Canonical Allele Identifier: CA2657843876

Gene: ODC1

Linked Data

• gnomAD v4: 2-10447851-A-AGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447852_10447853insCTG , CM000664.2:g.10447852_10447853insCTG	GRCh38
NC_000002.11:g.10587978_10587979insCTG , CM000664.1:g.10587978_10587979insCTG	GRCh37
NC_000002.10:g.10505429_10505430insCTG	NCBI36
NG_012105.1:g.5476_5477insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-352_-351insAGC	ENSP00000390691.2:n.-352_-351insAGC
ENST00000446285.6:c.-128+269_-128+270insAGC	ENSP00000514632.1:n.-128+269_-128+270insAGC
ENST00000699835.1:c.-796_-795insAGC	ENSP00000514633.1:n.-796_-795insAGC
ENST00000699836.1:c.-18+269_-18+270insAGC	ENSP00000514634.1:n.-18+269_-18+270insAGC
ENST00000234111.9:c.-128+269_-128+270insAGC MANE Select	ENSP00000234111.4:n.-128+269_-128+270insAGC
ENST00000234111.8:c.-128+269_-128+270insAGC	ENSP00000234111.4:n.-128+269_-128+270insAGC
ENST00000446285.5:n.189+269_189+270insAGC
NM_001287188.1:c.-415+269_-415+270insAGC	NP_001274117.1:n.-415+269_-415+270insAGC
NM_002539.2:c.-128+269_-128+270insAGC	NP_002530.1:n.-128+269_-128+270insAGC
NM_002539.3:c.-128+269_-128+270insAGC MANE Select	NP_002530.1:n.-128+269_-128+270insAGC
NM_001287188.2:c.-415+269_-415+270insAGC	NP_001274117.1:n.-415+269_-415+270insAGC
NM_001287189.2:c.-506_-505insAGC	NP_001274118.1:n.-506_-505insAGC
NM_001287190.2:c.-352_-351insAGC	NP_001274119.1:n.-352_-351insAGC