Canonical Allele Identifier: CA374780464

Gene: PTGS1

Linked Data

• dbSNP Id: rs1837505888
• gnomAD v4: 9-122381403-G-A
• MyVariant Identifiers: chr9:g.125143682G>A (hg19) ; chr9:g.122381403G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381403G>A , CM000671.2:g.122381403G>A	GRCh38
NC_000009.11:g.125143682G>A , CM000671.1:g.125143682G>A	GRCh37
NC_000009.10:g.124183503G>A	NCBI36
NG_032900.1:g.15454G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.529G>A MANE Select	ENSP00000354612.2:p.Ala177Thr
ENST00000373698.7:c.202G>A	ENSP00000362802.5:p.Ala68Thr
ENST00000426608.6:c.313-93G>A	ENSP00000411606.2:n.313-93G>A
ENST00000540753.6:c.454G>A	ENSP00000437709.1:p.Ala152Thr
ENST00000619306.5:c.385G>A	ENSP00000483540.2:p.Ala129Thr
ENST00000643576.1:n.623G>A
ENST00000643810.1:c.202G>A	ENSP00000494717.1:p.Ala68Thr
ENST00000645132.1:n.519+2830G>A
ENST00000647067.1:c.*374G>A	ENSP00000495728.1:n.*374G>A
ENST00000223423.8:c.529G>A	ENSP00000223423.4:p.Ala177Thr
ENST00000362012.6:c.529G>A	ENSP00000354612.2:p.Ala177Thr
ENST00000373698.6:c.202G>A	ENSP00000362802.5:p.Ala68Thr
ENST00000426608.5:c.304-93G>A	ENSP00000411606.1:n.304-93G>A
ENST00000540753.5:c.454G>A	ENSP00000437709.1:p.Ala152Thr
ENST00000614910.4:c.385G>A	ENSP00000484800.1:p.Ala129Thr
ENST00000619306.4:c.622G>A	ENSP00000483540.1:p.Ala208Thr
NM_000962.3:c.529G>A	NP_000953.2:p.Ala177Thr
NM_001271164.1:c.385G>A	NP_001258093.1:p.Ala129Thr
NM_001271165.1:c.202G>A	NP_001258094.1:p.Ala68Thr
NM_001271166.1:c.202G>A	NP_001258095.1:p.Ala68Thr
NM_001271367.1:c.202G>A	NP_001258296.1:p.Ala68Thr
NM_001271368.1:c.454G>A	NP_001258297.1:p.Ala152Thr
NM_080591.2:c.529G>A	NP_542158.1:p.Ala177Thr
XM_005252105.2:c.454G>A	XP_005252162.1:p.Ala152Thr
XM_011518875.1:c.454G>A	XP_011517177.1:p.Ala152Thr
XM_011518876.1:c.202G>A	XP_011517178.1:p.Ala68Thr
XM_005252105.3:c.454G>A	XP_005252162.1:p.Ala152Thr
XM_011518875.2:c.454G>A	XP_011517177.1:p.Ala152Thr
XM_011518876.2:c.202G>A	XP_011517178.1:p.Ala68Thr
XM_024447614.1:c.202G>A	XP_024303382.1:p.Ala68Thr
XM_024447615.1:c.202G>A	XP_024303383.1:p.Ala68Thr
NM_000962.4:c.529G>A MANE Select	NP_000953.2:p.Ala177Thr
NM_001271164.2:c.385G>A	NP_001258093.1:p.Ala129Thr
NM_001271165.2:c.202G>A	NP_001258094.1:p.Ala68Thr
NM_001271166.2:c.202G>A	NP_001258095.1:p.Ala68Thr
NM_001271367.2:c.202G>A	NP_001258296.1:p.Ala68Thr
NM_001271368.2:c.454G>A	NP_001258297.1:p.Ala152Thr
NM_080591.3:c.529G>A	NP_542158.1:p.Ala177Thr