Canonical Allele Identifier: CA754503035

Gene: ODC1

Linked Data

• dbSNP Id: rs1240156203
• gnomAD v3: 2-10447533-C-CGAGTCA
• gnomAD v4: 2-10447533-C-CGAGTCA
• MyVariant Identifiers: chr2:g.10587659_10587660insGAGTCA (hg19) ; chr2:g.10447533_10447534insGAGTCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447534_10447539dup , CM000664.2:g.10447534_10447539dup	GRCh38
NC_000002.11:g.10587660_10587665dup , CM000664.1:g.10587660_10587665dup	GRCh37
NC_000002.10:g.10505111_10505116dup	NCBI36
NG_012105.1:g.5789_5794dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-128+89_-128+94dup	ENSP00000390691.2:n.-128+89_-128+94dup
ENST00000446285.6:c.-128+582_-128+587dup	ENSP00000514632.1:n.-128+582_-128+587dup
ENST00000699835.1:c.-483_-478dup	ENSP00000514633.1:n.-483_-478dup
ENST00000699836.1:c.-18+582_-18+587dup	ENSP00000514634.1:n.-18+582_-18+587dup
ENST00000234111.9:c.-128+582_-128+587dup MANE Select	ENSP00000234111.4:n.-128+582_-128+587dup
ENST00000234111.8:c.-128+582_-128+587dup	ENSP00000234111.4:n.-128+582_-128+587dup
ENST00000405333.5:c.-193_-188dup	ENSP00000385333.1:n.-193_-188dup
ENST00000443218.1:c.-128+89_-128+94dup	ENSP00000390691.1:n.-128+89_-128+94dup
ENST00000446285.5:n.189+582_189+587dup
NM_001287188.1:c.-415+582_-415+587dup	NP_001274117.1:n.-415+582_-415+587dup
NM_001287189.1:c.-193_-188dup	NP_001274118.1:n.-193_-188dup
NM_001287190.1:c.-128+89_-128+94dup	NP_001274119.1:n.-128+89_-128+94dup
NM_002539.2:c.-128+582_-128+587dup	NP_002530.1:n.-128+582_-128+587dup
NM_002539.3:c.-128+582_-128+587dup MANE Select	NP_002530.1:n.-128+582_-128+587dup
NM_001287188.2:c.-415+582_-415+587dup	NP_001274117.1:n.-415+582_-415+587dup
NM_001287189.2:c.-193_-188dup	NP_001274118.1:n.-193_-188dup
NM_001287190.2:c.-128+89_-128+94dup	NP_001274119.1:n.-128+89_-128+94dup