Canonical Allele Identifier: CA374780772

Gene: PTGS1

Linked Data

• MyVariant Identifiers: chr9:g.125143742T>G (hg19) ; chr9:g.122381463T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381463T>G , CM000671.2:g.122381463T>G	GRCh38
NC_000009.11:g.125143742T>G , CM000671.1:g.125143742T>G	GRCh37
NC_000009.10:g.124183563T>G	NCBI36
NG_032900.1:g.15514T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.589T>G MANE Select	ENSP00000354612.2:p.Phe197Val
ENST00000373698.7:c.262T>G	ENSP00000362802.5:p.Phe88Val
ENST00000426608.6:c.313-33T>G	ENSP00000411606.2:n.313-33T>G
ENST00000540753.6:c.514T>G	ENSP00000437709.1:p.Phe172Val
ENST00000619306.5:c.445T>G	ENSP00000483540.2:p.Phe149Val
ENST00000643576.1:n.683T>G
ENST00000643810.1:c.262T>G	ENSP00000494717.1:p.Phe88Val
ENST00000645132.1:n.519+2890T>G
ENST00000647067.1:c.*434T>G	ENSP00000495728.1:n.*434T>G
ENST00000223423.8:c.589T>G	ENSP00000223423.4:p.Phe197Val
ENST00000362012.6:c.589T>G	ENSP00000354612.2:p.Phe197Val
ENST00000373698.6:c.262T>G	ENSP00000362802.5:p.Phe88Val
ENST00000426608.5:c.304-33T>G	ENSP00000411606.1:n.304-33T>G
ENST00000540753.5:c.514T>G	ENSP00000437709.1:p.Phe172Val
ENST00000614910.4:c.445T>G	ENSP00000484800.1:p.Phe149Val
ENST00000619306.4:c.682T>G	ENSP00000483540.1:p.Phe228Val
NM_000962.3:c.589T>G	NP_000953.2:p.Phe197Val
NM_001271164.1:c.445T>G	NP_001258093.1:p.Phe149Val
NM_001271165.1:c.262T>G	NP_001258094.1:p.Phe88Val
NM_001271166.1:c.262T>G	NP_001258095.1:p.Phe88Val
NM_001271367.1:c.262T>G	NP_001258296.1:p.Phe88Val
NM_001271368.1:c.514T>G	NP_001258297.1:p.Phe172Val
NM_080591.2:c.589T>G	NP_542158.1:p.Phe197Val
XM_005252105.2:c.514T>G	XP_005252162.1:p.Phe172Val
XM_011518875.1:c.514T>G	XP_011517177.1:p.Phe172Val
XM_011518876.1:c.262T>G	XP_011517178.1:p.Phe88Val
XM_005252105.3:c.514T>G	XP_005252162.1:p.Phe172Val
XM_011518875.2:c.514T>G	XP_011517177.1:p.Phe172Val
XM_011518876.2:c.262T>G	XP_011517178.1:p.Phe88Val
XM_024447614.1:c.262T>G	XP_024303382.1:p.Phe88Val
XM_024447615.1:c.262T>G	XP_024303383.1:p.Phe88Val
NM_000962.4:c.589T>G MANE Select	NP_000953.2:p.Phe197Val
NM_001271164.2:c.445T>G	NP_001258093.1:p.Phe149Val
NM_001271165.2:c.262T>G	NP_001258094.1:p.Phe88Val
NM_001271166.2:c.262T>G	NP_001258095.1:p.Phe88Val
NM_001271367.2:c.262T>G	NP_001258296.1:p.Phe88Val
NM_001271368.2:c.514T>G	NP_001258297.1:p.Phe172Val
NM_080591.3:c.589T>G	NP_542158.1:p.Phe197Val