Canonical Allele Identifier: CA1128879616

Gene: PTGS1

Linked Data

• gnomAD v3: 9-122370991-A-AGCGGGGGGAG
• gnomAD v4: 9-122370991-A-AGCGGGGGGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370992_122370993insCGGGGGGAGG , CM000671.2:g.122370992_122370993insCGGGGGGAGG	GRCh38
NC_000009.11:g.125133271_125133272insCGGGGGGAGG , CM000671.1:g.125133271_125133272insCGGGGGGAGG	GRCh37
NC_000009.10:g.124173092_124173093insCGGGGGGAGG	NCBI36
NG_032900.1:g.5043_5044insCGGGGGGAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+150_-291+151insCGGGGGGAGG	ENSP00000437709.1:n.-291+150_-291+151insCGGGGGGAGG
ENST00000643810.1:c.-321+150_-321+151insCGGGGGGAGG	ENSP00000494717.1:n.-321+150_-321+151insCGGGGGGAGG
ENST00000540753.5:c.-291+150_-291+151insCGGGGGGAGG	ENSP00000437709.1:n.-291+150_-291+151insCGGGGGGAGG
NM_001271166.1:c.-321+150_-321+151insCGGGGGGAGG	NP_001258095.1:n.-321+150_-321+151insCGGGGGGAGG
NM_001271368.1:c.-291+150_-291+151insCGGGGGGAGG	NP_001258297.1:n.-291+150_-291+151insCGGGGGGAGG
XM_011518875.1:c.-291+150_-291+151insCGGGGGGAGG	XP_011517177.1:n.-291+150_-291+151insCGGGGGGAGG
XM_011518876.1:c.-4153+150_-4153+151insCGGGGGGAGG	XP_011517178.1:n.-4153+150_-4153+151insCGGGGGGAGG
XM_011518875.2:c.-291+150_-291+151insCGGGGGGAGG	XP_011517177.1:n.-291+150_-291+151insCGGGGGGAGG
XM_011518876.2:c.-4153+150_-4153+151insCGGGGGGAGG	XP_011517178.1:n.-4153+150_-4153+151insCGGGGGGAGG
XM_024447614.1:c.-321+150_-321+151insCGGGGGGAGG	XP_024303382.1:n.-321+150_-321+151insCGGGGGGAGG
XM_024447615.1:c.-321+150_-321+151insCGGGGGGAGG	XP_024303383.1:n.-321+150_-321+151insCGGGGGGAGG
NM_001271166.2:c.-321+150_-321+151insCGGGGGGAGG	NP_001258095.1:n.-321+150_-321+151insCGGGGGGAGG
NM_001271368.2:c.-291+150_-291+151insCGGGGGGAGG	NP_001258297.1:n.-291+150_-291+151insCGGGGGGAGG