Canonical Allele Identifier: CA1877491847

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371238C= , CM000671.2:g.122371238C=	GRCh38
NC_000009.11:g.125133517C= , CM000671.1:g.125133517C=	GRCh37
NC_000009.10:g.124173338C=	NCBI36
NG_032900.1:g.5289C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.60C= MANE Select	ENSP00000354612.2:p.Pro20=
ENST00000426608.6:c.60C=	ENSP00000411606.2:p.Pro20=
ENST00000540753.6:c.-238C=	ENSP00000437709.1:n.-238C=
ENST00000619306.5:c.60C=	ENSP00000483540.2:p.Pro20=
ENST00000643576.1:n.154C=
ENST00000643810.1:c.-268C=	ENSP00000494717.1:n.-268C=
ENST00000645132.1:n.227C=
ENST00000647067.1:c.60C=	ENSP00000495728.1:p.Pro20=
ENST00000223423.8:c.60C=	ENSP00000223423.4:p.Pro20=
ENST00000362012.6:c.60C=	ENSP00000354612.2:p.Pro20=
ENST00000426608.5:c.51C=	ENSP00000411606.1:p.Pro17=
ENST00000540753.5:c.-238C=	ENSP00000437709.1:n.-238C=
ENST00000614910.4:c.60C=	ENSP00000484800.1:p.Pro20=
ENST00000619306.4:c.153C=	ENSP00000483540.1:p.Pro51=
NM_000962.3:c.60C=	NP_000953.2:p.Pro20=
NM_001271164.1:c.60C=	NP_001258093.1:p.Pro20=
NM_001271166.1:c.-268C=	NP_001258095.1:n.-268C=
NM_001271367.1:c.-239C=	NP_001258296.1:n.-239C=
NM_001271368.1:c.-238C=	NP_001258297.1:n.-238C=
NM_080591.2:c.60C=	NP_542158.1:p.Pro20=
XM_005252105.2:c.-238C=	XP_005252162.1:n.-238C=
XM_011518875.1:c.-238C=	XP_011517177.1:n.-238C=
XM_011518876.1:c.-4100C=	XP_011517178.1:n.-4100C=
XM_005252105.3:c.-238C=	XP_005252162.1:n.-238C=
XM_011518875.2:c.-238C=	XP_011517177.1:n.-238C=
XM_011518876.2:c.-4100C=	XP_011517178.1:n.-4100C=
XM_024447614.1:c.-268C=	XP_024303382.1:n.-268C=
XM_024447615.1:c.-268C=	XP_024303383.1:n.-268C=
NM_000962.4:c.60C= MANE Select	NP_000953.2:p.Pro20=
NM_001271164.2:c.60C=	NP_001258093.1:p.Pro20=
NM_001271166.2:c.-268C=	NP_001258095.1:n.-268C=
NM_001271367.2:c.-239C=	NP_001258296.1:n.-239C=
NM_001271368.2:c.-238C=	NP_001258297.1:n.-238C=
NM_080591.3:c.60C=	NP_542158.1:p.Pro20=