Canonical Allele Identifier: CA2691550139

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122370943-G-GCAGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370944_122370948dup , CM000671.2:g.122370944_122370948dup	GRCh38
NC_000009.11:g.125133223_125133227dup , CM000671.1:g.125133223_125133227dup	GRCh37
NC_000009.10:g.124173044_124173048dup	NCBI36
NG_032900.1:g.4995_4999dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+102_-291+106dup	ENSP00000437709.1:n.-291+102_-291+106dup
ENST00000643810.1:c.-321+102_-321+106dup	ENSP00000494717.1:n.-321+102_-321+106dup
ENST00000540753.5:c.-291+102_-291+106dup	ENSP00000437709.1:n.-291+102_-291+106dup
NM_001271166.1:c.-321+102_-321+106dup	NP_001258095.1:n.-321+102_-321+106dup
NM_001271368.1:c.-291+102_-291+106dup	NP_001258297.1:n.-291+102_-291+106dup
XM_011518875.1:c.-291+102_-291+106dup	XP_011517177.1:n.-291+102_-291+106dup
XM_011518876.1:c.-4153+102_-4153+106dup	XP_011517178.1:n.-4153+102_-4153+106dup
XM_011518875.2:c.-291+102_-291+106dup	XP_011517177.1:n.-291+102_-291+106dup
XM_011518876.2:c.-4153+102_-4153+106dup	XP_011517178.1:n.-4153+102_-4153+106dup
XM_024447614.1:c.-321+102_-321+106dup	XP_024303382.1:n.-321+102_-321+106dup
XM_024447615.1:c.-321+102_-321+106dup	XP_024303383.1:n.-321+102_-321+106dup
NM_001271166.2:c.-321+102_-321+106dup	NP_001258095.1:n.-321+102_-321+106dup
NM_001271368.2:c.-291+102_-291+106dup	NP_001258297.1:n.-291+102_-291+106dup