Canonical Allele Identifier: CA467190957
Gene: PTGS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.125143759A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122381480A>G , CM000671.2:g.122381480A>G GRCh38
NC_000009.11:g.125143759A>G , CM000671.1:g.125143759A>G GRCh37
NC_000009.10:g.124183580A>G NCBI36
NG_032900.1:g.15531A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000362012.7:c.606A>G MANE Select ENSP00000354612.2:p.Gln202=
ENST00000373698.7:c.279A>G ENSP00000362802.5:p.Gln93=
ENST00000426608.6:c.313-16A>G ENSP00000411606.2:n.313-16A>G
ENST00000540753.6:c.531A>G ENSP00000437709.1:p.Gln177=
ENST00000619306.5:c.462A>G ENSP00000483540.2:p.Gln154=
ENST00000643576.1:n.700A>G
ENST00000643810.1:c.279A>G ENSP00000494717.1:p.Gln93=
ENST00000645132.1:n.519+2907A>G
ENST00000647067.1:c.*451A>G ENSP00000495728.1:n.*451A>G
ENST00000223423.8:c.606A>G ENSP00000223423.4:p.Gln202=
ENST00000362012.6:c.606A>G ENSP00000354612.2:p.Gln202=
ENST00000373698.6:c.279A>G ENSP00000362802.5:p.Gln93=
ENST00000426608.5:c.304-16A>G ENSP00000411606.1:n.304-16A>G
ENST00000540753.5:c.531A>G ENSP00000437709.1:p.Gln177=
ENST00000614910.4:c.462A>G ENSP00000484800.1:p.Gln154=
ENST00000619306.4:c.699A>G ENSP00000483540.1:p.Gln233=
NM_000962.3:c.606A>G NP_000953.2:p.Gln202=
NM_001271164.1:c.462A>G NP_001258093.1:p.Gln154=
NM_001271165.1:c.279A>G NP_001258094.1:p.Gln93=
NM_001271166.1:c.279A>G NP_001258095.1:p.Gln93=
NM_001271367.1:c.279A>G NP_001258296.1:p.Gln93=
NM_001271368.1:c.531A>G NP_001258297.1:p.Gln177=
NM_080591.2:c.606A>G NP_542158.1:p.Gln202=
XM_005252105.2:c.531A>G XP_005252162.1:p.Gln177=
XM_011518875.1:c.531A>G XP_011517177.1:p.Gln177=
XM_011518876.1:c.279A>G XP_011517178.1:p.Gln93=
XM_005252105.3:c.531A>G XP_005252162.1:p.Gln177=
XM_011518875.2:c.531A>G XP_011517177.1:p.Gln177=
XM_011518876.2:c.279A>G XP_011517178.1:p.Gln93=
XM_024447614.1:c.279A>G XP_024303382.1:p.Gln93=
XM_024447615.1:c.279A>G XP_024303383.1:p.Gln93=
NM_000962.4:c.606A>G MANE Select NP_000953.2:p.Gln202=
NM_001271164.2:c.462A>G NP_001258093.1:p.Gln154=
NM_001271165.2:c.279A>G NP_001258094.1:p.Gln93=
NM_001271166.2:c.279A>G NP_001258095.1:p.Gln93=
NM_001271367.2:c.279A>G NP_001258296.1:p.Gln93=
NM_001271368.2:c.531A>G NP_001258297.1:p.Gln177=
NM_080591.3:c.606A>G NP_542158.1:p.Gln202=