Canonical Allele Identifier: CA2691550136

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122370940-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370940_122370941insT , CM000671.2:g.122370940_122370941insT	GRCh38
NC_000009.11:g.125133219_125133220insT , CM000671.1:g.125133219_125133220insT	GRCh37
NC_000009.10:g.124173040_124173041insT	NCBI36
NG_032900.1:g.4991_4992insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+98_-291+99insT	ENSP00000437709.1:n.-291+98_-291+99insT
ENST00000643810.1:c.-321+98_-321+99insT	ENSP00000494717.1:n.-321+98_-321+99insT
ENST00000540753.5:c.-291+98_-291+99insT	ENSP00000437709.1:n.-291+98_-291+99insT
NM_001271166.1:c.-321+98_-321+99insT	NP_001258095.1:n.-321+98_-321+99insT
NM_001271368.1:c.-291+98_-291+99insT	NP_001258297.1:n.-291+98_-291+99insT
XM_011518875.1:c.-291+98_-291+99insT	XP_011517177.1:n.-291+98_-291+99insT
XM_011518876.1:c.-4153+98_-4153+99insT	XP_011517178.1:n.-4153+98_-4153+99insT
XM_011518875.2:c.-291+98_-291+99insT	XP_011517177.1:n.-291+98_-291+99insT
XM_011518876.2:c.-4153+98_-4153+99insT	XP_011517178.1:n.-4153+98_-4153+99insT
XM_024447614.1:c.-321+98_-321+99insT	XP_024303382.1:n.-321+98_-321+99insT
XM_024447615.1:c.-321+98_-321+99insT	XP_024303383.1:n.-321+98_-321+99insT
NM_001271166.2:c.-321+98_-321+99insT	NP_001258095.1:n.-321+98_-321+99insT
NM_001271368.2:c.-291+98_-291+99insT	NP_001258297.1:n.-291+98_-291+99insT