Canonical Allele Identifier: CA1877496546
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122381388G= , CM000671.2:g.122381388G= GRCh38
NC_000009.11:g.125143667G= , CM000671.1:g.125143667G= GRCh37
NC_000009.10:g.124183488G= NCBI36
NG_032900.1:g.15439G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362012.7:c.514G= MANE Select ENSP00000354612.2:p.Asp172=
ENST00000373698.7:c.187G= ENSP00000362802.5:p.Asp63=
ENST00000426608.6:c.313-108G= ENSP00000411606.2:n.313-108G=
ENST00000540753.6:c.439G= ENSP00000437709.1:p.Asp147=
ENST00000619306.5:c.370G= ENSP00000483540.2:p.Asp124=
ENST00000643576.1:n.608G=
ENST00000643810.1:c.187G= ENSP00000494717.1:p.Asp63=
ENST00000645132.1:n.519+2815G=
ENST00000647067.1:c.*359G= ENSP00000495728.1:n.*359G=
ENST00000223423.8:c.514G= ENSP00000223423.4:p.Asp172=
ENST00000362012.6:c.514G= ENSP00000354612.2:p.Asp172=
ENST00000373698.6:c.187G= ENSP00000362802.5:p.Asp63=
ENST00000426608.5:c.304-108G= ENSP00000411606.1:n.304-108G=
ENST00000540753.5:c.439G= ENSP00000437709.1:p.Asp147=
ENST00000614910.4:c.370G= ENSP00000484800.1:p.Asp124=
ENST00000619306.4:c.607G= ENSP00000483540.1:p.Asp203=
NM_000962.3:c.514G= NP_000953.2:p.Asp172=
NM_001271164.1:c.370G= NP_001258093.1:p.Asp124=
NM_001271165.1:c.187G= NP_001258094.1:p.Asp63=
NM_001271166.1:c.187G= NP_001258095.1:p.Asp63=
NM_001271367.1:c.187G= NP_001258296.1:p.Asp63=
NM_001271368.1:c.439G= NP_001258297.1:p.Asp147=
NM_080591.2:c.514G= NP_542158.1:p.Asp172=
XM_005252105.2:c.439G= XP_005252162.1:p.Asp147=
XM_011518875.1:c.439G= XP_011517177.1:p.Asp147=
XM_011518876.1:c.187G= XP_011517178.1:p.Asp63=
XM_005252105.3:c.439G= XP_005252162.1:p.Asp147=
XM_011518875.2:c.439G= XP_011517177.1:p.Asp147=
XM_011518876.2:c.187G= XP_011517178.1:p.Asp63=
XM_024447614.1:c.187G= XP_024303382.1:p.Asp63=
XM_024447615.1:c.187G= XP_024303383.1:p.Asp63=
NM_000962.4:c.514G= MANE Select NP_000953.2:p.Asp172=
NM_001271164.2:c.370G= NP_001258093.1:p.Asp124=
NM_001271165.2:c.187G= NP_001258094.1:p.Asp63=
NM_001271166.2:c.187G= NP_001258095.1:p.Asp63=
NM_001271367.2:c.187G= NP_001258296.1:p.Asp63=
NM_001271368.2:c.439G= NP_001258297.1:p.Asp147=
NM_080591.3:c.514G= NP_542158.1:p.Asp172=