Canonical Allele Identifier: CA1877490258
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122370842_122370843delinsCG , CM000671.2:g.122370842_122370843delinsCG GRCh38
NC_000009.11:g.125133121_125133122delinsCG , CM000671.1:g.125133121_125133122delinsCG GRCh37
NC_000009.10:g.124172942_124172943delinsCG NCBI36
NG_032900.1:g.4893_4894delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000540753.6:c.-291_-291+1delinsCG
ENST00000643810.1:c.-321_-321+1delinsCG
ENST00000540753.5:c.-291_-291+1delinsCG
NM_001271166.1:c.-321_-321+1delinsCG
NM_001271368.1:c.-291_-291+1delinsCG
XM_011518875.1:c.-291_-291+1delinsCG
XM_011518876.1:c.-4153_-4153+1delinsCG
XM_011518875.2:c.-291_-291+1delinsCG
XM_011518876.2:c.-4153_-4153+1delinsCG
XM_024447614.1:c.-321_-321+1delinsCG
XM_024447615.1:c.-321_-321+1delinsCG
NM_001271166.2:c.-321_-321+1delinsCG
NM_001271368.2:c.-291_-291+1delinsCG