Canonical Allele Identifier: CA199478816

Gene: PTGS1

Linked Data

• dbSNP Id: rs202141502
• gnomAD v4: 9-122381456-C-T
• MyVariant Identifiers: chr9:g.125143735C>T (hg19) ; chr9:g.122381456C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381456C>T , CM000671.2:g.122381456C>T	GRCh38
NC_000009.11:g.125143735C>T , CM000671.1:g.125143735C>T	GRCh37
NC_000009.10:g.124183556C>T	NCBI36
NG_032900.1:g.15507C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.582C>T MANE Select	ENSP00000354612.2:p.Asn194=
ENST00000373698.7:c.255C>T	ENSP00000362802.5:p.Asn85=
ENST00000426608.6:c.313-40C>T	ENSP00000411606.2:n.313-40C>T
ENST00000540753.6:c.507C>T	ENSP00000437709.1:p.Asn169=
ENST00000619306.5:c.438C>T	ENSP00000483540.2:p.Asn146=
ENST00000643576.1:n.676C>T
ENST00000643810.1:c.255C>T	ENSP00000494717.1:p.Asn85=
ENST00000645132.1:n.519+2883C>T
ENST00000647067.1:c.*427C>T	ENSP00000495728.1:n.*427C>T
ENST00000223423.8:c.582C>T	ENSP00000223423.4:p.Asn194=
ENST00000362012.6:c.582C>T	ENSP00000354612.2:p.Asn194=
ENST00000373698.6:c.255C>T	ENSP00000362802.5:p.Asn85=
ENST00000426608.5:c.304-40C>T	ENSP00000411606.1:n.304-40C>T
ENST00000540753.5:c.507C>T	ENSP00000437709.1:p.Asn169=
ENST00000614910.4:c.438C>T	ENSP00000484800.1:p.Asn146=
ENST00000619306.4:c.675C>T	ENSP00000483540.1:p.Asn225=
NM_000962.3:c.582C>T	NP_000953.2:p.Asn194=
NM_001271164.1:c.438C>T	NP_001258093.1:p.Asn146=
NM_001271165.1:c.255C>T	NP_001258094.1:p.Asn85=
NM_001271166.1:c.255C>T	NP_001258095.1:p.Asn85=
NM_001271367.1:c.255C>T	NP_001258296.1:p.Asn85=
NM_001271368.1:c.507C>T	NP_001258297.1:p.Asn169=
NM_080591.2:c.582C>T	NP_542158.1:p.Asn194=
XM_005252105.2:c.507C>T	XP_005252162.1:p.Asn169=
XM_011518875.1:c.507C>T	XP_011517177.1:p.Asn169=
XM_011518876.1:c.255C>T	XP_011517178.1:p.Asn85=
XM_005252105.3:c.507C>T	XP_005252162.1:p.Asn169=
XM_011518875.2:c.507C>T	XP_011517177.1:p.Asn169=
XM_011518876.2:c.255C>T	XP_011517178.1:p.Asn85=
XM_024447614.1:c.255C>T	XP_024303382.1:p.Asn85=
XM_024447615.1:c.255C>T	XP_024303383.1:p.Asn85=
NM_000962.4:c.582C>T MANE Select	NP_000953.2:p.Asn194=
NM_001271164.2:c.438C>T	NP_001258093.1:p.Asn146=
NM_001271165.2:c.255C>T	NP_001258094.1:p.Asn85=
NM_001271166.2:c.255C>T	NP_001258095.1:p.Asn85=
NM_001271367.2:c.255C>T	NP_001258296.1:p.Asn85=
NM_001271368.2:c.507C>T	NP_001258297.1:p.Asn169=
NM_080591.3:c.582C>T	NP_542158.1:p.Asn194=