Canonical Allele Identifier: CA1877495008

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122377927G= , CM000671.2:g.122377927G=	GRCh38
NC_000009.11:g.125140206G= , CM000671.1:g.125140206G=	GRCh37
NC_000009.10:g.124180027G=	NCBI36
NG_032900.1:g.11978G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000962.4:c.123G= MANE Select	NP_000953.2:p.Gln41=
ENST00000362012.7:c.123G= MANE Select	ENSP00000354612.2:p.Gln41=
NM_000962.3:c.123G=	NP_000953.2:p.Gln41=
NM_001271164.1:c.123G=	NP_001258093.1:p.Gln41=
NM_001271164.2:c.123G=	NP_001258093.1:p.Gln41=
NM_001271165.1:c.-205G=	NP_001258094.1:n.-205G=
NM_001271165.2:c.-205G=	NP_001258094.1:n.-205G=
NM_001271166.1:c.-205G=	NP_001258095.1:n.-205G=
NM_001271166.2:c.-205G=	NP_001258095.1:n.-205G=
NM_001271367.1:c.-204-1G=	NP_001258296.1:n.-204-1G=
NM_001271367.2:c.-204-1G=	NP_001258296.1:n.-204-1G=
NM_001271368.1:c.48G=	NP_001258297.1:p.Gln16=
NM_001271368.2:c.48G=	NP_001258297.1:p.Gln16=
NM_080591.2:c.123G=	NP_542158.1:p.Gln41=
NM_080591.3:c.123G=	NP_542158.1:p.Gln41=
ENST00000223423.8:c.123G=	ENSP00000223423.4:p.Gln41=
ENST00000362012.6:c.123G=	ENSP00000354612.2:p.Gln41=
ENST00000373698.6:c.-205G=	ENSP00000362802.5:n.-205G=
ENST00000373698.7:c.-205G=	ENSP00000362802.5:n.-205G=
ENST00000426608.5:c.86-506G=	ENSP00000411606.1:n.86-506G=
ENST00000426608.6:c.95-506G=	ENSP00000411606.2:n.95-506G=
ENST00000540753.5:c.48G=	ENSP00000437709.1:p.Gln16=
ENST00000540753.6:c.48G=	ENSP00000437709.1:p.Gln16=
ENST00000614910.4:c.123G=	ENSP00000484800.1:p.Gln41=
ENST00000619306.4:c.216G=	ENSP00000483540.1:p.Gln72=
ENST00000619306.5:c.123G=	ENSP00000483540.2:p.Gln41=
ENST00000643576.1:n.217G=
ENST00000643810.1:c.-205G=	ENSP00000494717.1:n.-205G=
ENST00000645132.1:n.290G=
ENST00000647067.1:c.95-1G=	ENSP00000495728.1:n.95-1G=
XM_005252105.2:c.48G=	XP_005252162.1:p.Gln16=
XM_005252105.3:c.48G=	XP_005252162.1:p.Gln16=
XM_011518875.1:c.48G=	XP_011517177.1:p.Gln16=
XM_011518875.2:c.48G=	XP_011517177.1:p.Gln16=
XM_011518876.1:c.-205G=	XP_011517178.1:n.-205G=
XM_011518876.2:c.-205G=	XP_011517178.1:n.-205G=
XM_024447614.1:c.-205G=	XP_024303382.1:n.-205G=
XM_024447615.1:c.-205G=	XP_024303383.1:n.-205G=