Canonical Allele Identifier: CA374780569

Gene: PTGS1

Linked Data

• MyVariant Identifiers: chr9:g.125143709T>G (hg19) ; chr9:g.122381430T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381430T>G , CM000671.2:g.122381430T>G	GRCh38
NC_000009.11:g.125143709T>G , CM000671.1:g.125143709T>G	GRCh37
NC_000009.10:g.124183530T>G	NCBI36
NG_032900.1:g.15481T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000362012.7:c.556T>G MANE Select	ENSP00000354612.2:p.Phe186Val
ENST00000373698.7:c.229T>G	ENSP00000362802.5:p.Phe77Val
ENST00000426608.6:c.313-66T>G	ENSP00000411606.2:n.313-66T>G
ENST00000540753.6:c.481T>G	ENSP00000437709.1:p.Phe161Val
ENST00000619306.5:c.412T>G	ENSP00000483540.2:p.Phe138Val
ENST00000643576.1:n.650T>G
ENST00000643810.1:c.229T>G	ENSP00000494717.1:p.Phe77Val
ENST00000645132.1:n.519+2857T>G
ENST00000647067.1:c.*401T>G	ENSP00000495728.1:n.*401T>G
ENST00000223423.8:c.556T>G	ENSP00000223423.4:p.Phe186Val
ENST00000362012.6:c.556T>G	ENSP00000354612.2:p.Phe186Val
ENST00000373698.6:c.229T>G	ENSP00000362802.5:p.Phe77Val
ENST00000426608.5:c.304-66T>G	ENSP00000411606.1:n.304-66T>G
ENST00000540753.5:c.481T>G	ENSP00000437709.1:p.Phe161Val
ENST00000614910.4:c.412T>G	ENSP00000484800.1:p.Phe138Val
ENST00000619306.4:c.649T>G	ENSP00000483540.1:p.Phe217Val
NM_000962.3:c.556T>G	NP_000953.2:p.Phe186Val
NM_001271164.1:c.412T>G	NP_001258093.1:p.Phe138Val
NM_001271165.1:c.229T>G	NP_001258094.1:p.Phe77Val
NM_001271166.1:c.229T>G	NP_001258095.1:p.Phe77Val
NM_001271367.1:c.229T>G	NP_001258296.1:p.Phe77Val
NM_001271368.1:c.481T>G	NP_001258297.1:p.Phe161Val
NM_080591.2:c.556T>G	NP_542158.1:p.Phe186Val
XM_005252105.2:c.481T>G	XP_005252162.1:p.Phe161Val
XM_011518875.1:c.481T>G	XP_011517177.1:p.Phe161Val
XM_011518876.1:c.229T>G	XP_011517178.1:p.Phe77Val
XM_005252105.3:c.481T>G	XP_005252162.1:p.Phe161Val
XM_011518875.2:c.481T>G	XP_011517177.1:p.Phe161Val
XM_011518876.2:c.229T>G	XP_011517178.1:p.Phe77Val
XM_024447614.1:c.229T>G	XP_024303382.1:p.Phe77Val
XM_024447615.1:c.229T>G	XP_024303383.1:p.Phe77Val
NM_000962.4:c.556T>G MANE Select	NP_000953.2:p.Phe186Val
NM_001271164.2:c.412T>G	NP_001258093.1:p.Phe138Val
NM_001271165.2:c.229T>G	NP_001258094.1:p.Phe77Val
NM_001271166.2:c.229T>G	NP_001258095.1:p.Phe77Val
NM_001271367.2:c.229T>G	NP_001258296.1:p.Phe77Val
NM_001271368.2:c.481T>G	NP_001258297.1:p.Phe161Val
NM_080591.3:c.556T>G	NP_542158.1:p.Phe186Val