Canonical Allele Identifier: CA590225512

Gene: PTGS1

Linked Data

• dbSNP Id: rs1182876781
• gnomAD v2: 9-125133261-GCC-G
• gnomAD v3: 9-122370982-GCC-G
• gnomAD v4: 9-122370982-GCC-G
• MyVariant Identifiers: chr9:g.125133262_125133263del (hg19) ; chr9:g.122370983_122370984del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370983_122370984del , CM000671.2:g.122370983_122370984del	GRCh38
NC_000009.11:g.125133262_125133263del , CM000671.1:g.125133262_125133263del	GRCh37
NC_000009.10:g.124173083_124173084del	NCBI36
NG_032900.1:g.5034_5035del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+141_-291+142del	ENSP00000437709.1:n.-291+141_-291+142del
ENST00000643810.1:c.-321+141_-321+142del	ENSP00000494717.1:n.-321+141_-321+142del
ENST00000540753.5:c.-291+141_-291+142del	ENSP00000437709.1:n.-291+141_-291+142del
NM_001271166.1:c.-321+141_-321+142del	NP_001258095.1:n.-321+141_-321+142del
NM_001271368.1:c.-291+141_-291+142del	NP_001258297.1:n.-291+141_-291+142del
XM_011518875.1:c.-291+141_-291+142del	XP_011517177.1:n.-291+141_-291+142del
XM_011518876.1:c.-4153+141_-4153+142del	XP_011517178.1:n.-4153+141_-4153+142del
XM_011518875.2:c.-291+141_-291+142del	XP_011517177.1:n.-291+141_-291+142del
XM_011518876.2:c.-4153+141_-4153+142del	XP_011517178.1:n.-4153+141_-4153+142del
XM_024447614.1:c.-321+141_-321+142del	XP_024303382.1:n.-321+141_-321+142del
XM_024447615.1:c.-321+141_-321+142del	XP_024303383.1:n.-321+141_-321+142del
NM_001271166.2:c.-321+141_-321+142del	NP_001258095.1:n.-321+141_-321+142del
NM_001271368.2:c.-291+141_-291+142del	NP_001258297.1:n.-291+141_-291+142del