Canonical Allele Identifier: CA1877490262
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122370848T= , CM000671.2:g.122370848T= GRCh38
NC_000009.11:g.125133127T= , CM000671.1:g.125133127T= GRCh37
NC_000009.10:g.124172948T= NCBI36
NG_032900.1:g.4899T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000540753.6:c.-291+6T= ENSP00000437709.1:n.-291+6T=
ENST00000643810.1:c.-321+6T= ENSP00000494717.1:n.-321+6T=
ENST00000540753.5:c.-291+6T= ENSP00000437709.1:n.-291+6T=
NM_001271166.1:c.-321+6T= NP_001258095.1:n.-321+6T=
NM_001271368.1:c.-291+6T= NP_001258297.1:n.-291+6T=
XM_011518875.1:c.-291+6T= XP_011517177.1:n.-291+6T=
XM_011518876.1:c.-4153+6T= XP_011517178.1:n.-4153+6T=
XM_011518875.2:c.-291+6T= XP_011517177.1:n.-291+6T=
XM_011518876.2:c.-4153+6T= XP_011517178.1:n.-4153+6T=
XM_024447614.1:c.-321+6T= XP_024303382.1:n.-321+6T=
XM_024447615.1:c.-321+6T= XP_024303383.1:n.-321+6T=
NM_001271166.2:c.-321+6T= NP_001258095.1:n.-321+6T=
NM_001271368.2:c.-291+6T= NP_001258297.1:n.-291+6T=