Canonical Allele Identifier: CA467190911

Gene: PTGS1

Linked Data

• MyVariant Identifiers: chr9:g.125143687C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381408C>A , CM000671.2:g.122381408C>A	GRCh38
NC_000009.11:g.125143687C>A , CM000671.1:g.125143687C>A	GRCh37
NC_000009.10:g.124183508C>A	NCBI36
NG_032900.1:g.15459C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.534C>A MANE Select	ENSP00000354612.2:p.Arg178=
ENST00000373698.7:c.207C>A	ENSP00000362802.5:p.Arg69=
ENST00000426608.6:c.313-88C>A	ENSP00000411606.2:n.313-88C>A
ENST00000540753.6:c.459C>A	ENSP00000437709.1:p.Arg153=
ENST00000619306.5:c.390C>A	ENSP00000483540.2:p.Arg130=
ENST00000643576.1:n.628C>A
ENST00000643810.1:c.207C>A	ENSP00000494717.1:p.Arg69=
ENST00000645132.1:n.519+2835C>A
ENST00000647067.1:c.*379C>A	ENSP00000495728.1:n.*379C>A
ENST00000223423.8:c.534C>A	ENSP00000223423.4:p.Arg178=
ENST00000362012.6:c.534C>A	ENSP00000354612.2:p.Arg178=
ENST00000373698.6:c.207C>A	ENSP00000362802.5:p.Arg69=
ENST00000426608.5:c.304-88C>A	ENSP00000411606.1:n.304-88C>A
ENST00000540753.5:c.459C>A	ENSP00000437709.1:p.Arg153=
ENST00000614910.4:c.390C>A	ENSP00000484800.1:p.Arg130=
ENST00000619306.4:c.627C>A	ENSP00000483540.1:p.Arg209=
NM_000962.3:c.534C>A	NP_000953.2:p.Arg178=
NM_001271164.1:c.390C>A	NP_001258093.1:p.Arg130=
NM_001271165.1:c.207C>A	NP_001258094.1:p.Arg69=
NM_001271166.1:c.207C>A	NP_001258095.1:p.Arg69=
NM_001271367.1:c.207C>A	NP_001258296.1:p.Arg69=
NM_001271368.1:c.459C>A	NP_001258297.1:p.Arg153=
NM_080591.2:c.534C>A	NP_542158.1:p.Arg178=
XM_005252105.2:c.459C>A	XP_005252162.1:p.Arg153=
XM_011518875.1:c.459C>A	XP_011517177.1:p.Arg153=
XM_011518876.1:c.207C>A	XP_011517178.1:p.Arg69=
XM_005252105.3:c.459C>A	XP_005252162.1:p.Arg153=
XM_011518875.2:c.459C>A	XP_011517177.1:p.Arg153=
XM_011518876.2:c.207C>A	XP_011517178.1:p.Arg69=
XM_024447614.1:c.207C>A	XP_024303382.1:p.Arg69=
XM_024447615.1:c.207C>A	XP_024303383.1:p.Arg69=
NM_000962.4:c.534C>A MANE Select	NP_000953.2:p.Arg178=
NM_001271164.2:c.390C>A	NP_001258093.1:p.Arg130=
NM_001271165.2:c.207C>A	NP_001258094.1:p.Arg69=
NM_001271166.2:c.207C>A	NP_001258095.1:p.Arg69=
NM_001271367.2:c.207C>A	NP_001258296.1:p.Arg69=
NM_001271368.2:c.459C>A	NP_001258297.1:p.Arg153=
NM_080591.3:c.534C>A	NP_542158.1:p.Arg178=