Canonical Allele Identifier: CA979334602

Gene: WWOX

Linked Data

• dbSNP Id: rs2032305868
• gnomAD v3: 16-78108672-GGAT-G
• gnomAD v4: 16-78108672-GGAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78108676_78108678del , CM000678.2:g.78108676_78108678del	GRCh38
NC_000016.9:g.78142573_78142575del , CM000678.1:g.78142573_78142575del	GRCh37
NC_000016.8:g.76700074_76700076del	NCBI36
NG_011698.1:g.14023_14025del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.172+189_172+191del	ENSP00000485925.2:n.172+189_172+191del
ENST00000682609.1:n.499+189_499+191del
ENST00000683286.1:n.499+189_499+191del
ENST00000683929.1:c.172+189_172+191del	ENSP00000507689.1:n.172+189_172+191del
ENST00000684070.1:n.437-1102_437-1100del
ENST00000684381.1:n.499+189_499+191del
ENST00000684452.1:n.499+189_499+191del
ENST00000684632.1:n.551+189_551+191del
ENST00000566780.6:c.172+189_172+191del MANE Select	ENSP00000457230.1:n.172+189_172+191del
ENST00000355860.7:c.172+189_172+191del	ENSP00000348119.3:n.172+189_172+191del
ENST00000402655.6:c.172+189_172+191del	ENSP00000384238.2:n.172+189_172+191del
ENST00000406884.6:c.172+189_172+191del	ENSP00000384495.2:n.172+189_172+191del
ENST00000408984.7:c.172+189_172+191del	ENSP00000386161.3:n.172+189_172+191del
ENST00000539474.6:c.172+189_172+191del	ENSP00000445210.2:n.172+189_172+191del
ENST00000561846.5:n.216+189_216+191del
ENST00000562214.5:n.295+189_295+191del
ENST00000563358.5:n.279+189_279+191del
ENST00000565562.5:n.217+189_217+191del
ENST00000566662.5:c.108-1102_108-1100del	ENSP00000454331.1:n.108-1102_108-1100del
ENST00000566780.5:c.172+189_172+191del	ENSP00000457230.1:n.172+189_172+191del
ENST00000569332.5:c.108-1102_108-1100del	ENSP00000454788.1:n.108-1102_108-1100del
ENST00000627394.2:c.108-1102_108-1100del	ENSP00000485925.1:n.108-1102_108-1100del
NM_001291997.1:c.-167-1102_-167-1100del	NP_001278926.1:n.-167-1102_-167-1100del
NM_016373.3:c.172+189_172+191del	NP_057457.1:n.172+189_172+191del
NM_130791.3:c.172+189_172+191del	NP_570607.1:n.172+189_172+191del
NR_120436.1:n.652+189_652+191del
XM_006721195.2:c.172+189_172+191del	XP_006721258.1:n.172+189_172+191del
XM_011523100.1:c.172+189_172+191del	XP_011521402.1:n.172+189_172+191del
XM_011523101.1:c.172+189_172+191del	XP_011521403.1:n.172+189_172+191del
XM_011523102.1:c.172+189_172+191del	XP_011521404.1:n.172+189_172+191del
XM_011523103.1:c.172+189_172+191del	XP_011521405.1:n.172+189_172+191del
XM_011523104.1:c.172+189_172+191del	XP_011521406.1:n.172+189_172+191del
XM_011523105.1:c.172+189_172+191del	XP_011521407.1:n.172+189_172+191del
XM_011523101.3:c.172+189_172+191del	XP_011521403.1:n.172+189_172+191del
XM_011523103.3:c.172+189_172+191del	XP_011521405.1:n.172+189_172+191del
XM_011523104.3:c.172+189_172+191del	XP_011521406.1:n.172+189_172+191del
XM_011523105.3:c.172+189_172+191del	XP_011521407.1:n.172+189_172+191del
XM_017023278.2:c.172+189_172+191del	XP_016878767.1:n.172+189_172+191del
NM_016373.4:c.172+189_172+191del MANE Select	NP_057457.1:n.172+189_172+191del
NM_001291997.2:c.-167-1102_-167-1100del	NP_001278926.1:n.-167-1102_-167-1100del
NM_130791.4:c.172+189_172+191del	NP_570607.1:n.172+189_172+191del
NR_120436.2:n.411+189_411+191del
NM_130791.5:c.172+189_172+191del	NP_570607.1:n.172+189_172+191del
NR_120436.3:n.411+189_411+191del