Canonical Allele Identifier: CA2691550192

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122370995-T-TTGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370995_122370996insTGGGGG , CM000671.2:g.122370995_122370996insTGGGGG	GRCh38
NC_000009.11:g.125133274_125133275insTGGGGG , CM000671.1:g.125133274_125133275insTGGGGG	GRCh37
NC_000009.10:g.124173095_124173096insTGGGGG	NCBI36
NG_032900.1:g.5046_5047insTGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+153_-291+154insTGGGGG	ENSP00000437709.1:n.-291+153_-291+154insTGGGGG
ENST00000643810.1:c.-321+153_-321+154insTGGGGG	ENSP00000494717.1:n.-321+153_-321+154insTGGGGG
ENST00000540753.5:c.-291+153_-291+154insTGGGGG	ENSP00000437709.1:n.-291+153_-291+154insTGGGGG
NM_001271166.1:c.-321+153_-321+154insTGGGGG	NP_001258095.1:n.-321+153_-321+154insTGGGGG
NM_001271368.1:c.-291+153_-291+154insTGGGGG	NP_001258297.1:n.-291+153_-291+154insTGGGGG
XM_011518875.1:c.-291+153_-291+154insTGGGGG	XP_011517177.1:n.-291+153_-291+154insTGGGGG
XM_011518876.1:c.-4153+153_-4153+154insTGGGGG	XP_011517178.1:n.-4153+153_-4153+154insTGGGGG
XM_011518875.2:c.-291+153_-291+154insTGGGGG	XP_011517177.1:n.-291+153_-291+154insTGGGGG
XM_011518876.2:c.-4153+153_-4153+154insTGGGGG	XP_011517178.1:n.-4153+153_-4153+154insTGGGGG
XM_024447614.1:c.-321+153_-321+154insTGGGGG	XP_024303382.1:n.-321+153_-321+154insTGGGGG
XM_024447615.1:c.-321+153_-321+154insTGGGGG	XP_024303383.1:n.-321+153_-321+154insTGGGGG
NM_001271166.2:c.-321+153_-321+154insTGGGGG	NP_001258095.1:n.-321+153_-321+154insTGGGGG
NM_001271368.2:c.-291+153_-291+154insTGGGGG	NP_001258297.1:n.-291+153_-291+154insTGGGGG