Canonical Allele Identifier: CA467190950

Gene: PTGS1

Linked Data

• COSMIC: COSM2154324
• MyVariant Identifiers: chr9:g.125143747C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381468C>G , CM000671.2:g.122381468C>G	GRCh38
NC_000009.11:g.125143747C>G , CM000671.1:g.125143747C>G	GRCh37
NC_000009.10:g.124183568C>G	NCBI36
NG_032900.1:g.15519C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.594C>G MANE Select	ENSP00000354612.2:p.Ala198=
ENST00000373698.7:c.267C>G	ENSP00000362802.5:p.Ala89=
ENST00000426608.6:c.313-28C>G	ENSP00000411606.2:n.313-28C>G
ENST00000540753.6:c.519C>G	ENSP00000437709.1:p.Ala173=
ENST00000619306.5:c.450C>G	ENSP00000483540.2:p.Ala150=
ENST00000643576.1:n.688C>G
ENST00000643810.1:c.267C>G	ENSP00000494717.1:p.Ala89=
ENST00000645132.1:n.519+2895C>G
ENST00000647067.1:c.*439C>G	ENSP00000495728.1:n.*439C>G
ENST00000223423.8:c.594C>G	ENSP00000223423.4:p.Ala198=
ENST00000362012.6:c.594C>G	ENSP00000354612.2:p.Ala198=
ENST00000373698.6:c.267C>G	ENSP00000362802.5:p.Ala89=
ENST00000426608.5:c.304-28C>G	ENSP00000411606.1:n.304-28C>G
ENST00000540753.5:c.519C>G	ENSP00000437709.1:p.Ala173=
ENST00000614910.4:c.450C>G	ENSP00000484800.1:p.Ala150=
ENST00000619306.4:c.687C>G	ENSP00000483540.1:p.Ala229=
NM_000962.3:c.594C>G	NP_000953.2:p.Ala198=
NM_001271164.1:c.450C>G	NP_001258093.1:p.Ala150=
NM_001271165.1:c.267C>G	NP_001258094.1:p.Ala89=
NM_001271166.1:c.267C>G	NP_001258095.1:p.Ala89=
NM_001271367.1:c.267C>G	NP_001258296.1:p.Ala89=
NM_001271368.1:c.519C>G	NP_001258297.1:p.Ala173=
NM_080591.2:c.594C>G	NP_542158.1:p.Ala198=
XM_005252105.2:c.519C>G	XP_005252162.1:p.Ala173=
XM_011518875.1:c.519C>G	XP_011517177.1:p.Ala173=
XM_011518876.1:c.267C>G	XP_011517178.1:p.Ala89=
XM_005252105.3:c.519C>G	XP_005252162.1:p.Ala173=
XM_011518875.2:c.519C>G	XP_011517177.1:p.Ala173=
XM_011518876.2:c.267C>G	XP_011517178.1:p.Ala89=
XM_024447614.1:c.267C>G	XP_024303382.1:p.Ala89=
XM_024447615.1:c.267C>G	XP_024303383.1:p.Ala89=
NM_000962.4:c.594C>G MANE Select	NP_000953.2:p.Ala198=
NM_001271164.2:c.450C>G	NP_001258093.1:p.Ala150=
NM_001271165.2:c.267C>G	NP_001258094.1:p.Ala89=
NM_001271166.2:c.267C>G	NP_001258095.1:p.Ala89=
NM_001271367.2:c.267C>G	NP_001258296.1:p.Ala89=
NM_001271368.2:c.519C>G	NP_001258297.1:p.Ala173=
NM_080591.3:c.594C>G	NP_542158.1:p.Ala198=