Canonical Allele Identifier: CA1877490375
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122371016C= , CM000671.2:g.122371016C= GRCh38
NC_000009.11:g.125133295C= , CM000671.1:g.125133295C= GRCh37
NC_000009.10:g.124173116C= NCBI36
NG_032900.1:g.5067C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000540753.6:c.-290-170C= ENSP00000437709.1:n.-290-170C=
ENST00000643810.1:c.-320-170C= ENSP00000494717.1:n.-320-170C=
ENST00000645132.1:n.5C=
ENST00000540753.5:c.-290-170C= ENSP00000437709.1:n.-290-170C=
ENST00000614910.4:c.-69C= ENSP00000484800.1:n.-69C=
NM_000962.3:c.-69C= NP_000953.2:n.-69C=
NM_001271164.1:c.-69C= NP_001258093.1:n.-69C=
NM_001271166.1:c.-320-170C= NP_001258095.1:n.-320-170C=
NM_001271367.1:c.-367C= NP_001258296.1:n.-367C=
NM_001271368.1:c.-290-170C= NP_001258297.1:n.-290-170C=
NM_080591.2:c.-69C= NP_542158.1:n.-69C=
XM_011518875.1:c.-290-170C= XP_011517177.1:n.-290-170C=
XM_011518876.1:c.-4152-170C= XP_011517178.1:n.-4152-170C=
XM_011518875.2:c.-290-170C= XP_011517177.1:n.-290-170C=
XM_011518876.2:c.-4152-170C= XP_011517178.1:n.-4152-170C=
XM_024447614.1:c.-320-170C= XP_024303382.1:n.-320-170C=
XM_024447615.1:c.-320-170C= XP_024303383.1:n.-320-170C=
NM_001271166.2:c.-320-170C= NP_001258095.1:n.-320-170C=
NM_001271368.2:c.-290-170C= NP_001258297.1:n.-290-170C=