Canonical Allele Identifier: CA374780801

Gene: PTGS1

Linked Data

• COSMIC: COSM2154326
• MyVariant Identifiers: chr9:g.125143746C>T (hg19) ; chr9:g.122381467C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381467C>T , CM000671.2:g.122381467C>T	GRCh38
NC_000009.11:g.125143746C>T , CM000671.1:g.125143746C>T	GRCh37
NC_000009.10:g.124183567C>T	NCBI36
NG_032900.1:g.15518C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.593C>T MANE Select	ENSP00000354612.2:p.Ala198Val
ENST00000373698.7:c.266C>T	ENSP00000362802.5:p.Ala89Val
ENST00000426608.6:c.313-29C>T	ENSP00000411606.2:n.313-29C>T
ENST00000540753.6:c.518C>T	ENSP00000437709.1:p.Ala173Val
ENST00000619306.5:c.449C>T	ENSP00000483540.2:p.Ala150Val
ENST00000643576.1:n.687C>T
ENST00000643810.1:c.266C>T	ENSP00000494717.1:p.Ala89Val
ENST00000645132.1:n.519+2894C>T
ENST00000647067.1:c.*438C>T	ENSP00000495728.1:n.*438C>T
ENST00000223423.8:c.593C>T	ENSP00000223423.4:p.Ala198Val
ENST00000362012.6:c.593C>T	ENSP00000354612.2:p.Ala198Val
ENST00000373698.6:c.266C>T	ENSP00000362802.5:p.Ala89Val
ENST00000426608.5:c.304-29C>T	ENSP00000411606.1:n.304-29C>T
ENST00000540753.5:c.518C>T	ENSP00000437709.1:p.Ala173Val
ENST00000614910.4:c.449C>T	ENSP00000484800.1:p.Ala150Val
ENST00000619306.4:c.686C>T	ENSP00000483540.1:p.Ala229Val
NM_000962.3:c.593C>T	NP_000953.2:p.Ala198Val
NM_001271164.1:c.449C>T	NP_001258093.1:p.Ala150Val
NM_001271165.1:c.266C>T	NP_001258094.1:p.Ala89Val
NM_001271166.1:c.266C>T	NP_001258095.1:p.Ala89Val
NM_001271367.1:c.266C>T	NP_001258296.1:p.Ala89Val
NM_001271368.1:c.518C>T	NP_001258297.1:p.Ala173Val
NM_080591.2:c.593C>T	NP_542158.1:p.Ala198Val
XM_005252105.2:c.518C>T	XP_005252162.1:p.Ala173Val
XM_011518875.1:c.518C>T	XP_011517177.1:p.Ala173Val
XM_011518876.1:c.266C>T	XP_011517178.1:p.Ala89Val
XM_005252105.3:c.518C>T	XP_005252162.1:p.Ala173Val
XM_011518875.2:c.518C>T	XP_011517177.1:p.Ala173Val
XM_011518876.2:c.266C>T	XP_011517178.1:p.Ala89Val
XM_024447614.1:c.266C>T	XP_024303382.1:p.Ala89Val
XM_024447615.1:c.266C>T	XP_024303383.1:p.Ala89Val
NM_000962.4:c.593C>T MANE Select	NP_000953.2:p.Ala198Val
NM_001271164.2:c.449C>T	NP_001258093.1:p.Ala150Val
NM_001271165.2:c.266C>T	NP_001258094.1:p.Ala89Val
NM_001271166.2:c.266C>T	NP_001258095.1:p.Ala89Val
NM_001271367.2:c.266C>T	NP_001258296.1:p.Ala89Val
NM_001271368.2:c.518C>T	NP_001258297.1:p.Ala173Val
NM_080591.3:c.593C>T	NP_542158.1:p.Ala198Val