Canonical Allele Identifier: CA1877495020

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122377962G= , CM000671.2:g.122377962G=	GRCh38
NC_000009.11:g.125140241G= , CM000671.1:g.125140241G=	GRCh37
NC_000009.10:g.124180062G=	NCBI36
NG_032900.1:g.12013G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000962.4:c.158G= MANE Select	NP_000953.2:p.Arg53=
ENST00000362012.7:c.158G= MANE Select	ENSP00000354612.2:p.Arg53=
NM_000962.3:c.158G=	NP_000953.2:p.Arg53=
NM_001271164.1:c.158G=	NP_001258093.1:p.Arg53=
NM_001271164.2:c.158G=	NP_001258093.1:p.Arg53=
NM_001271165.1:c.-170G=	NP_001258094.1:n.-170G=
NM_001271165.2:c.-170G=	NP_001258094.1:n.-170G=
NM_001271166.1:c.-170G=	NP_001258095.1:n.-170G=
NM_001271166.2:c.-170G=	NP_001258095.1:n.-170G=
NM_001271367.1:c.-170G=	NP_001258296.1:n.-170G=
NM_001271367.2:c.-170G=	NP_001258296.1:n.-170G=
NM_001271368.1:c.83G=	NP_001258297.1:p.Arg28=
NM_001271368.2:c.83G=	NP_001258297.1:p.Arg28=
NM_080591.2:c.158G=	NP_542158.1:p.Arg53=
NM_080591.3:c.158G=	NP_542158.1:p.Arg53=
ENST00000223423.8:c.158G=	ENSP00000223423.4:p.Arg53=
ENST00000362012.6:c.158G=	ENSP00000354612.2:p.Arg53=
ENST00000373698.6:c.-170G=	ENSP00000362802.5:n.-170G=
ENST00000373698.7:c.-170G=	ENSP00000362802.5:n.-170G=
ENST00000426608.5:c.86-471G=	ENSP00000411606.1:n.86-471G=
ENST00000426608.6:c.95-471G=	ENSP00000411606.2:n.95-471G=
ENST00000540753.5:c.83G=	ENSP00000437709.1:p.Arg28=
ENST00000540753.6:c.83G=	ENSP00000437709.1:p.Arg28=
ENST00000614910.4:c.158G=	ENSP00000484800.1:p.Arg53=
ENST00000619306.4:c.251G=	ENSP00000483540.1:p.Arg84=
ENST00000619306.5:c.158G=	ENSP00000483540.2:p.Arg53=
ENST00000643576.1:n.252G=
ENST00000643810.1:c.-170G=	ENSP00000494717.1:n.-170G=
ENST00000645132.1:n.325G=
ENST00000647067.1:c.*3G=	ENSP00000495728.1:n.*3G=
XM_005252105.2:c.83G=	XP_005252162.1:p.Arg28=
XM_005252105.3:c.83G=	XP_005252162.1:p.Arg28=
XM_011518875.1:c.83G=	XP_011517177.1:p.Arg28=
XM_011518875.2:c.83G=	XP_011517177.1:p.Arg28=
XM_011518876.1:c.-170G=	XP_011517178.1:n.-170G=
XM_011518876.2:c.-170G=	XP_011517178.1:n.-170G=
XM_024447614.1:c.-170G=	XP_024303382.1:n.-170G=
XM_024447615.1:c.-170G=	XP_024303383.1:n.-170G=