Canonical Allele Identifier: CA1877490399

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371037C= , CM000671.2:g.122371037C=	GRCh38
NC_000009.11:g.125133316C= , CM000671.1:g.125133316C=	GRCh37
NC_000009.10:g.124173137C=	NCBI36
NG_032900.1:g.5088C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.-48C= MANE Select	ENSP00000354612.2:n.-48C=
ENST00000540753.6:c.-290-149C=	ENSP00000437709.1:n.-290-149C=
ENST00000643810.1:c.-320-149C=	ENSP00000494717.1:n.-320-149C=
ENST00000645132.1:n.26C=
ENST00000647067.1:c.-48C=	ENSP00000495728.1:n.-48C=
ENST00000540753.5:c.-290-149C=	ENSP00000437709.1:n.-290-149C=
ENST00000614910.4:c.-48C=	ENSP00000484800.1:n.-48C=
NM_000962.3:c.-48C=	NP_000953.2:n.-48C=
NM_001271164.1:c.-48C=	NP_001258093.1:n.-48C=
NM_001271166.1:c.-320-149C=	NP_001258095.1:n.-320-149C=
NM_001271367.1:c.-346C=	NP_001258296.1:n.-346C=
NM_001271368.1:c.-290-149C=	NP_001258297.1:n.-290-149C=
NM_080591.2:c.-48C=	NP_542158.1:n.-48C=
XM_011518875.1:c.-290-149C=	XP_011517177.1:n.-290-149C=
XM_011518876.1:c.-4152-149C=	XP_011517178.1:n.-4152-149C=
XM_011518875.2:c.-290-149C=	XP_011517177.1:n.-290-149C=
XM_011518876.2:c.-4152-149C=	XP_011517178.1:n.-4152-149C=
XM_024447614.1:c.-320-149C=	XP_024303382.1:n.-320-149C=
XM_024447615.1:c.-320-149C=	XP_024303383.1:n.-320-149C=
NM_000962.4:c.-48C= MANE Select	NP_000953.2:n.-48C=
NM_001271164.2:c.-48C=	NP_001258093.1:n.-48C=
NM_001271166.2:c.-320-149C=	NP_001258095.1:n.-320-149C=
NM_001271367.2:c.-346C=	NP_001258296.1:n.-346C=
NM_001271368.2:c.-290-149C=	NP_001258297.1:n.-290-149C=
NM_080591.3:c.-48C=	NP_542158.1:n.-48C=