Canonical Allele Identifier: CA1877490367

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371012G= , CM000671.2:g.122371012G=	GRCh38
NC_000009.11:g.125133291G= , CM000671.1:g.125133291G=	GRCh37
NC_000009.10:g.124173112G=	NCBI36
NG_032900.1:g.5063G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+170G=	ENSP00000437709.1:n.-291+170G=
ENST00000643810.1:c.-321+170G=	ENSP00000494717.1:n.-321+170G=
ENST00000645132.1:n.1G=
ENST00000540753.5:c.-291+170G=	ENSP00000437709.1:n.-291+170G=
ENST00000614910.4:c.-73G=	ENSP00000484800.1:n.-73G=
NM_000962.3:c.-73G=	NP_000953.2:n.-73G=
NM_001271164.1:c.-73G=	NP_001258093.1:n.-73G=
NM_001271166.1:c.-321+170G=	NP_001258095.1:n.-321+170G=
NM_001271367.1:c.-371G=	NP_001258296.1:n.-371G=
NM_001271368.1:c.-291+170G=	NP_001258297.1:n.-291+170G=
NM_080591.2:c.-73G=	NP_542158.1:n.-73G=
XM_011518875.1:c.-291+170G=	XP_011517177.1:n.-291+170G=
XM_011518876.1:c.-4153+170G=	XP_011517178.1:n.-4153+170G=
XM_011518875.2:c.-291+170G=	XP_011517177.1:n.-291+170G=
XM_011518876.2:c.-4153+170G=	XP_011517178.1:n.-4153+170G=
XM_024447614.1:c.-321+170G=	XP_024303382.1:n.-321+170G=
XM_024447615.1:c.-321+170G=	XP_024303383.1:n.-321+170G=
NM_001271166.2:c.-321+170G=	NP_001258095.1:n.-321+170G=
NM_001271368.2:c.-291+170G=	NP_001258297.1:n.-291+170G=