Canonical Allele Identifier: CA2488522712
Gene: ODC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10448131_10448140delinsCCAGGCGCCG , CM000664.2:g.10448131_10448140delinsCCAGGCGCCG GRCh38
NC_000002.11:g.10588257_10588266delinsCCAGGCGCCG , CM000664.1:g.10588257_10588266delinsCCAGGCGCCG GRCh37
NC_000002.10:g.10505708_10505717delinsCCAGGCGCCG NCBI36
NG_012105.1:g.5188_5197delinsCGGCGCCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000446285.6:c.-147_-138delinsCGGCGCCTGG ENSP00000514632.1:n.-147_-138delinsCGGCGCCTGG
ENST00000699836.1:c.-37_-28delinsCGGCGCCTGG ENSP00000514634.1:n.-37_-28delinsCGGCGCCTGG
ENST00000234111.9:c.-147_-138delinsCGGCGCCTGG MANE Select ENSP00000234111.4:n.-147_-138delinsCGGCGCCTGG
ENST00000234111.8:c.-147_-138delinsCGGCGCCTGG ENSP00000234111.4:n.-147_-138delinsCGGCGCCTGG
ENST00000446285.5:n.170_179delinsCGGCGCCTGG
NM_001287188.1:c.-434_-425delinsCGGCGCCTGG NP_001274117.1:n.-434_-425delinsCGGCGCCTGG
NM_002539.2:c.-147_-138delinsCGGCGCCTGG NP_002530.1:n.-147_-138delinsCGGCGCCTGG
NM_002539.3:c.-147_-138delinsCGGCGCCTGG MANE Select NP_002530.1:n.-147_-138delinsCGGCGCCTGG
NM_001287188.2:c.-434_-425delinsCGGCGCCTGG NP_001274117.1:n.-434_-425delinsCGGCGCCTGG