Canonical Allele Identifier: CA13075038

Gene: PTGS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122374605A>G , CM000671.2:g.122374605A>G	GRCh38
NC_000009.11:g.125136884A>G , CM000671.1:g.125136884A>G	GRCh37
NC_000009.10:g.124176705A>G	NCBI36
NG_032900.1:g.8656A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.95-3294A>G MANE Select	ENSP00000354612.2:n.95-3294A>G
ENST00000426608.6:c.94+3333A>G	ENSP00000411606.2:n.94+3333A>G
ENST00000540753.6:c.19+2771A>G	ENSP00000437709.1:n.19+2771A>G
ENST00000619306.5:c.95-3294A>G	ENSP00000483540.2:n.95-3294A>G
ENST00000643576.1:n.189-3294A>G
ENST00000643810.1:c.-233-3294A>G	ENSP00000494717.1:n.-233-3294A>G
ENST00000645132.1:n.262-3294A>G
ENST00000647067.1:c.95-3323A>G	ENSP00000495728.1:n.95-3323A>G
ENST00000223423.8:c.95-3294A>G	ENSP00000223423.4:n.95-3294A>G
ENST00000362012.6:c.95-3294A>G	ENSP00000354612.2:n.95-3294A>G
ENST00000426608.5:c.85+3333A>G	ENSP00000411606.1:n.85+3333A>G
ENST00000540753.5:c.19+2771A>G	ENSP00000437709.1:n.19+2771A>G
ENST00000614910.4:c.95-3294A>G	ENSP00000484800.1:n.95-3294A>G
ENST00000619306.4:c.188-3294A>G	ENSP00000483540.1:n.188-3294A>G
NM_000962.3:c.95-3294A>G	NP_000953.2:n.95-3294A>G
NM_001271164.1:c.95-3294A>G	NP_001258093.1:n.95-3294A>G
NM_001271166.1:c.-233-3294A>G	NP_001258095.1:n.-233-3294A>G
NM_001271367.1:c.-204-3323A>G	NP_001258296.1:n.-204-3323A>G
NM_001271368.1:c.19+2771A>G	NP_001258297.1:n.19+2771A>G
NM_080591.2:c.95-3294A>G	NP_542158.1:n.95-3294A>G
XM_005252105.2:c.19+2771A>G	XP_005252162.1:n.19+2771A>G
XM_011518875.1:c.19+2771A>G	XP_011517177.1:n.19+2771A>G
XM_011518876.1:c.-1073A>G	XP_011517178.1:n.-1073A>G
XM_005252105.3:c.19+2771A>G	XP_005252162.1:n.19+2771A>G
XM_011518875.2:c.19+2771A>G	XP_011517177.1:n.19+2771A>G
XM_011518876.2:c.-1073A>G	XP_011517178.1:n.-1073A>G
XM_024447614.1:c.-233-3294A>G	XP_024303382.1:n.-233-3294A>G
XM_024447615.1:c.-233-3294A>G	XP_024303383.1:n.-233-3294A>G
NM_000962.4:c.95-3294A>G MANE Select	NP_000953.2:n.95-3294A>G
NM_001271164.2:c.95-3294A>G	NP_001258093.1:n.95-3294A>G
NM_001271166.2:c.-233-3294A>G	NP_001258095.1:n.-233-3294A>G
NM_001271367.2:c.-204-3323A>G	NP_001258296.1:n.-204-3323A>G
NM_001271368.2:c.19+2771A>G	NP_001258297.1:n.19+2771A>G
NM_080591.3:c.95-3294A>G	NP_542158.1:n.95-3294A>G