Canonical Allele Identifier: CA374780915

Gene: PTGS1

Linked Data

• MyVariant Identifiers: chr9:g.125143770A>C (hg19) ; chr9:g.122381491A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381491A>C , CM000671.2:g.122381491A>C	GRCh38
NC_000009.11:g.125143770A>C , CM000671.1:g.125143770A>C	GRCh37
NC_000009.10:g.124183591A>C	NCBI36
NG_032900.1:g.15542A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.617A>C MANE Select	ENSP00000354612.2:p.His206Pro
ENST00000373698.7:c.290A>C	ENSP00000362802.5:p.His97Pro
ENST00000426608.6:c.313-5A>C	ENSP00000411606.2:n.313-5A>C
ENST00000540753.6:c.542A>C	ENSP00000437709.1:p.His181Pro
ENST00000619306.5:c.473A>C	ENSP00000483540.2:p.His158Pro
ENST00000643576.1:n.711A>C
ENST00000643810.1:c.290A>C	ENSP00000494717.1:p.His97Pro
ENST00000645132.1:n.519+2918A>C
ENST00000647067.1:c.*462A>C	ENSP00000495728.1:n.*462A>C
ENST00000223423.8:c.617A>C	ENSP00000223423.4:p.His206Pro
ENST00000362012.6:c.617A>C	ENSP00000354612.2:p.His206Pro
ENST00000373698.6:c.290A>C	ENSP00000362802.5:p.His97Pro
ENST00000426608.5:c.304-5A>C	ENSP00000411606.1:n.304-5A>C
ENST00000540753.5:c.542A>C	ENSP00000437709.1:p.His181Pro
ENST00000614910.4:c.473A>C	ENSP00000484800.1:p.His158Pro
ENST00000619306.4:c.710A>C	ENSP00000483540.1:p.His237Pro
NM_000962.3:c.617A>C	NP_000953.2:p.His206Pro
NM_001271164.1:c.473A>C	NP_001258093.1:p.His158Pro
NM_001271165.1:c.290A>C	NP_001258094.1:p.His97Pro
NM_001271166.1:c.290A>C	NP_001258095.1:p.His97Pro
NM_001271367.1:c.290A>C	NP_001258296.1:p.His97Pro
NM_001271368.1:c.542A>C	NP_001258297.1:p.His181Pro
NM_080591.2:c.617A>C	NP_542158.1:p.His206Pro
XM_005252105.2:c.542A>C	XP_005252162.1:p.His181Pro
XM_011518875.1:c.542A>C	XP_011517177.1:p.His181Pro
XM_011518876.1:c.290A>C	XP_011517178.1:p.His97Pro
XM_005252105.3:c.542A>C	XP_005252162.1:p.His181Pro
XM_011518875.2:c.542A>C	XP_011517177.1:p.His181Pro
XM_011518876.2:c.290A>C	XP_011517178.1:p.His97Pro
XM_024447614.1:c.290A>C	XP_024303382.1:p.His97Pro
XM_024447615.1:c.290A>C	XP_024303383.1:p.His97Pro
NM_000962.4:c.617A>C MANE Select	NP_000953.2:p.His206Pro
NM_001271164.2:c.473A>C	NP_001258093.1:p.His158Pro
NM_001271165.2:c.290A>C	NP_001258094.1:p.His97Pro
NM_001271166.2:c.290A>C	NP_001258095.1:p.His97Pro
NM_001271367.2:c.290A>C	NP_001258296.1:p.His97Pro
NM_001271368.2:c.542A>C	NP_001258297.1:p.His181Pro
NM_080591.3:c.617A>C	NP_542158.1:p.His206Pro