Canonical Allele Identifier: CA1877490292

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370922_122370923delinsCT , CM000671.2:g.122370922_122370923delinsCT	GRCh38
NC_000009.11:g.125133201_125133202delinsCT , CM000671.1:g.125133201_125133202delinsCT	GRCh37
NC_000009.10:g.124173022_124173023delinsCT	NCBI36
NG_032900.1:g.4973_4974delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+80_-291+81delinsCT	ENSP00000437709.1:n.-291+80_-291+81delinsCT
ENST00000643810.1:c.-321+80_-321+81delinsCT	ENSP00000494717.1:n.-321+80_-321+81delinsCT
ENST00000540753.5:c.-291+80_-291+81delinsCT	ENSP00000437709.1:n.-291+80_-291+81delinsCT
NM_001271166.1:c.-321+80_-321+81delinsCT	NP_001258095.1:n.-321+80_-321+81delinsCT
NM_001271368.1:c.-291+80_-291+81delinsCT	NP_001258297.1:n.-291+80_-291+81delinsCT
XM_011518875.1:c.-291+80_-291+81delinsCT	XP_011517177.1:n.-291+80_-291+81delinsCT
XM_011518876.1:c.-4153+80_-4153+81delinsCT	XP_011517178.1:n.-4153+80_-4153+81delinsCT
XM_011518875.2:c.-291+80_-291+81delinsCT	XP_011517177.1:n.-291+80_-291+81delinsCT
XM_011518876.2:c.-4153+80_-4153+81delinsCT	XP_011517178.1:n.-4153+80_-4153+81delinsCT
XM_024447614.1:c.-321+80_-321+81delinsCT	XP_024303382.1:n.-321+80_-321+81delinsCT
XM_024447615.1:c.-321+80_-321+81delinsCT	XP_024303383.1:n.-321+80_-321+81delinsCT
NM_001271166.2:c.-321+80_-321+81delinsCT	NP_001258095.1:n.-321+80_-321+81delinsCT
NM_001271368.2:c.-291+80_-291+81delinsCT	NP_001258297.1:n.-291+80_-291+81delinsCT