Canonical Allele Identifier: CA374780473

Gene: PTGS1

Linked Data

• dbSNP Id: rs745776199
• gnomAD v2: 9-125143685-C-A
• gnomAD v4: 9-122381406-C-A
• MyVariant Identifiers: chr9:g.125143685C>A (hg19) ; chr9:g.122381406C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381406C>A , CM000671.2:g.122381406C>A	GRCh38
NC_000009.11:g.125143685C>A , CM000671.1:g.125143685C>A	GRCh37
NC_000009.10:g.124183506C>A	NCBI36
NG_032900.1:g.15457C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.532C>A MANE Select	ENSP00000354612.2:p.Arg178Ser
ENST00000373698.7:c.205C>A	ENSP00000362802.5:p.Arg69Ser
ENST00000426608.6:c.313-90C>A	ENSP00000411606.2:n.313-90C>A
ENST00000540753.6:c.457C>A	ENSP00000437709.1:p.Arg153Ser
ENST00000619306.5:c.388C>A	ENSP00000483540.2:p.Arg130Ser
ENST00000643576.1:n.626C>A
ENST00000643810.1:c.205C>A	ENSP00000494717.1:p.Arg69Ser
ENST00000645132.1:n.519+2833C>A
ENST00000647067.1:c.*377C>A	ENSP00000495728.1:n.*377C>A
ENST00000223423.8:c.532C>A	ENSP00000223423.4:p.Arg178Ser
ENST00000362012.6:c.532C>A	ENSP00000354612.2:p.Arg178Ser
ENST00000373698.6:c.205C>A	ENSP00000362802.5:p.Arg69Ser
ENST00000426608.5:c.304-90C>A	ENSP00000411606.1:n.304-90C>A
ENST00000540753.5:c.457C>A	ENSP00000437709.1:p.Arg153Ser
ENST00000614910.4:c.388C>A	ENSP00000484800.1:p.Arg130Ser
ENST00000619306.4:c.625C>A	ENSP00000483540.1:p.Arg209Ser
NM_000962.3:c.532C>A	NP_000953.2:p.Arg178Ser
NM_001271164.1:c.388C>A	NP_001258093.1:p.Arg130Ser
NM_001271165.1:c.205C>A	NP_001258094.1:p.Arg69Ser
NM_001271166.1:c.205C>A	NP_001258095.1:p.Arg69Ser
NM_001271367.1:c.205C>A	NP_001258296.1:p.Arg69Ser
NM_001271368.1:c.457C>A	NP_001258297.1:p.Arg153Ser
NM_080591.2:c.532C>A	NP_542158.1:p.Arg178Ser
XM_005252105.2:c.457C>A	XP_005252162.1:p.Arg153Ser
XM_011518875.1:c.457C>A	XP_011517177.1:p.Arg153Ser
XM_011518876.1:c.205C>A	XP_011517178.1:p.Arg69Ser
XM_005252105.3:c.457C>A	XP_005252162.1:p.Arg153Ser
XM_011518875.2:c.457C>A	XP_011517177.1:p.Arg153Ser
XM_011518876.2:c.205C>A	XP_011517178.1:p.Arg69Ser
XM_024447614.1:c.205C>A	XP_024303382.1:p.Arg69Ser
XM_024447615.1:c.205C>A	XP_024303383.1:p.Arg69Ser
NM_000962.4:c.532C>A MANE Select	NP_000953.2:p.Arg178Ser
NM_001271164.2:c.388C>A	NP_001258093.1:p.Arg130Ser
NM_001271165.2:c.205C>A	NP_001258094.1:p.Arg69Ser
NM_001271166.2:c.205C>A	NP_001258095.1:p.Arg69Ser
NM_001271367.2:c.205C>A	NP_001258296.1:p.Arg69Ser
NM_001271368.2:c.457C>A	NP_001258297.1:p.Arg153Ser
NM_080591.3:c.532C>A	NP_542158.1:p.Arg178Ser