Canonical Allele Identifier: CA754503336

Gene: ODC1

Linked Data

• dbSNP Id: rs538382777
• gnomAD v3: 2-10447925-G-C
• gnomAD v4: 2-10447925-G-C
• MyVariant Identifiers: chr2:g.10588051G>C (hg19) ; chr2:g.10447925G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447925G>C , CM000664.2:g.10447925G>C	GRCh38
NC_000002.11:g.10588051G>C , CM000664.1:g.10588051G>C	GRCh37
NC_000002.10:g.10505502G>C	NCBI36
NG_012105.1:g.5403C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000443218.2:c.-425C>G	ENSP00000390691.2:n.-425C>G
ENST00000446285.6:c.-128+196C>G	ENSP00000514632.1:n.-128+196C>G
ENST00000699835.1:c.-869C>G	ENSP00000514633.1:n.-869C>G
ENST00000699836.1:c.-18+196C>G	ENSP00000514634.1:n.-18+196C>G
ENST00000234111.9:c.-128+196C>G MANE Select	ENSP00000234111.4:n.-128+196C>G
ENST00000234111.8:c.-128+196C>G	ENSP00000234111.4:n.-128+196C>G
ENST00000446285.5:n.189+196C>G
NM_001287188.1:c.-415+196C>G	NP_001274117.1:n.-415+196C>G
NM_002539.2:c.-128+196C>G	NP_002530.1:n.-128+196C>G
NM_002539.3:c.-128+196C>G MANE Select	NP_002530.1:n.-128+196C>G
NM_001287188.2:c.-415+196C>G	NP_001274117.1:n.-415+196C>G
NM_001287189.2:c.-579C>G	NP_001274118.1:n.-579C>G
NM_001287190.2:c.-425C>G	NP_001274119.1:n.-425C>G