Canonical Allele Identifier: CA1128881693

Gene: PTGS1

Linked Data

• gnomAD v3: 9-122381459-C-CATTTAGAAAGCTG
• gnomAD v4: 9-122381459-C-CATTTAGAAAGCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381461_122381462insTTAGAAAGCTGAT , CM000671.2:g.122381461_122381462insTTAGAAAGCTGAT	GRCh38
NC_000009.11:g.125143740_125143741insTTAGAAAGCTGAT , CM000671.1:g.125143740_125143741insTTAGAAAGCTGAT	GRCh37
NC_000009.10:g.124183561_124183562insTTAGAAAGCTGAT	NCBI36
NG_032900.1:g.15512_15513insTTAGAAAGCTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.587_588insTTAGAAAGCTGAT MANE Select	ENSP00000354612.2:p.Met196IlefsTer2
ENST00000373698.7:c.260_261insTTAGAAAGCTGAT	ENSP00000362802.5:p.Met87IlefsTer2
ENST00000426608.6:c.313-35_313-34insTTAGAAAGCTGAT	ENSP00000411606.2:n.313-35_313-34insTTAGAAAGCTGAT
ENST00000540753.6:c.512_513insTTAGAAAGCTGAT	ENSP00000437709.1:p.Met171IlefsTer2
ENST00000619306.5:c.443_444insTTAGAAAGCTGAT	ENSP00000483540.2:p.Met148IlefsTer2
ENST00000643576.1:n.681_682insTTAGAAAGCTGAT
ENST00000643810.1:c.260_261insTTAGAAAGCTGAT	ENSP00000494717.1:p.Met87IlefsTer2
ENST00000645132.1:n.519+2888_519+2889insTTAGAAAGCTGAT
ENST00000647067.1:c.*432_*433insTTAGAAAGCTGAT	ENSP00000495728.1:n.*432_*433insTTAGAAAGCTGAT
ENST00000223423.8:c.587_588insTTAGAAAGCTGAT	ENSP00000223423.4:p.Met196IlefsTer2
ENST00000362012.6:c.587_588insTTAGAAAGCTGAT	ENSP00000354612.2:p.Met196IlefsTer2
ENST00000373698.6:c.260_261insTTAGAAAGCTGAT	ENSP00000362802.5:p.Met87IlefsTer2
ENST00000426608.5:c.304-35_304-34insTTAGAAAGCTGAT	ENSP00000411606.1:n.304-35_304-34insTTAGAAAGCTGAT
ENST00000540753.5:c.512_513insTTAGAAAGCTGAT	ENSP00000437709.1:p.Met171IlefsTer2
ENST00000614910.4:c.443_444insTTAGAAAGCTGAT	ENSP00000484800.1:p.Met148IlefsTer2
ENST00000619306.4:c.680_681insTTAGAAAGCTGAT	ENSP00000483540.1:p.Met227IlefsTer2
NM_000962.3:c.587_588insTTAGAAAGCTGAT	NP_000953.2:p.Met196IlefsTer2
NM_001271164.1:c.443_444insTTAGAAAGCTGAT	NP_001258093.1:p.Met148IlefsTer2
NM_001271165.1:c.260_261insTTAGAAAGCTGAT	NP_001258094.1:p.Met87IlefsTer2
NM_001271166.1:c.260_261insTTAGAAAGCTGAT	NP_001258095.1:p.Met87IlefsTer2
NM_001271367.1:c.260_261insTTAGAAAGCTGAT	NP_001258296.1:p.Met87IlefsTer2
NM_001271368.1:c.512_513insTTAGAAAGCTGAT	NP_001258297.1:p.Met171IlefsTer2
NM_080591.2:c.587_588insTTAGAAAGCTGAT	NP_542158.1:p.Met196IlefsTer2
XM_005252105.2:c.512_513insTTAGAAAGCTGAT	XP_005252162.1:p.Met171IlefsTer2
XM_011518875.1:c.512_513insTTAGAAAGCTGAT	XP_011517177.1:p.Met171IlefsTer2
XM_011518876.1:c.260_261insTTAGAAAGCTGAT	XP_011517178.1:p.Met87IlefsTer2
XM_005252105.3:c.512_513insTTAGAAAGCTGAT	XP_005252162.1:p.Met171IlefsTer2
XM_011518875.2:c.512_513insTTAGAAAGCTGAT	XP_011517177.1:p.Met171IlefsTer2
XM_011518876.2:c.260_261insTTAGAAAGCTGAT	XP_011517178.1:p.Met87IlefsTer2
XM_024447614.1:c.260_261insTTAGAAAGCTGAT	XP_024303382.1:p.Met87IlefsTer2
XM_024447615.1:c.260_261insTTAGAAAGCTGAT	XP_024303383.1:p.Met87IlefsTer2
NM_000962.4:c.587_588insTTAGAAAGCTGAT MANE Select	NP_000953.2:p.Met196IlefsTer2
NM_001271164.2:c.443_444insTTAGAAAGCTGAT	NP_001258093.1:p.Met148IlefsTer2
NM_001271165.2:c.260_261insTTAGAAAGCTGAT	NP_001258094.1:p.Met87IlefsTer2
NM_001271166.2:c.260_261insTTAGAAAGCTGAT	NP_001258095.1:p.Met87IlefsTer2
NM_001271367.2:c.260_261insTTAGAAAGCTGAT	NP_001258296.1:p.Met87IlefsTer2
NM_001271368.2:c.512_513insTTAGAAAGCTGAT	NP_001258297.1:p.Met171IlefsTer2
NM_080591.3:c.587_588insTTAGAAAGCTGAT	NP_542158.1:p.Met196IlefsTer2