Canonical Allele Identifier: CA42456977

Gene: ODC1

Linked Data

• dbSNP Id: rs919080696
• gnomAD v3: 2-10447979-A-C
• gnomAD v4: 2-10447979-A-C
• MyVariant Identifiers: chr2:g.10588105A>C (hg19) ; chr2:g.10447979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447979A>C , CM000664.2:g.10447979A>C	GRCh38
NC_000002.11:g.10588105A>C , CM000664.1:g.10588105A>C	GRCh37
NC_000002.10:g.10505556A>C	NCBI36
NG_012105.1:g.5349T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-479T>G	ENSP00000390691.2:n.-479T>G
ENST00000446285.6:c.-128+142T>G	ENSP00000514632.1:n.-128+142T>G
ENST00000699835.1:c.-923T>G	ENSP00000514633.1:n.-923T>G
ENST00000699836.1:c.-18+142T>G	ENSP00000514634.1:n.-18+142T>G
ENST00000234111.9:c.-128+142T>G MANE Select	ENSP00000234111.4:n.-128+142T>G
ENST00000234111.8:c.-128+142T>G	ENSP00000234111.4:n.-128+142T>G
ENST00000446285.5:n.189+142T>G
NM_001287188.1:c.-415+142T>G	NP_001274117.1:n.-415+142T>G
NM_002539.2:c.-128+142T>G	NP_002530.1:n.-128+142T>G
NM_002539.3:c.-128+142T>G MANE Select	NP_002530.1:n.-128+142T>G
NM_001287188.2:c.-415+142T>G	NP_001274117.1:n.-415+142T>G
NM_001287189.2:c.-633T>G	NP_001274118.1:n.-633T>G
NM_001287190.2:c.-479T>G	NP_001274119.1:n.-479T>G