Canonical Allele Identifier: CA1877491841
Community Standard Title: NM_000962.4(PTGS1):c.50C= (p.Pro17=)
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122371228C= , CM000671.2:g.122371228C= GRCh38
NC_000009.11:g.125133507C= , CM000671.1:g.125133507C= GRCh37
NC_000009.10:g.124173328C= NCBI36
NG_032900.1:g.5279C=

Transcript Alleles

HGVS Amino-acid Change
NM_000962.4:c.50C= MANE Select NP_000953.2:p.Pro17=
ENST00000362012.7:c.50C= MANE Select ENSP00000354612.2:p.Pro17=
NM_000962.3:c.50C= NP_000953.2:p.Pro17=
NM_001271164.1:c.50C= NP_001258093.1:p.Pro17=
NM_001271164.2:c.50C= NP_001258093.1:p.Pro17=
NM_001271166.1:c.-278C= NP_001258095.1:n.-278C=
NM_001271166.2:c.-278C= NP_001258095.1:n.-278C=
NM_001271367.1:c.-249C= NP_001258296.1:n.-249C=
NM_001271367.2:c.-249C= NP_001258296.1:n.-249C=
NM_001271368.1:c.-248C= NP_001258297.1:n.-248C=
NM_001271368.2:c.-248C= NP_001258297.1:n.-248C=
NM_080591.2:c.50C= NP_542158.1:p.Pro17=
NM_080591.3:c.50C= NP_542158.1:p.Pro17=
ENST00000223423.8:c.50C= ENSP00000223423.4:p.Pro17=
ENST00000362012.6:c.50C= ENSP00000354612.2:p.Pro17=
ENST00000426608.5:c.41C= ENSP00000411606.1:p.Pro14=
ENST00000426608.6:c.50C= ENSP00000411606.2:p.Pro17=
ENST00000540753.5:c.-248C= ENSP00000437709.1:n.-248C=
ENST00000540753.6:c.-248C= ENSP00000437709.1:n.-248C=
ENST00000614910.4:c.50C= ENSP00000484800.1:p.Pro17=
ENST00000619306.4:c.143C= ENSP00000483540.1:p.Pro48=
ENST00000619306.5:c.50C= ENSP00000483540.2:p.Pro17=
ENST00000643576.1:n.144C=
ENST00000643810.1:c.-278C= ENSP00000494717.1:n.-278C=
ENST00000645132.1:n.217C=
ENST00000647067.1:c.50C= ENSP00000495728.1:p.Pro17=
XM_005252105.2:c.-248C= XP_005252162.1:n.-248C=
XM_005252105.3:c.-248C= XP_005252162.1:n.-248C=
XM_011518875.1:c.-248C= XP_011517177.1:n.-248C=
XM_011518875.2:c.-248C= XP_011517177.1:n.-248C=
XM_011518876.1:c.-4110C= XP_011517178.1:n.-4110C=
XM_011518876.2:c.-4110C= XP_011517178.1:n.-4110C=
XM_024447614.1:c.-278C= XP_024303382.1:n.-278C=
XM_024447615.1:c.-278C= XP_024303383.1:n.-278C=