Canonical Allele Identifier: CA42456807

Gene: ODC1

Linked Data

• dbSNP Id: rs1022947813
• gnomAD v3: 2-10447824-T-C
• gnomAD v4: 2-10447824-T-C
• MyVariant Identifiers: chr2:g.10587950T>C (hg19) ; chr2:g.10447824T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447824T>C , CM000664.2:g.10447824T>C	GRCh38
NC_000002.11:g.10587950T>C , CM000664.1:g.10587950T>C	GRCh37
NC_000002.10:g.10505401T>C	NCBI36
NG_012105.1:g.5504A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-324A>G	ENSP00000390691.2:n.-324A>G
ENST00000446285.6:c.-128+297A>G	ENSP00000514632.1:n.-128+297A>G
ENST00000699835.1:c.-768A>G	ENSP00000514633.1:n.-768A>G
ENST00000699836.1:c.-18+297A>G	ENSP00000514634.1:n.-18+297A>G
ENST00000234111.9:c.-128+297A>G MANE Select	ENSP00000234111.4:n.-128+297A>G
ENST00000234111.8:c.-128+297A>G	ENSP00000234111.4:n.-128+297A>G
ENST00000446285.5:n.189+297A>G
NM_001287188.1:c.-415+297A>G	NP_001274117.1:n.-415+297A>G
NM_002539.2:c.-128+297A>G	NP_002530.1:n.-128+297A>G
NM_002539.3:c.-128+297A>G MANE Select	NP_002530.1:n.-128+297A>G
NM_001287188.2:c.-415+297A>G	NP_001274117.1:n.-415+297A>G
NM_001287189.2:c.-478A>G	NP_001274118.1:n.-478A>G
NM_001287190.2:c.-324A>G	NP_001274119.1:n.-324A>G