Canonical Allele Identifier: CA1128881691

Gene: PTGS1

Linked Data

• gnomAD v3: 9-122381457-C-CCACTTACGGGCCAGCTGCATAAAAA
• gnomAD v4: 9-122381457-C-CCACTTACGGGCCAGCTGCATAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381457_122381458insCACTTACGGGCCAGCTGCATAAAAA , CM000671.2:g.122381457_122381458insCACTTACGGGCCAGCTGCATAAAAA	GRCh38
NC_000009.11:g.125143736_125143737insCACTTACGGGCCAGCTGCATAAAAA , CM000671.1:g.125143736_125143737insCACTTACGGGCCAGCTGCATAAAAA	GRCh37
NC_000009.10:g.124183557_124183558insCACTTACGGGCCAGCTGCATAAAAA	NCBI36
NG_032900.1:g.15508_15509insCACTTACGGGCCAGCTGCATAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.583_584insCACTTACGGGCCAGCTGCATAAAAA MANE Select	ENSP00000354612.2:p.Leu195ProfsTer?
ENST00000373698.7:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000362802.5:p.Leu86ProfsTer?
ENST00000426608.6:c.313-39_313-38insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000411606.2:n.313-39_313-38insCACTTACGGGCCAGCTGCATAAAAA...
ENST00000540753.6:c.508_509insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000437709.1:p.Leu170ProfsTer?
ENST00000619306.5:c.439_440insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000483540.2:p.Leu147ProfsTer?
ENST00000643576.1:n.677_678insCACTTACGGGCCAGCTGCATAAAAA
ENST00000643810.1:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000494717.1:p.Leu86ProfsTer?
ENST00000645132.1:n.519+2884_519+2885insCACTTACGGGCCAGCTGCATAAAAA
ENST00000647067.1:c.*428_*429insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000495728.1:n.*428_*429insCACTTACGGGCCAGCTGCATAAAAA
ENST00000223423.8:c.583_584insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000223423.4:p.Leu195ProfsTer?
ENST00000362012.6:c.583_584insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000354612.2:p.Leu195ProfsTer?
ENST00000373698.6:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000362802.5:p.Leu86ProfsTer?
ENST00000426608.5:c.304-39_304-38insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000411606.1:n.304-39_304-38insCACTTACGGGCCAGCTGCATAAAAA...
ENST00000540753.5:c.508_509insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000437709.1:p.Leu170ProfsTer?
ENST00000614910.4:c.439_440insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000484800.1:p.Leu147ProfsTer?
ENST00000619306.4:c.676_677insCACTTACGGGCCAGCTGCATAAAAA	ENSP00000483540.1:p.Leu226ProfsTer?
NM_000962.3:c.583_584insCACTTACGGGCCAGCTGCATAAAAA	NP_000953.2:p.Leu195ProfsTer?
NM_001271164.1:c.439_440insCACTTACGGGCCAGCTGCATAAAAA	NP_001258093.1:p.Leu147ProfsTer?
NM_001271165.1:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	NP_001258094.1:p.Leu86ProfsTer?
NM_001271166.1:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	NP_001258095.1:p.Leu86ProfsTer?
NM_001271367.1:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	NP_001258296.1:p.Leu86ProfsTer?
NM_001271368.1:c.508_509insCACTTACGGGCCAGCTGCATAAAAA	NP_001258297.1:p.Leu170ProfsTer?
NM_080591.2:c.583_584insCACTTACGGGCCAGCTGCATAAAAA	NP_542158.1:p.Leu195ProfsTer?
XM_005252105.2:c.508_509insCACTTACGGGCCAGCTGCATAAAAA	XP_005252162.1:p.Leu170ProfsTer?
XM_011518875.1:c.508_509insCACTTACGGGCCAGCTGCATAAAAA	XP_011517177.1:p.Leu170ProfsTer?
XM_011518876.1:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	XP_011517178.1:p.Leu86ProfsTer?
XM_005252105.3:c.508_509insCACTTACGGGCCAGCTGCATAAAAA	XP_005252162.1:p.Leu170ProfsTer?
XM_011518875.2:c.508_509insCACTTACGGGCCAGCTGCATAAAAA	XP_011517177.1:p.Leu170ProfsTer?
XM_011518876.2:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	XP_011517178.1:p.Leu86ProfsTer?
XM_024447614.1:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	XP_024303382.1:p.Leu86ProfsTer?
XM_024447615.1:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	XP_024303383.1:p.Leu86ProfsTer?
NM_000962.4:c.583_584insCACTTACGGGCCAGCTGCATAAAAA MANE Select	NP_000953.2:p.Leu195ProfsTer?
NM_001271164.2:c.439_440insCACTTACGGGCCAGCTGCATAAAAA	NP_001258093.1:p.Leu147ProfsTer?
NM_001271165.2:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	NP_001258094.1:p.Leu86ProfsTer?
NM_001271166.2:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	NP_001258095.1:p.Leu86ProfsTer?
NM_001271367.2:c.256_257insCACTTACGGGCCAGCTGCATAAAAA	NP_001258296.1:p.Leu86ProfsTer?
NM_001271368.2:c.508_509insCACTTACGGGCCAGCTGCATAAAAA	NP_001258297.1:p.Leu170ProfsTer?
NM_080591.3:c.583_584insCACTTACGGGCCAGCTGCATAAAAA	NP_542158.1:p.Leu195ProfsTer?