Canonical Allele Identifier: CA374780627

Gene: PTGS1

Linked Data

• dbSNP Id: rs1342618257
• gnomAD v2: 9-125143716-C-G
• gnomAD v4: 9-122381437-C-G
• MyVariant Identifiers: chr9:g.125143716C>G (hg19) ; chr9:g.122381437C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381437C>G , CM000671.2:g.122381437C>G	GRCh38
NC_000009.11:g.125143716C>G , CM000671.1:g.125143716C>G	GRCh37
NC_000009.10:g.124183537C>G	NCBI36
NG_032900.1:g.15488C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000362012.7:c.563C>G MANE Select	ENSP00000354612.2:p.Pro188Arg
ENST00000373698.7:c.236C>G	ENSP00000362802.5:p.Pro79Arg
ENST00000426608.6:c.313-59C>G	ENSP00000411606.2:n.313-59C>G
ENST00000540753.6:c.488C>G	ENSP00000437709.1:p.Pro163Arg
ENST00000619306.5:c.419C>G	ENSP00000483540.2:p.Pro140Arg
ENST00000643576.1:n.657C>G
ENST00000643810.1:c.236C>G	ENSP00000494717.1:p.Pro79Arg
ENST00000645132.1:n.519+2864C>G
ENST00000647067.1:c.*408C>G	ENSP00000495728.1:n.*408C>G
ENST00000223423.8:c.563C>G	ENSP00000223423.4:p.Pro188Arg
ENST00000362012.6:c.563C>G	ENSP00000354612.2:p.Pro188Arg
ENST00000373698.6:c.236C>G	ENSP00000362802.5:p.Pro79Arg
ENST00000426608.5:c.304-59C>G	ENSP00000411606.1:n.304-59C>G
ENST00000540753.5:c.488C>G	ENSP00000437709.1:p.Pro163Arg
ENST00000614910.4:c.419C>G	ENSP00000484800.1:p.Pro140Arg
ENST00000619306.4:c.656C>G	ENSP00000483540.1:p.Pro219Arg
NM_000962.3:c.563C>G	NP_000953.2:p.Pro188Arg
NM_001271164.1:c.419C>G	NP_001258093.1:p.Pro140Arg
NM_001271165.1:c.236C>G	NP_001258094.1:p.Pro79Arg
NM_001271166.1:c.236C>G	NP_001258095.1:p.Pro79Arg
NM_001271367.1:c.236C>G	NP_001258296.1:p.Pro79Arg
NM_001271368.1:c.488C>G	NP_001258297.1:p.Pro163Arg
NM_080591.2:c.563C>G	NP_542158.1:p.Pro188Arg
XM_005252105.2:c.488C>G	XP_005252162.1:p.Pro163Arg
XM_011518875.1:c.488C>G	XP_011517177.1:p.Pro163Arg
XM_011518876.1:c.236C>G	XP_011517178.1:p.Pro79Arg
XM_005252105.3:c.488C>G	XP_005252162.1:p.Pro163Arg
XM_011518875.2:c.488C>G	XP_011517177.1:p.Pro163Arg
XM_011518876.2:c.236C>G	XP_011517178.1:p.Pro79Arg
XM_024447614.1:c.236C>G	XP_024303382.1:p.Pro79Arg
XM_024447615.1:c.236C>G	XP_024303383.1:p.Pro79Arg
NM_000962.4:c.563C>G MANE Select	NP_000953.2:p.Pro188Arg
NM_001271164.2:c.419C>G	NP_001258093.1:p.Pro140Arg
NM_001271165.2:c.236C>G	NP_001258094.1:p.Pro79Arg
NM_001271166.2:c.236C>G	NP_001258095.1:p.Pro79Arg
NM_001271367.2:c.236C>G	NP_001258296.1:p.Pro79Arg
NM_001271368.2:c.488C>G	NP_001258297.1:p.Pro163Arg
NM_080591.3:c.563C>G	NP_542158.1:p.Pro188Arg