Canonical Allele Identifier: CA2579443202

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122371038-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371038A>G , CM000671.2:g.122371038A>G	GRCh38
NC_000009.11:g.125133317A>G , CM000671.1:g.125133317A>G	GRCh37
NC_000009.10:g.124173138A>G	NCBI36
NG_032900.1:g.5089A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.-47A>G MANE Select	ENSP00000354612.2:n.-47A>G
ENST00000540753.6:c.-290-148A>G	ENSP00000437709.1:n.-290-148A>G
ENST00000643810.1:c.-320-148A>G	ENSP00000494717.1:n.-320-148A>G
ENST00000645132.1:n.27A>G
ENST00000647067.1:c.-47A>G	ENSP00000495728.1:n.-47A>G
ENST00000540753.5:c.-290-148A>G	ENSP00000437709.1:n.-290-148A>G
ENST00000614910.4:c.-47A>G	ENSP00000484800.1:n.-47A>G
NM_000962.3:c.-47A>G	NP_000953.2:n.-47A>G
NM_001271164.1:c.-47A>G	NP_001258093.1:n.-47A>G
NM_001271166.1:c.-320-148A>G	NP_001258095.1:n.-320-148A>G
NM_001271367.1:c.-345A>G	NP_001258296.1:n.-345A>G
NM_001271368.1:c.-290-148A>G	NP_001258297.1:n.-290-148A>G
NM_080591.2:c.-47A>G	NP_542158.1:n.-47A>G
XM_011518875.1:c.-290-148A>G	XP_011517177.1:n.-290-148A>G
XM_011518876.1:c.-4152-148A>G	XP_011517178.1:n.-4152-148A>G
XM_011518875.2:c.-290-148A>G	XP_011517177.1:n.-290-148A>G
XM_011518876.2:c.-4152-148A>G	XP_011517178.1:n.-4152-148A>G
XM_024447614.1:c.-320-148A>G	XP_024303382.1:n.-320-148A>G
XM_024447615.1:c.-320-148A>G	XP_024303383.1:n.-320-148A>G
NM_000962.4:c.-47A>G MANE Select	NP_000953.2:n.-47A>G
NM_001271164.2:c.-47A>G	NP_001258093.1:n.-47A>G
NM_001271166.2:c.-320-148A>G	NP_001258095.1:n.-320-148A>G
NM_001271367.2:c.-345A>G	NP_001258296.1:n.-345A>G
NM_001271368.2:c.-290-148A>G	NP_001258297.1:n.-290-148A>G
NM_080591.3:c.-47A>G	NP_542158.1:n.-47A>G