Canonical Allele Identifier: CA374780651

Gene: PTGS1

Linked Data

• MyVariant Identifiers: chr9:g.125143721C>G (hg19) ; chr9:g.122381442C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381442C>G , CM000671.2:g.122381442C>G	GRCh38
NC_000009.11:g.125143721C>G , CM000671.1:g.125143721C>G	GRCh37
NC_000009.10:g.124183542C>G	NCBI36
NG_032900.1:g.15493C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000362012.7:c.568C>G MANE Select	ENSP00000354612.2:p.Pro190Ala
ENST00000373698.7:c.241C>G	ENSP00000362802.5:p.Pro81Ala
ENST00000426608.6:c.313-54C>G	ENSP00000411606.2:n.313-54C>G
ENST00000540753.6:c.493C>G	ENSP00000437709.1:p.Pro165Ala
ENST00000619306.5:c.424C>G	ENSP00000483540.2:p.Pro142Ala
ENST00000643576.1:n.662C>G
ENST00000643810.1:c.241C>G	ENSP00000494717.1:p.Pro81Ala
ENST00000645132.1:n.519+2869C>G
ENST00000647067.1:c.*413C>G	ENSP00000495728.1:n.*413C>G
ENST00000223423.8:c.568C>G	ENSP00000223423.4:p.Pro190Ala
ENST00000362012.6:c.568C>G	ENSP00000354612.2:p.Pro190Ala
ENST00000373698.6:c.241C>G	ENSP00000362802.5:p.Pro81Ala
ENST00000426608.5:c.304-54C>G	ENSP00000411606.1:n.304-54C>G
ENST00000540753.5:c.493C>G	ENSP00000437709.1:p.Pro165Ala
ENST00000614910.4:c.424C>G	ENSP00000484800.1:p.Pro142Ala
ENST00000619306.4:c.661C>G	ENSP00000483540.1:p.Pro221Ala
NM_000962.3:c.568C>G	NP_000953.2:p.Pro190Ala
NM_001271164.1:c.424C>G	NP_001258093.1:p.Pro142Ala
NM_001271165.1:c.241C>G	NP_001258094.1:p.Pro81Ala
NM_001271166.1:c.241C>G	NP_001258095.1:p.Pro81Ala
NM_001271367.1:c.241C>G	NP_001258296.1:p.Pro81Ala
NM_001271368.1:c.493C>G	NP_001258297.1:p.Pro165Ala
NM_080591.2:c.568C>G	NP_542158.1:p.Pro190Ala
XM_005252105.2:c.493C>G	XP_005252162.1:p.Pro165Ala
XM_011518875.1:c.493C>G	XP_011517177.1:p.Pro165Ala
XM_011518876.1:c.241C>G	XP_011517178.1:p.Pro81Ala
XM_005252105.3:c.493C>G	XP_005252162.1:p.Pro165Ala
XM_011518875.2:c.493C>G	XP_011517177.1:p.Pro165Ala
XM_011518876.2:c.241C>G	XP_011517178.1:p.Pro81Ala
XM_024447614.1:c.241C>G	XP_024303382.1:p.Pro81Ala
XM_024447615.1:c.241C>G	XP_024303383.1:p.Pro81Ala
NM_000962.4:c.568C>G MANE Select	NP_000953.2:p.Pro190Ala
NM_001271164.2:c.424C>G	NP_001258093.1:p.Pro142Ala
NM_001271165.2:c.241C>G	NP_001258094.1:p.Pro81Ala
NM_001271166.2:c.241C>G	NP_001258095.1:p.Pro81Ala
NM_001271367.2:c.241C>G	NP_001258296.1:p.Pro81Ala
NM_001271368.2:c.493C>G	NP_001258297.1:p.Pro165Ala
NM_080591.3:c.568C>G	NP_542158.1:p.Pro190Ala