Canonical Allele Identifier: CA754503273

Gene: ODC1

Linked Data

• dbSNP Id: rs1321495503
• MyVariant Identifiers: chr2:g.10587978_10587989del (hg19) ; chr2:g.10447852_10447863del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447860_10447871del , CM000664.2:g.10447860_10447871del	GRCh38
NC_000002.11:g.10587986_10587997del , CM000664.1:g.10587986_10587997del	GRCh37
NC_000002.10:g.10505437_10505448del	NCBI36
NG_012105.1:g.5465_5476del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-363_-352del	ENSP00000390691.2:n.-363_-352del
ENST00000446285.6:c.-128+258_-128+269del	ENSP00000514632.1:n.-128+258_-128+269del
ENST00000699835.1:c.-807_-796del	ENSP00000514633.1:n.-807_-796del
ENST00000699836.1:c.-18+258_-18+269del	ENSP00000514634.1:n.-18+258_-18+269del
ENST00000234111.9:c.-128+258_-128+269del MANE Select	ENSP00000234111.4:n.-128+258_-128+269del
ENST00000234111.8:c.-128+258_-128+269del	ENSP00000234111.4:n.-128+258_-128+269del
ENST00000446285.5:n.189+258_189+269del
NM_001287188.1:c.-415+258_-415+269del	NP_001274117.1:n.-415+258_-415+269del
NM_002539.2:c.-128+258_-128+269del	NP_002530.1:n.-128+258_-128+269del
NM_002539.3:c.-128+258_-128+269del MANE Select	NP_002530.1:n.-128+258_-128+269del
NM_001287188.2:c.-415+258_-415+269del	NP_001274117.1:n.-415+258_-415+269del
NM_001287189.2:c.-517_-506del	NP_001274118.1:n.-517_-506del
NM_001287190.2:c.-363_-352del	NP_001274119.1:n.-363_-352del