Canonical Allele Identifier: CA645560782

Gene: PTGS1

Linked Data

• COSMIC: COSM381683

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381490_122381491delinsTT , CM000671.2:g.122381490_122381491delinsTT	GRCh38
NC_000009.11:g.125143769_125143770delinsTT , CM000671.1:g.125143769_125143770delinsTT	GRCh37
NC_000009.10:g.124183590_124183591delinsTT	NCBI36
NG_032900.1:g.15541_15542delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.616_617delinsTT MANE Select	ENSP00000354612.2:p.His206Phe
ENST00000373698.7:c.289_290delinsTT	ENSP00000362802.5:p.His97Phe
ENST00000426608.6:c.313-6_313-5delinsTT	ENSP00000411606.2:n.313-6_313-5delinsTT
ENST00000540753.6:c.541_542delinsTT	ENSP00000437709.1:p.His181Phe
ENST00000619306.5:c.472_473delinsTT	ENSP00000483540.2:p.His158Phe
ENST00000643576.1:n.710_711delinsTT
ENST00000643810.1:c.289_290delinsTT	ENSP00000494717.1:p.His97Phe
ENST00000645132.1:n.519+2917_519+2918delinsTT
ENST00000647067.1:c.*461_*462delinsTT	ENSP00000495728.1:n.*461_*462delinsTT
ENST00000223423.8:c.616_617delinsTT	ENSP00000223423.4:p.His206Phe
ENST00000362012.6:c.616_617delinsTT	ENSP00000354612.2:p.His206Phe
ENST00000373698.6:c.289_290delinsTT	ENSP00000362802.5:p.His97Phe
ENST00000426608.5:c.304-6_304-5delinsTT	ENSP00000411606.1:n.304-6_304-5delinsTT
ENST00000540753.5:c.541_542delinsTT	ENSP00000437709.1:p.His181Phe
ENST00000614910.4:c.472_473delinsTT	ENSP00000484800.1:p.His158Phe
ENST00000619306.4:c.709_710delinsTT	ENSP00000483540.1:p.His237Phe
NM_000962.3:c.616_617delinsTT	NP_000953.2:p.His206Phe
NM_001271164.1:c.472_473delinsTT	NP_001258093.1:p.His158Phe
NM_001271165.1:c.289_290delinsTT	NP_001258094.1:p.His97Phe
NM_001271166.1:c.289_290delinsTT	NP_001258095.1:p.His97Phe
NM_001271367.1:c.289_290delinsTT	NP_001258296.1:p.His97Phe
NM_001271368.1:c.541_542delinsTT	NP_001258297.1:p.His181Phe
NM_080591.2:c.616_617delinsTT	NP_542158.1:p.His206Phe
XM_005252105.2:c.541_542delinsTT	XP_005252162.1:p.His181Phe
XM_011518875.1:c.541_542delinsTT	XP_011517177.1:p.His181Phe
XM_011518876.1:c.289_290delinsTT	XP_011517178.1:p.His97Phe
XM_005252105.3:c.541_542delinsTT	XP_005252162.1:p.His181Phe
XM_011518875.2:c.541_542delinsTT	XP_011517177.1:p.His181Phe
XM_011518876.2:c.289_290delinsTT	XP_011517178.1:p.His97Phe
XM_024447614.1:c.289_290delinsTT	XP_024303382.1:p.His97Phe
XM_024447615.1:c.289_290delinsTT	XP_024303383.1:p.His97Phe
NM_000962.4:c.616_617delinsTT MANE Select	NP_000953.2:p.His206Phe
NM_001271164.2:c.472_473delinsTT	NP_001258093.1:p.His158Phe
NM_001271165.2:c.289_290delinsTT	NP_001258094.1:p.His97Phe
NM_001271166.2:c.289_290delinsTT	NP_001258095.1:p.His97Phe
NM_001271367.2:c.289_290delinsTT	NP_001258296.1:p.His97Phe
NM_001271368.2:c.541_542delinsTT	NP_001258297.1:p.His181Phe
NM_080591.3:c.616_617delinsTT	NP_542158.1:p.His206Phe