Canonical Allele Identifier: CA1877496585
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122381490C= , CM000671.2:g.122381490C= GRCh38
NC_000009.11:g.125143769C= , CM000671.1:g.125143769C= GRCh37
NC_000009.10:g.124183590C= NCBI36
NG_032900.1:g.15541C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362012.7:c.616C= MANE Select ENSP00000354612.2:p.His206=
ENST00000373698.7:c.289C= ENSP00000362802.5:p.His97=
ENST00000426608.6:c.313-6C= ENSP00000411606.2:n.313-6C=
ENST00000540753.6:c.541C= ENSP00000437709.1:p.His181=
ENST00000619306.5:c.472C= ENSP00000483540.2:p.His158=
ENST00000643576.1:n.710C=
ENST00000643810.1:c.289C= ENSP00000494717.1:p.His97=
ENST00000645132.1:n.519+2917C=
ENST00000647067.1:c.*461C= ENSP00000495728.1:n.*461C=
ENST00000223423.8:c.616C= ENSP00000223423.4:p.His206=
ENST00000362012.6:c.616C= ENSP00000354612.2:p.His206=
ENST00000373698.6:c.289C= ENSP00000362802.5:p.His97=
ENST00000426608.5:c.304-6C= ENSP00000411606.1:n.304-6C=
ENST00000540753.5:c.541C= ENSP00000437709.1:p.His181=
ENST00000614910.4:c.472C= ENSP00000484800.1:p.His158=
ENST00000619306.4:c.709C= ENSP00000483540.1:p.His237=
NM_000962.3:c.616C= NP_000953.2:p.His206=
NM_001271164.1:c.472C= NP_001258093.1:p.His158=
NM_001271165.1:c.289C= NP_001258094.1:p.His97=
NM_001271166.1:c.289C= NP_001258095.1:p.His97=
NM_001271367.1:c.289C= NP_001258296.1:p.His97=
NM_001271368.1:c.541C= NP_001258297.1:p.His181=
NM_080591.2:c.616C= NP_542158.1:p.His206=
XM_005252105.2:c.541C= XP_005252162.1:p.His181=
XM_011518875.1:c.541C= XP_011517177.1:p.His181=
XM_011518876.1:c.289C= XP_011517178.1:p.His97=
XM_005252105.3:c.541C= XP_005252162.1:p.His181=
XM_011518875.2:c.541C= XP_011517177.1:p.His181=
XM_011518876.2:c.289C= XP_011517178.1:p.His97=
XM_024447614.1:c.289C= XP_024303382.1:p.His97=
XM_024447615.1:c.289C= XP_024303383.1:p.His97=
NM_000962.4:c.616C= MANE Select NP_000953.2:p.His206=
NM_001271164.2:c.472C= NP_001258093.1:p.His158=
NM_001271165.2:c.289C= NP_001258094.1:p.His97=
NM_001271166.2:c.289C= NP_001258095.1:p.His97=
NM_001271367.2:c.289C= NP_001258296.1:p.His97=
NM_001271368.2:c.541C= NP_001258297.1:p.His181=
NM_080591.3:c.616C= NP_542158.1:p.His206=