Canonical Allele Identifier: CA1128879640

Gene: PTGS1

Linked Data

• gnomAD v3: 9-122370995-T-TGGGGAGGGGG
• gnomAD v4: 9-122370995-T-TGGGGAGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371004_122371005insGGGGGAGGGG , CM000671.2:g.122371004_122371005insGGGGGAGGGG	GRCh38
NC_000009.11:g.125133283_125133284insGGGGGAGGGG , CM000671.1:g.125133283_125133284insGGGGGAGGGG	GRCh37
NC_000009.10:g.124173104_124173105insGGGGGAGGGG	NCBI36
NG_032900.1:g.5055_5056insGGGGGAGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+162_-291+163insGGGGGAGGGG	ENSP00000437709.1:n.-291+162_-291+163insGGGGGAGGGG
ENST00000643810.1:c.-321+162_-321+163insGGGGGAGGGG	ENSP00000494717.1:n.-321+162_-321+163insGGGGGAGGGG
ENST00000540753.5:c.-291+162_-291+163insGGGGGAGGGG	ENSP00000437709.1:n.-291+162_-291+163insGGGGGAGGGG
NM_001271166.1:c.-321+162_-321+163insGGGGGAGGGG	NP_001258095.1:n.-321+162_-321+163insGGGGGAGGGG
NM_001271368.1:c.-291+162_-291+163insGGGGGAGGGG	NP_001258297.1:n.-291+162_-291+163insGGGGGAGGGG
XM_011518875.1:c.-291+162_-291+163insGGGGGAGGGG	XP_011517177.1:n.-291+162_-291+163insGGGGGAGGGG
XM_011518876.1:c.-4153+162_-4153+163insGGGGGAGGGG	XP_011517178.1:n.-4153+162_-4153+163insGGGGGAGGGG
XM_011518875.2:c.-291+162_-291+163insGGGGGAGGGG	XP_011517177.1:n.-291+162_-291+163insGGGGGAGGGG
XM_011518876.2:c.-4153+162_-4153+163insGGGGGAGGGG	XP_011517178.1:n.-4153+162_-4153+163insGGGGGAGGGG
XM_024447614.1:c.-321+162_-321+163insGGGGGAGGGG	XP_024303382.1:n.-321+162_-321+163insGGGGGAGGGG
XM_024447615.1:c.-321+162_-321+163insGGGGGAGGGG	XP_024303383.1:n.-321+162_-321+163insGGGGGAGGGG
NM_001271166.2:c.-321+162_-321+163insGGGGGAGGGG	NP_001258095.1:n.-321+162_-321+163insGGGGGAGGGG
NM_001271368.2:c.-291+162_-291+163insGGGGGAGGGG	NP_001258297.1:n.-291+162_-291+163insGGGGGAGGGG