Canonical Allele Identifier: CA2234888522

Gene: WWOX

Linked Data

• dbSNP Id: rs2031591582

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099484_78099485del , CM000678.2:g.78099484_78099485del	GRCh38
NC_000016.9:g.78133381_78133382del , CM000678.1:g.78133381_78133382del	GRCh37
NC_000016.8:g.76690882_76690883del	NCBI36
NG_011698.1:g.4831_4832del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-295_-294del	ENSP00000485925.2:n.-295_-294del
ENST00000682609.1:n.33_34del
ENST00000683286.1:n.33_34del
ENST00000683929.1:c.-295_-294del	ENSP00000507689.1:n.-295_-294del
ENST00000684070.1:n.35_36del
ENST00000684381.1:n.33_34del
ENST00000684452.1:n.33_34del
ENST00000684632.1:n.85_86del
ENST00000566780.5:c.-295_-294del	ENSP00000457230.1:n.-295_-294del
ENST00000627394.2:c.-295_-294del	ENSP00000485925.1:n.-295_-294del
NM_001291997.1:c.-569_-568del	NP_001278926.1:n.-569_-568del
NM_016373.3:c.-295_-294del	NP_057457.1:n.-295_-294del
NM_130791.3:c.-295_-294del	NP_570607.1:n.-295_-294del
NR_120435.1:n.72_73del
NR_120436.1:n.72_73del