Canonical Allele Identifier: CA1128879598

Gene: PTGS1

Linked Data

• gnomAD v3: 9-122370972-C-CGGGGGGGGGGGG
• gnomAD v4: 9-122370972-C-CGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370977_122370978insGGGGGGGGGGGG , CM000671.2:g.122370977_122370978insGGGGGGGGGGGG	GRCh38
NC_000009.11:g.125133256_125133257insGGGGGGGGGGGG , CM000671.1:g.125133256_125133257insGGGGGGGGGGGG	GRCh37
NC_000009.10:g.124173077_124173078insGGGGGGGGGGGG	NCBI36
NG_032900.1:g.5028_5029insGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+135_-291+136insGGGGGGGGGGGG	ENSP00000437709.1:n.-291+135_-291+136insGGGGGGGGGGGG
ENST00000643810.1:c.-321+135_-321+136insGGGGGGGGGGGG	ENSP00000494717.1:n.-321+135_-321+136insGGGGGGGGGGGG
ENST00000540753.5:c.-291+135_-291+136insGGGGGGGGGGGG	ENSP00000437709.1:n.-291+135_-291+136insGGGGGGGGGGGG
NM_001271166.1:c.-321+135_-321+136insGGGGGGGGGGGG	NP_001258095.1:n.-321+135_-321+136insGGGGGGGGGGGG
NM_001271368.1:c.-291+135_-291+136insGGGGGGGGGGGG	NP_001258297.1:n.-291+135_-291+136insGGGGGGGGGGGG
XM_011518875.1:c.-291+135_-291+136insGGGGGGGGGGGG	XP_011517177.1:n.-291+135_-291+136insGGGGGGGGGGGG
XM_011518876.1:c.-4153+135_-4153+136insGGGGGGGGGGGG	XP_011517178.1:n.-4153+135_-4153+136insGGGGGGGGGGGG
XM_011518875.2:c.-291+135_-291+136insGGGGGGGGGGGG	XP_011517177.1:n.-291+135_-291+136insGGGGGGGGGGGG
XM_011518876.2:c.-4153+135_-4153+136insGGGGGGGGGGGG	XP_011517178.1:n.-4153+135_-4153+136insGGGGGGGGGGGG
XM_024447614.1:c.-321+135_-321+136insGGGGGGGGGGGG	XP_024303382.1:n.-321+135_-321+136insGGGGGGGGGGGG
XM_024447615.1:c.-321+135_-321+136insGGGGGGGGGGGG	XP_024303383.1:n.-321+135_-321+136insGGGGGGGGGGGG
NM_001271166.2:c.-321+135_-321+136insGGGGGGGGGGGG	NP_001258095.1:n.-321+135_-321+136insGGGGGGGGGGGG
NM_001271368.2:c.-291+135_-291+136insGGGGGGGGGGGG	NP_001258297.1:n.-291+135_-291+136insGGGGGGGGGGGG