Canonical Allele Identifier: CA2785849934

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122371018C>G , CM000671.2:g.122371018C>G	GRCh38
NC_000009.11:g.125133297C>G , CM000671.1:g.125133297C>G	GRCh37
NC_000009.10:g.124173118C>G	NCBI36
NG_032900.1:g.5069C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-290-168C>G	ENSP00000437709.1:n.-290-168C>G
ENST00000643810.1:c.-320-168C>G	ENSP00000494717.1:n.-320-168C>G
ENST00000645132.1:n.7C>G
ENST00000540753.5:c.-290-168C>G	ENSP00000437709.1:n.-290-168C>G
ENST00000614910.4:c.-67C>G	ENSP00000484800.1:n.-67C>G
NM_000962.3:c.-67C>G	NP_000953.2:n.-67C>G
NM_001271164.1:c.-67C>G	NP_001258093.1:n.-67C>G
NM_001271166.1:c.-320-168C>G	NP_001258095.1:n.-320-168C>G
NM_001271367.1:c.-365C>G	NP_001258296.1:n.-365C>G
NM_001271368.1:c.-290-168C>G	NP_001258297.1:n.-290-168C>G
NM_080591.2:c.-67C>G	NP_542158.1:n.-67C>G
XM_011518875.1:c.-290-168C>G	XP_011517177.1:n.-290-168C>G
XM_011518876.1:c.-4152-168C>G	XP_011517178.1:n.-4152-168C>G
XM_011518875.2:c.-290-168C>G	XP_011517177.1:n.-290-168C>G
XM_011518876.2:c.-4152-168C>G	XP_011517178.1:n.-4152-168C>G
XM_024447614.1:c.-320-168C>G	XP_024303382.1:n.-320-168C>G
XM_024447615.1:c.-320-168C>G	XP_024303383.1:n.-320-168C>G
NM_001271166.2:c.-320-168C>G	NP_001258095.1:n.-320-168C>G
NM_001271368.2:c.-290-168C>G	NP_001258297.1:n.-290-168C>G