Canonical Allele Identifier: CA466996541

Gene: PTGS1

Linked Data

• gnomAD v3: 9-122371000-A-AG
• gnomAD v4: 9-122371000-A-AG
• MyVariant Identifiers: chr9:g.125133279_125133280insG (hg19)

Genomic Alleles

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

Transcript Alleles

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