Canonical Allele Identifier: CA1877496541
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122381379C= , CM000671.2:g.122381379C= GRCh38
NC_000009.11:g.125143658C= , CM000671.1:g.125143658C= GRCh37
NC_000009.10:g.124183479C= NCBI36
NG_032900.1:g.15430C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362012.7:c.505C= MANE Select ENSP00000354612.2:p.Gln169=
ENST00000373698.7:c.178C= ENSP00000362802.5:p.Gln60=
ENST00000426608.6:c.313-117C= ENSP00000411606.2:n.313-117C=
ENST00000540753.6:c.430C= ENSP00000437709.1:p.Gln144=
ENST00000619306.5:c.361C= ENSP00000483540.2:p.Gln121=
ENST00000643576.1:n.599C=
ENST00000643810.1:c.178C= ENSP00000494717.1:p.Gln60=
ENST00000645132.1:n.519+2806C=
ENST00000647067.1:c.*350C= ENSP00000495728.1:n.*350C=
ENST00000223423.8:c.505C= ENSP00000223423.4:p.Gln169=
ENST00000362012.6:c.505C= ENSP00000354612.2:p.Gln169=
ENST00000373698.6:c.178C= ENSP00000362802.5:p.Gln60=
ENST00000426608.5:c.304-117C= ENSP00000411606.1:n.304-117C=
ENST00000540753.5:c.430C= ENSP00000437709.1:p.Gln144=
ENST00000614910.4:c.361C= ENSP00000484800.1:p.Gln121=
ENST00000619306.4:c.598C= ENSP00000483540.1:p.Gln200=
NM_000962.3:c.505C= NP_000953.2:p.Gln169=
NM_001271164.1:c.361C= NP_001258093.1:p.Gln121=
NM_001271165.1:c.178C= NP_001258094.1:p.Gln60=
NM_001271166.1:c.178C= NP_001258095.1:p.Gln60=
NM_001271367.1:c.178C= NP_001258296.1:p.Gln60=
NM_001271368.1:c.430C= NP_001258297.1:p.Gln144=
NM_080591.2:c.505C= NP_542158.1:p.Gln169=
XM_005252105.2:c.430C= XP_005252162.1:p.Gln144=
XM_011518875.1:c.430C= XP_011517177.1:p.Gln144=
XM_011518876.1:c.178C= XP_011517178.1:p.Gln60=
XM_005252105.3:c.430C= XP_005252162.1:p.Gln144=
XM_011518875.2:c.430C= XP_011517177.1:p.Gln144=
XM_011518876.2:c.178C= XP_011517178.1:p.Gln60=
XM_024447614.1:c.178C= XP_024303382.1:p.Gln60=
XM_024447615.1:c.178C= XP_024303383.1:p.Gln60=
NM_000962.4:c.505C= MANE Select NP_000953.2:p.Gln169=
NM_001271164.2:c.361C= NP_001258093.1:p.Gln121=
NM_001271165.2:c.178C= NP_001258094.1:p.Gln60=
NM_001271166.2:c.178C= NP_001258095.1:p.Gln60=
NM_001271367.2:c.178C= NP_001258296.1:p.Gln60=
NM_001271368.2:c.430C= NP_001258297.1:p.Gln144=
NM_080591.3:c.505C= NP_542158.1:p.Gln169=