Canonical Allele Identifier: CA1877490255
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122370828C= , CM000671.2:g.122370828C= GRCh38
NC_000009.11:g.125133107C= , CM000671.1:g.125133107C= GRCh37
NC_000009.10:g.124172928C= NCBI36
NG_032900.1:g.4879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000540753.6:c.-305C= ENSP00000437709.1:n.-305C=
ENST00000643810.1:c.-335C= ENSP00000494717.1:n.-335C=
ENST00000540753.5:c.-305C= ENSP00000437709.1:n.-305C=
NM_001271166.1:c.-335C= NP_001258095.1:n.-335C=
NM_001271368.1:c.-305C= NP_001258297.1:n.-305C=
XM_011518875.1:c.-305C= XP_011517177.1:n.-305C=
XM_011518876.1:c.-4167C= XP_011517178.1:n.-4167C=
XM_011518875.2:c.-305C= XP_011517177.1:n.-305C=
XM_011518876.2:c.-4167C= XP_011517178.1:n.-4167C=
XM_024447614.1:c.-335C= XP_024303382.1:n.-335C=
XM_024447615.1:c.-335C= XP_024303383.1:n.-335C=
NM_001271166.2:c.-335C= NP_001258095.1:n.-335C=
NM_001271368.2:c.-305C= NP_001258297.1:n.-305C=