Canonical Allele Identifier: CA1027506498

Gene: ODC1

Linked Data

• dbSNP Id: rs1672081391
• gnomAD v3: 2-10447831-A-G
• gnomAD v4: 2-10447831-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447831A>G , CM000664.2:g.10447831A>G	GRCh38
NC_000002.11:g.10587957A>G , CM000664.1:g.10587957A>G	GRCh37
NC_000002.10:g.10505408A>G	NCBI36
NG_012105.1:g.5497T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-331T>C	ENSP00000390691.2:n.-331T>C
ENST00000446285.6:c.-128+290T>C	ENSP00000514632.1:n.-128+290T>C
ENST00000699835.1:c.-775T>C	ENSP00000514633.1:n.-775T>C
ENST00000699836.1:c.-18+290T>C	ENSP00000514634.1:n.-18+290T>C
ENST00000234111.9:c.-128+290T>C MANE Select	ENSP00000234111.4:n.-128+290T>C
ENST00000234111.8:c.-128+290T>C	ENSP00000234111.4:n.-128+290T>C
ENST00000446285.5:n.189+290T>C
NM_001287188.1:c.-415+290T>C	NP_001274117.1:n.-415+290T>C
NM_002539.2:c.-128+290T>C	NP_002530.1:n.-128+290T>C
NM_002539.3:c.-128+290T>C MANE Select	NP_002530.1:n.-128+290T>C
NM_001287188.2:c.-415+290T>C	NP_001274117.1:n.-415+290T>C
NM_001287189.2:c.-485T>C	NP_001274118.1:n.-485T>C
NM_001287190.2:c.-331T>C	NP_001274119.1:n.-331T>C