Canonical Allele Identifier: CA1877491843

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371231C= , CM000671.2:g.122371231C=	GRCh38
NC_000009.11:g.125133510C= , CM000671.1:g.125133510C=	GRCh37
NC_000009.10:g.124173331C=	NCBI36
NG_032900.1:g.5282C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000362012.7:c.53C= MANE Select	ENSP00000354612.2:p.Pro18=
ENST00000426608.6:c.53C=	ENSP00000411606.2:p.Pro18=
ENST00000540753.6:c.-245C=	ENSP00000437709.1:n.-245C=
ENST00000619306.5:c.53C=	ENSP00000483540.2:p.Pro18=
ENST00000643576.1:n.147C=
ENST00000643810.1:c.-275C=	ENSP00000494717.1:n.-275C=
ENST00000645132.1:n.220C=
ENST00000647067.1:c.53C=	ENSP00000495728.1:p.Pro18=
ENST00000223423.8:c.53C=	ENSP00000223423.4:p.Pro18=
ENST00000362012.6:c.53C=	ENSP00000354612.2:p.Pro18=
ENST00000426608.5:c.44C=	ENSP00000411606.1:p.Pro15=
ENST00000540753.5:c.-245C=	ENSP00000437709.1:n.-245C=
ENST00000614910.4:c.53C=	ENSP00000484800.1:p.Pro18=
ENST00000619306.4:c.146C=	ENSP00000483540.1:p.Pro49=
NM_000962.3:c.53C=	NP_000953.2:p.Pro18=
NM_001271164.1:c.53C=	NP_001258093.1:p.Pro18=
NM_001271166.1:c.-275C=	NP_001258095.1:n.-275C=
NM_001271367.1:c.-246C=	NP_001258296.1:n.-246C=
NM_001271368.1:c.-245C=	NP_001258297.1:n.-245C=
NM_080591.2:c.53C=	NP_542158.1:p.Pro18=
XM_005252105.2:c.-245C=	XP_005252162.1:n.-245C=
XM_011518875.1:c.-245C=	XP_011517177.1:n.-245C=
XM_011518876.1:c.-4107C=	XP_011517178.1:n.-4107C=
XM_005252105.3:c.-245C=	XP_005252162.1:n.-245C=
XM_011518875.2:c.-245C=	XP_011517177.1:n.-245C=
XM_011518876.2:c.-4107C=	XP_011517178.1:n.-4107C=
XM_024447614.1:c.-275C=	XP_024303382.1:n.-275C=
XM_024447615.1:c.-275C=	XP_024303383.1:n.-275C=
NM_000962.4:c.53C= MANE Select	NP_000953.2:p.Pro18=
NM_001271164.2:c.53C=	NP_001258093.1:p.Pro18=
NM_001271166.2:c.-275C=	NP_001258095.1:n.-275C=
NM_001271367.2:c.-246C=	NP_001258296.1:n.-246C=
NM_001271368.2:c.-245C=	NP_001258297.1:n.-245C=
NM_080591.3:c.53C=	NP_542158.1:p.Pro18=