Canonical Allele Identifier: CA1877490272

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370877T= , CM000671.2:g.122370877T=	GRCh38
NC_000009.11:g.125133156T= , CM000671.1:g.125133156T=	GRCh37
NC_000009.10:g.124172977T=	NCBI36
NG_032900.1:g.4928T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+35T=	ENSP00000437709.1:n.-291+35T=
ENST00000643810.1:c.-321+35T=	ENSP00000494717.1:n.-321+35T=
ENST00000540753.5:c.-291+35T=	ENSP00000437709.1:n.-291+35T=
NM_001271166.1:c.-321+35T=	NP_001258095.1:n.-321+35T=
NM_001271368.1:c.-291+35T=	NP_001258297.1:n.-291+35T=
XM_011518875.1:c.-291+35T=	XP_011517177.1:n.-291+35T=
XM_011518876.1:c.-4153+35T=	XP_011517178.1:n.-4153+35T=
XM_011518875.2:c.-291+35T=	XP_011517177.1:n.-291+35T=
XM_011518876.2:c.-4153+35T=	XP_011517178.1:n.-4153+35T=
XM_024447614.1:c.-321+35T=	XP_024303382.1:n.-321+35T=
XM_024447615.1:c.-321+35T=	XP_024303383.1:n.-321+35T=
NM_001271166.2:c.-321+35T=	NP_001258095.1:n.-321+35T=
NM_001271368.2:c.-291+35T=	NP_001258297.1:n.-291+35T=