Canonical Allele Identifier: CA1877490444
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122371061G= , CM000671.2:g.122371061G= GRCh38
NC_000009.11:g.125133340G= , CM000671.1:g.125133340G= GRCh37
NC_000009.10:g.124173161G= NCBI36
NG_032900.1:g.5112G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362012.7:c.-24G= MANE Select ENSP00000354612.2:n.-24G=
ENST00000540753.6:c.-290-125G= ENSP00000437709.1:n.-290-125G=
ENST00000619306.5:c.-24G= ENSP00000483540.2:n.-24G=
ENST00000643810.1:c.-320-125G= ENSP00000494717.1:n.-320-125G=
ENST00000645132.1:n.50G=
ENST00000647067.1:c.-24G= ENSP00000495728.1:n.-24G=
ENST00000540753.5:c.-290-125G= ENSP00000437709.1:n.-290-125G=
ENST00000614910.4:c.-24G= ENSP00000484800.1:n.-24G=
NM_000962.3:c.-24G= NP_000953.2:n.-24G=
NM_001271164.1:c.-24G= NP_001258093.1:n.-24G=
NM_001271166.1:c.-320-125G= NP_001258095.1:n.-320-125G=
NM_001271367.1:c.-322G= NP_001258296.1:n.-322G=
NM_001271368.1:c.-290-125G= NP_001258297.1:n.-290-125G=
NM_080591.2:c.-24G= NP_542158.1:n.-24G=
XM_005252105.2:c.-321G= XP_005252162.1:n.-321G=
XM_011518875.1:c.-290-125G= XP_011517177.1:n.-290-125G=
XM_011518876.1:c.-4152-125G= XP_011517178.1:n.-4152-125G=
XM_005252105.3:c.-321G= XP_005252162.1:n.-321G=
XM_011518875.2:c.-290-125G= XP_011517177.1:n.-290-125G=
XM_011518876.2:c.-4152-125G= XP_011517178.1:n.-4152-125G=
XM_024447614.1:c.-320-125G= XP_024303382.1:n.-320-125G=
XM_024447615.1:c.-320-125G= XP_024303383.1:n.-320-125G=
NM_000962.4:c.-24G= MANE Select NP_000953.2:n.-24G=
NM_001271164.2:c.-24G= NP_001258093.1:n.-24G=
NM_001271166.2:c.-320-125G= NP_001258095.1:n.-320-125G=
NM_001271367.2:c.-322G= NP_001258296.1:n.-322G=
NM_001271368.2:c.-290-125G= NP_001258297.1:n.-290-125G=
NM_080591.3:c.-24G= NP_542158.1:n.-24G=