Canonical Allele Identifier: CA2657843920

Gene: ODC1

Linked Data

• gnomAD v4: 2-10447933-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447933T>C , CM000664.2:g.10447933T>C	GRCh38
NC_000002.11:g.10588059T>C , CM000664.1:g.10588059T>C	GRCh37
NC_000002.10:g.10505510T>C	NCBI36
NG_012105.1:g.5395A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-433A>G	ENSP00000390691.2:n.-433A>G
ENST00000446285.6:c.-128+188A>G	ENSP00000514632.1:n.-128+188A>G
ENST00000699835.1:c.-877A>G	ENSP00000514633.1:n.-877A>G
ENST00000699836.1:c.-18+188A>G	ENSP00000514634.1:n.-18+188A>G
ENST00000234111.9:c.-128+188A>G MANE Select	ENSP00000234111.4:n.-128+188A>G
ENST00000234111.8:c.-128+188A>G	ENSP00000234111.4:n.-128+188A>G
ENST00000446285.5:n.189+188A>G
NM_001287188.1:c.-415+188A>G	NP_001274117.1:n.-415+188A>G
NM_002539.2:c.-128+188A>G	NP_002530.1:n.-128+188A>G
NM_002539.3:c.-128+188A>G MANE Select	NP_002530.1:n.-128+188A>G
NM_001287188.2:c.-415+188A>G	NP_001274117.1:n.-415+188A>G
NM_001287189.2:c.-587A>G	NP_001274118.1:n.-587A>G
NM_001287190.2:c.-433A>G	NP_001274119.1:n.-433A>G