Canonical Allele Identifier: CA1877490434

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371058T= , CM000671.2:g.122371058T=	GRCh38
NC_000009.11:g.125133337T= , CM000671.1:g.125133337T=	GRCh37
NC_000009.10:g.124173158T=	NCBI36
NG_032900.1:g.5109T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.-27T= MANE Select	ENSP00000354612.2:n.-27T=
ENST00000540753.6:c.-290-128T=	ENSP00000437709.1:n.-290-128T=
ENST00000619306.5:c.-27T=	ENSP00000483540.2:n.-27T=
ENST00000643810.1:c.-320-128T=	ENSP00000494717.1:n.-320-128T=
ENST00000645132.1:n.47T=
ENST00000647067.1:c.-27T=	ENSP00000495728.1:n.-27T=
ENST00000540753.5:c.-290-128T=	ENSP00000437709.1:n.-290-128T=
ENST00000614910.4:c.-27T=	ENSP00000484800.1:n.-27T=
NM_000962.3:c.-27T=	NP_000953.2:n.-27T=
NM_001271164.1:c.-27T=	NP_001258093.1:n.-27T=
NM_001271166.1:c.-320-128T=	NP_001258095.1:n.-320-128T=
NM_001271367.1:c.-325T=	NP_001258296.1:n.-325T=
NM_001271368.1:c.-290-128T=	NP_001258297.1:n.-290-128T=
NM_080591.2:c.-27T=	NP_542158.1:n.-27T=
XM_005252105.2:c.-324T=	XP_005252162.1:n.-324T=
XM_011518875.1:c.-290-128T=	XP_011517177.1:n.-290-128T=
XM_011518876.1:c.-4152-128T=	XP_011517178.1:n.-4152-128T=
XM_005252105.3:c.-324T=	XP_005252162.1:n.-324T=
XM_011518875.2:c.-290-128T=	XP_011517177.1:n.-290-128T=
XM_011518876.2:c.-4152-128T=	XP_011517178.1:n.-4152-128T=
XM_024447614.1:c.-320-128T=	XP_024303382.1:n.-320-128T=
XM_024447615.1:c.-320-128T=	XP_024303383.1:n.-320-128T=
NM_000962.4:c.-27T= MANE Select	NP_000953.2:n.-27T=
NM_001271164.2:c.-27T=	NP_001258093.1:n.-27T=
NM_001271166.2:c.-320-128T=	NP_001258095.1:n.-320-128T=
NM_001271367.2:c.-325T=	NP_001258296.1:n.-325T=
NM_001271368.2:c.-290-128T=	NP_001258297.1:n.-290-128T=
NM_080591.3:c.-27T=	NP_542158.1:n.-27T=