Canonical Allele Identifier: CA590503346

Gene: PTGS1

Linked Data

• dbSNP Id: rs1564136962
• gnomAD v2: 9-125143688-C-CAGGA
• gnomAD v4: 9-122381409-C-CAGGA
• MyVariant Identifiers: chr9:g.125143688_125143689insAGGA (hg19) ; chr9:g.122381409_122381410insAGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381409_122381410insAGGA , CM000671.2:g.122381409_122381410insAGGA	GRCh38
NC_000009.11:g.125143688_125143689insAGGA , CM000671.1:g.125143688_125143689insAGGA	GRCh37
NC_000009.10:g.124183509_124183510insAGGA	NCBI36
NG_032900.1:g.15460_15461insAGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.535_536insAGGA MANE Select	ENSP00000354612.2:p.Arg179GlnfsTer12
ENST00000373698.7:c.208_209insAGGA	ENSP00000362802.5:p.Arg70GlnfsTer12
ENST00000426608.6:c.313-87_313-86insAGGA	ENSP00000411606.2:n.313-87_313-86insAGGA
ENST00000540753.6:c.460_461insAGGA	ENSP00000437709.1:p.Arg154GlnfsTer12
ENST00000619306.5:c.391_392insAGGA	ENSP00000483540.2:p.Arg131GlnfsTer12
ENST00000643576.1:n.629_630insAGGA
ENST00000643810.1:c.208_209insAGGA	ENSP00000494717.1:p.Arg70GlnfsTer12
ENST00000645132.1:n.519+2836_519+2837insAGGA
ENST00000647067.1:c.*380_*381insAGGA	ENSP00000495728.1:n.*380_*381insAGGA
ENST00000223423.8:c.535_536insAGGA	ENSP00000223423.4:p.Arg179GlnfsTer12
ENST00000362012.6:c.535_536insAGGA	ENSP00000354612.2:p.Arg179GlnfsTer12
ENST00000373698.6:c.208_209insAGGA	ENSP00000362802.5:p.Arg70GlnfsTer12
ENST00000426608.5:c.304-87_304-86insAGGA	ENSP00000411606.1:n.304-87_304-86insAGGA
ENST00000540753.5:c.460_461insAGGA	ENSP00000437709.1:p.Arg154GlnfsTer12
ENST00000614910.4:c.391_392insAGGA	ENSP00000484800.1:p.Arg131GlnfsTer12
ENST00000619306.4:c.628_629insAGGA	ENSP00000483540.1:p.Arg210GlnfsTer12
NM_000962.3:c.535_536insAGGA	NP_000953.2:p.Arg179GlnfsTer12
NM_001271164.1:c.391_392insAGGA	NP_001258093.1:p.Arg131GlnfsTer12
NM_001271165.1:c.208_209insAGGA	NP_001258094.1:p.Arg70GlnfsTer12
NM_001271166.1:c.208_209insAGGA	NP_001258095.1:p.Arg70GlnfsTer12
NM_001271367.1:c.208_209insAGGA	NP_001258296.1:p.Arg70GlnfsTer12
NM_001271368.1:c.460_461insAGGA	NP_001258297.1:p.Arg154GlnfsTer12
NM_080591.2:c.535_536insAGGA	NP_542158.1:p.Arg179GlnfsTer12
XM_005252105.2:c.460_461insAGGA	XP_005252162.1:p.Arg154GlnfsTer12
XM_011518875.1:c.460_461insAGGA	XP_011517177.1:p.Arg154GlnfsTer12
XM_011518876.1:c.208_209insAGGA	XP_011517178.1:p.Arg70GlnfsTer12
XM_005252105.3:c.460_461insAGGA	XP_005252162.1:p.Arg154GlnfsTer12
XM_011518875.2:c.460_461insAGGA	XP_011517177.1:p.Arg154GlnfsTer12
XM_011518876.2:c.208_209insAGGA	XP_011517178.1:p.Arg70GlnfsTer12
XM_024447614.1:c.208_209insAGGA	XP_024303382.1:p.Arg70GlnfsTer12
XM_024447615.1:c.208_209insAGGA	XP_024303383.1:p.Arg70GlnfsTer12
NM_000962.4:c.535_536insAGGA MANE Select	NP_000953.2:p.Arg179GlnfsTer12
NM_001271164.2:c.391_392insAGGA	NP_001258093.1:p.Arg131GlnfsTer12
NM_001271165.2:c.208_209insAGGA	NP_001258094.1:p.Arg70GlnfsTer12
NM_001271166.2:c.208_209insAGGA	NP_001258095.1:p.Arg70GlnfsTer12
NM_001271367.2:c.208_209insAGGA	NP_001258296.1:p.Arg70GlnfsTer12
NM_001271368.2:c.460_461insAGGA	NP_001258297.1:p.Arg154GlnfsTer12
NM_080591.3:c.535_536insAGGA	NP_542158.1:p.Arg179GlnfsTer12