Canonical Allele Identifier: CA1877491849

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371240T= , CM000671.2:g.122371240T=	GRCh38
NC_000009.11:g.125133519T= , CM000671.1:g.125133519T=	GRCh37
NC_000009.10:g.124173340T=	NCBI36
NG_032900.1:g.5291T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.62T= MANE Select	ENSP00000354612.2:p.Val21=
ENST00000426608.6:c.62T=	ENSP00000411606.2:p.Val21=
ENST00000540753.6:c.-236T=	ENSP00000437709.1:n.-236T=
ENST00000619306.5:c.62T=	ENSP00000483540.2:p.Val21=
ENST00000643576.1:n.156T=
ENST00000643810.1:c.-266T=	ENSP00000494717.1:n.-266T=
ENST00000645132.1:n.229T=
ENST00000647067.1:c.62T=	ENSP00000495728.1:p.Val21=
ENST00000223423.8:c.62T=	ENSP00000223423.4:p.Val21=
ENST00000362012.6:c.62T=	ENSP00000354612.2:p.Val21=
ENST00000426608.5:c.53T=	ENSP00000411606.1:p.Val18=
ENST00000540753.5:c.-236T=	ENSP00000437709.1:n.-236T=
ENST00000614910.4:c.62T=	ENSP00000484800.1:p.Val21=
ENST00000619306.4:c.155T=	ENSP00000483540.1:p.Val52=
NM_000962.3:c.62T=	NP_000953.2:p.Val21=
NM_001271164.1:c.62T=	NP_001258093.1:p.Val21=
NM_001271166.1:c.-266T=	NP_001258095.1:n.-266T=
NM_001271367.1:c.-237T=	NP_001258296.1:n.-237T=
NM_001271368.1:c.-236T=	NP_001258297.1:n.-236T=
NM_080591.2:c.62T=	NP_542158.1:p.Val21=
XM_005252105.2:c.-236T=	XP_005252162.1:n.-236T=
XM_011518875.1:c.-236T=	XP_011517177.1:n.-236T=
XM_011518876.1:c.-4098T=	XP_011517178.1:n.-4098T=
XM_005252105.3:c.-236T=	XP_005252162.1:n.-236T=
XM_011518875.2:c.-236T=	XP_011517177.1:n.-236T=
XM_011518876.2:c.-4098T=	XP_011517178.1:n.-4098T=
XM_024447614.1:c.-266T=	XP_024303382.1:n.-266T=
XM_024447615.1:c.-266T=	XP_024303383.1:n.-266T=
NM_000962.4:c.62T= MANE Select	NP_000953.2:p.Val21=
NM_001271164.2:c.62T=	NP_001258093.1:p.Val21=
NM_001271166.2:c.-266T=	NP_001258095.1:n.-266T=
NM_001271367.2:c.-237T=	NP_001258296.1:n.-237T=
NM_001271368.2:c.-236T=	NP_001258297.1:n.-236T=
NM_080591.3:c.62T=	NP_542158.1:p.Val21=