Canonical Allele Identifier: CA374780677

Gene: PTGS1

Linked Data

• dbSNP Id: rs1291264280
• gnomAD v2: 9-125143725-A-G
• gnomAD v4: 9-122381446-A-G
• MyVariant Identifiers: chr9:g.125143725A>G (hg19) ; chr9:g.122381446A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381446A>G , CM000671.2:g.122381446A>G	GRCh38
NC_000009.11:g.125143725A>G , CM000671.1:g.125143725A>G	GRCh37
NC_000009.10:g.124183546A>G	NCBI36
NG_032900.1:g.15497A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.572A>G MANE Select	ENSP00000354612.2:p.Gln191Arg
ENST00000373698.7:c.245A>G	ENSP00000362802.5:p.Gln82Arg
ENST00000426608.6:c.313-50A>G	ENSP00000411606.2:n.313-50A>G
ENST00000540753.6:c.497A>G	ENSP00000437709.1:p.Gln166Arg
ENST00000619306.5:c.428A>G	ENSP00000483540.2:p.Gln143Arg
ENST00000643576.1:n.666A>G
ENST00000643810.1:c.245A>G	ENSP00000494717.1:p.Gln82Arg
ENST00000645132.1:n.519+2873A>G
ENST00000647067.1:c.*417A>G	ENSP00000495728.1:n.*417A>G
ENST00000223423.8:c.572A>G	ENSP00000223423.4:p.Gln191Arg
ENST00000362012.6:c.572A>G	ENSP00000354612.2:p.Gln191Arg
ENST00000373698.6:c.245A>G	ENSP00000362802.5:p.Gln82Arg
ENST00000426608.5:c.304-50A>G	ENSP00000411606.1:n.304-50A>G
ENST00000540753.5:c.497A>G	ENSP00000437709.1:p.Gln166Arg
ENST00000614910.4:c.428A>G	ENSP00000484800.1:p.Gln143Arg
ENST00000619306.4:c.665A>G	ENSP00000483540.1:p.Gln222Arg
NM_000962.3:c.572A>G	NP_000953.2:p.Gln191Arg
NM_001271164.1:c.428A>G	NP_001258093.1:p.Gln143Arg
NM_001271165.1:c.245A>G	NP_001258094.1:p.Gln82Arg
NM_001271166.1:c.245A>G	NP_001258095.1:p.Gln82Arg
NM_001271367.1:c.245A>G	NP_001258296.1:p.Gln82Arg
NM_001271368.1:c.497A>G	NP_001258297.1:p.Gln166Arg
NM_080591.2:c.572A>G	NP_542158.1:p.Gln191Arg
XM_005252105.2:c.497A>G	XP_005252162.1:p.Gln166Arg
XM_011518875.1:c.497A>G	XP_011517177.1:p.Gln166Arg
XM_011518876.1:c.245A>G	XP_011517178.1:p.Gln82Arg
XM_005252105.3:c.497A>G	XP_005252162.1:p.Gln166Arg
XM_011518875.2:c.497A>G	XP_011517177.1:p.Gln166Arg
XM_011518876.2:c.245A>G	XP_011517178.1:p.Gln82Arg
XM_024447614.1:c.245A>G	XP_024303382.1:p.Gln82Arg
XM_024447615.1:c.245A>G	XP_024303383.1:p.Gln82Arg
NM_000962.4:c.572A>G MANE Select	NP_000953.2:p.Gln191Arg
NM_001271164.2:c.428A>G	NP_001258093.1:p.Gln143Arg
NM_001271165.2:c.245A>G	NP_001258094.1:p.Gln82Arg
NM_001271166.2:c.245A>G	NP_001258095.1:p.Gln82Arg
NM_001271367.2:c.245A>G	NP_001258296.1:p.Gln82Arg
NM_001271368.2:c.497A>G	NP_001258297.1:p.Gln166Arg
NM_080591.3:c.572A>G	NP_542158.1:p.Gln191Arg