Canonical Allele Identifier: CA2732864326

Gene: WWOX

Linked Data

• dbSNP Id: rs2151666128

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78108679_78108680del , CM000678.2:g.78108679_78108680del	GRCh38
NC_000016.9:g.78142576_78142577del , CM000678.1:g.78142576_78142577del	GRCh37
NC_000016.8:g.76700077_76700078del	NCBI36
NG_011698.1:g.14026_14027del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.172+192_172+193del	ENSP00000485925.2:n.172+192_172+193del
ENST00000682609.1:n.499+192_499+193del
ENST00000683286.1:n.499+192_499+193del
ENST00000683929.1:c.172+192_172+193del	ENSP00000507689.1:n.172+192_172+193del
ENST00000684070.1:n.437-1099_437-1098del
ENST00000684381.1:n.499+192_499+193del
ENST00000684452.1:n.499+192_499+193del
ENST00000684632.1:n.551+192_551+193del
ENST00000566780.6:c.172+192_172+193del MANE Select	ENSP00000457230.1:n.172+192_172+193del
ENST00000355860.7:c.172+192_172+193del	ENSP00000348119.3:n.172+192_172+193del
ENST00000402655.6:c.172+192_172+193del	ENSP00000384238.2:n.172+192_172+193del
ENST00000406884.6:c.172+192_172+193del	ENSP00000384495.2:n.172+192_172+193del
ENST00000408984.7:c.172+192_172+193del	ENSP00000386161.3:n.172+192_172+193del
ENST00000539474.6:c.172+192_172+193del	ENSP00000445210.2:n.172+192_172+193del
ENST00000561846.5:n.216+192_216+193del
ENST00000562214.5:n.295+192_295+193del
ENST00000563358.5:n.279+192_279+193del
ENST00000565562.5:n.217+192_217+193del
ENST00000566662.5:c.108-1099_108-1098del	ENSP00000454331.1:n.108-1099_108-1098del
ENST00000566780.5:c.172+192_172+193del	ENSP00000457230.1:n.172+192_172+193del
ENST00000569332.5:c.108-1099_108-1098del	ENSP00000454788.1:n.108-1099_108-1098del
ENST00000627394.2:c.108-1099_108-1098del	ENSP00000485925.1:n.108-1099_108-1098del
NM_001291997.1:c.-167-1099_-167-1098del	NP_001278926.1:n.-167-1099_-167-1098del
NM_016373.3:c.172+192_172+193del	NP_057457.1:n.172+192_172+193del
NM_130791.3:c.172+192_172+193del	NP_570607.1:n.172+192_172+193del
NR_120436.1:n.652+192_652+193del
XM_006721195.2:c.172+192_172+193del	XP_006721258.1:n.172+192_172+193del
XM_011523100.1:c.172+192_172+193del	XP_011521402.1:n.172+192_172+193del
XM_011523101.1:c.172+192_172+193del	XP_011521403.1:n.172+192_172+193del
XM_011523102.1:c.172+192_172+193del	XP_011521404.1:n.172+192_172+193del
XM_011523103.1:c.172+192_172+193del	XP_011521405.1:n.172+192_172+193del
XM_011523104.1:c.172+192_172+193del	XP_011521406.1:n.172+192_172+193del
XM_011523105.1:c.172+192_172+193del	XP_011521407.1:n.172+192_172+193del
XM_011523101.3:c.172+192_172+193del	XP_011521403.1:n.172+192_172+193del
XM_011523103.3:c.172+192_172+193del	XP_011521405.1:n.172+192_172+193del
XM_011523104.3:c.172+192_172+193del	XP_011521406.1:n.172+192_172+193del
XM_011523105.3:c.172+192_172+193del	XP_011521407.1:n.172+192_172+193del
XM_017023278.2:c.172+192_172+193del	XP_016878767.1:n.172+192_172+193del
NM_016373.4:c.172+192_172+193del MANE Select	NP_057457.1:n.172+192_172+193del
NM_001291997.2:c.-167-1099_-167-1098del	NP_001278926.1:n.-167-1099_-167-1098del
NM_130791.4:c.172+192_172+193del	NP_570607.1:n.172+192_172+193del
NR_120436.2:n.411+192_411+193del
NM_130791.5:c.172+192_172+193del	NP_570607.1:n.172+192_172+193del
NR_120436.3:n.411+192_411+193del