canonical Allele Identifier: CA2732864277

Gene: WWOX

Linked Data

• dbSNP Id: rs2151666099

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78108669_78108675del , CM000678.2:g.78108669_78108675del	GRCh38
NC_000016.9:g.78142566_78142572del , CM000678.1:g.78142566_78142572del	GRCh37
NC_000016.8:g.76700067_76700073del	NCBI36
NG_011698.1:g.14016_14022del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.172+182_172+188del	ENSP00000485925.2:n.172+182_172+188del
ENST00000682609.1:n.499+182_499+188del
ENST00000683286.1:n.499+182_499+188del
ENST00000683929.1:c.172+182_172+188del	ENSP00000507689.1:n.172+182_172+188del
ENST00000684070.1:n.437-1109_437-1103del
ENST00000684381.1:n.499+182_499+188del
ENST00000684452.1:n.499+182_499+188del
ENST00000684632.1:n.551+182_551+188del
ENST00000566780.6:c.172+182_172+188del MANE Select	ENSP00000457230.1:n.172+182_172+188del
ENST00000355860.7:c.172+182_172+188del	ENSP00000348119.3:n.172+182_172+188del
ENST00000402655.6:c.172+182_172+188del	ENSP00000384238.2:n.172+182_172+188del
ENST00000406884.6:c.172+182_172+188del	ENSP00000384495.2:n.172+182_172+188del
ENST00000408984.7:c.172+182_172+188del	ENSP00000386161.3:n.172+182_172+188del
ENST00000539474.6:c.172+182_172+188del	ENSP00000445210.2:n.172+182_172+188del
ENST00000561846.5:n.216+182_216+188del
ENST00000562214.5:n.295+182_295+188del
ENST00000563358.5:n.279+182_279+188del
ENST00000565562.5:n.217+182_217+188del
ENST00000566662.5:c.108-1109_108-1103del	ENSP00000454331.1:n.108-1109_108-1103del
ENST00000566780.5:c.172+182_172+188del	ENSP00000457230.1:n.172+182_172+188del
ENST00000569332.5:c.108-1109_108-1103del	ENSP00000454788.1:n.108-1109_108-1103del
ENST00000627394.2:c.108-1109_108-1103del	ENSP00000485925.1:n.108-1109_108-1103del
NM_001291997.1:c.-167-1109_-167-1103del	NP_001278926.1:n.-167-1109_-167-1103del
NM_016373.3:c.172+182_172+188del	NP_057457.1:n.172+182_172+188del
NM_130791.3:c.172+182_172+188del	NP_570607.1:n.172+182_172+188del
NR_120436.1:n.652+182_652+188del
XM_006721195.2:c.172+182_172+188del	XP_006721258.1:n.172+182_172+188del
XM_011523100.1:c.172+182_172+188del	XP_011521402.1:n.172+182_172+188del
XM_011523101.1:c.172+182_172+188del	XP_011521403.1:n.172+182_172+188del
XM_011523102.1:c.172+182_172+188del	XP_011521404.1:n.172+182_172+188del
XM_011523103.1:c.172+182_172+188del	XP_011521405.1:n.172+182_172+188del
XM_011523104.1:c.172+182_172+188del	XP_011521406.1:n.172+182_172+188del
XM_011523105.1:c.172+182_172+188del	XP_011521407.1:n.172+182_172+188del
XM_011523101.3:c.172+182_172+188del	XP_011521403.1:n.172+182_172+188del
XM_011523103.3:c.172+182_172+188del	XP_011521405.1:n.172+182_172+188del
XM_011523104.3:c.172+182_172+188del	XP_011521406.1:n.172+182_172+188del
XM_011523105.3:c.172+182_172+188del	XP_011521407.1:n.172+182_172+188del
XM_017023278.2:c.172+182_172+188del	XP_016878767.1:n.172+182_172+188del
NM_016373.4:c.172+182_172+188del MANE Select	NP_057457.1:n.172+182_172+188del
NM_001291997.2:c.-167-1109_-167-1103del	NP_001278926.1:n.-167-1109_-167-1103del
NM_130791.4:c.172+182_172+188del	NP_570607.1:n.172+182_172+188del
NR_120436.2:n.411+182_411+188del
NM_130791.5:c.172+182_172+188del	NP_570607.1:n.172+182_172+188del
NR_120436.3:n.411+182_411+188del