Canonical Allele Identifier: CA1877492688

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122373123_122373124delinsGA , CM000671.2:g.122373123_122373124delinsGA	GRCh38
NC_000009.11:g.125135402_125135403delinsGA , CM000671.1:g.125135402_125135403delinsGA	GRCh37
NC_000009.10:g.124175223_124175224delinsGA	NCBI36
NG_032900.1:g.7174_7175delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.94+1851_94+1852delinsGA MANE Select	ENSP00000354612.2:n.94+1851_94+1852delinsGA
ENST00000426608.6:c.94+1851_94+1852delinsGA	ENSP00000411606.2:n.94+1851_94+1852delinsGA
ENST00000540753.6:c.19+1289_19+1290delinsGA	ENSP00000437709.1:n.19+1289_19+1290delinsGA
ENST00000619306.5:c.94+1851_94+1852delinsGA	ENSP00000483540.2:n.94+1851_94+1852delinsGA
ENST00000643576.1:n.188+1851_188+1852delinsGA
ENST00000643810.1:c.-234+1851_-234+1852delinsGA	ENSP00000494717.1:n.-234+1851_-234+1852delinsGA
ENST00000645132.1:n.261+1851_261+1852delinsGA
ENST00000647067.1:c.94+1851_94+1852delinsGA	ENSP00000495728.1:n.94+1851_94+1852delinsGA
ENST00000223423.8:c.94+1851_94+1852delinsGA	ENSP00000223423.4:n.94+1851_94+1852delinsGA
ENST00000362012.6:c.94+1851_94+1852delinsGA	ENSP00000354612.2:n.94+1851_94+1852delinsGA
ENST00000426608.5:c.85+1851_85+1852delinsGA	ENSP00000411606.1:n.85+1851_85+1852delinsGA
ENST00000540753.5:c.19+1289_19+1290delinsGA	ENSP00000437709.1:n.19+1289_19+1290delinsGA
ENST00000614910.4:c.94+1851_94+1852delinsGA	ENSP00000484800.1:n.94+1851_94+1852delinsGA
ENST00000619306.4:c.187+1851_187+1852delinsGA	ENSP00000483540.1:n.187+1851_187+1852delinsGA
NM_000962.3:c.94+1851_94+1852delinsGA	NP_000953.2:n.94+1851_94+1852delinsGA
NM_001271164.1:c.94+1851_94+1852delinsGA	NP_001258093.1:n.94+1851_94+1852delinsGA
NM_001271166.1:c.-234+1851_-234+1852delinsGA	NP_001258095.1:n.-234+1851_-234+1852delinsGA
NM_001271367.1:c.-205+1851_-205+1852delinsGA	NP_001258296.1:n.-205+1851_-205+1852delinsGA
NM_001271368.1:c.19+1289_19+1290delinsGA	NP_001258297.1:n.19+1289_19+1290delinsGA
NM_080591.2:c.94+1851_94+1852delinsGA	NP_542158.1:n.94+1851_94+1852delinsGA
XM_005252105.2:c.19+1289_19+1290delinsGA	XP_005252162.1:n.19+1289_19+1290delinsGA
XM_011518875.1:c.19+1289_19+1290delinsGA	XP_011517177.1:n.19+1289_19+1290delinsGA
XM_011518876.1:c.-2555_-2554delinsGA	XP_011517178.1:n.-2555_-2554delinsGA
XM_005252105.3:c.19+1289_19+1290delinsGA	XP_005252162.1:n.19+1289_19+1290delinsGA
XM_011518875.2:c.19+1289_19+1290delinsGA	XP_011517177.1:n.19+1289_19+1290delinsGA
XM_011518876.2:c.-2555_-2554delinsGA	XP_011517178.1:n.-2555_-2554delinsGA
XM_024447614.1:c.-234+1851_-234+1852delinsGA	XP_024303382.1:n.-234+1851_-234+1852delinsGA
XM_024447615.1:c.-234+1851_-234+1852delinsGA	XP_024303383.1:n.-234+1851_-234+1852delinsGA
NM_000962.4:c.94+1851_94+1852delinsGA MANE Select	NP_000953.2:n.94+1851_94+1852delinsGA
NM_001271164.2:c.94+1851_94+1852delinsGA	NP_001258093.1:n.94+1851_94+1852delinsGA
NM_001271166.2:c.-234+1851_-234+1852delinsGA	NP_001258095.1:n.-234+1851_-234+1852delinsGA
NM_001271367.2:c.-205+1851_-205+1852delinsGA	NP_001258296.1:n.-205+1851_-205+1852delinsGA
NM_001271368.2:c.19+1289_19+1290delinsGA	NP_001258297.1:n.19+1289_19+1290delinsGA
NM_080591.3:c.94+1851_94+1852delinsGA	NP_542158.1:n.94+1851_94+1852delinsGA