Canonical Allele Identifier: CA5224828

Gene: PTGS1

Linked Data

• dbSNP Id: rs748077679
• ExAC: 9:125143637 AC / A
• gnomAD v2: 9-125143637-AC-A
• gnomAD v3: 9-122381358-AC-A
• gnomAD v4: 9-122381358-AC-A
• MyVariant Identifiers: chr9:g.125143638del (hg19) ; chr9:g.122381359del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381364del , CM000671.2:g.122381364del	GRCh38
NC_000009.11:g.125143643del , CM000671.1:g.125143643del	GRCh37
NC_000009.10:g.124183464del	NCBI36
NG_032900.1:g.15415del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.497-7del MANE Select	ENSP00000354612.2:n.497-7del
ENST00000373698.7:c.170-7del	ENSP00000362802.5:n.170-7del
ENST00000426608.6:c.313-132del	ENSP00000411606.2:n.313-132del
ENST00000540753.6:c.422-7del	ENSP00000437709.1:n.422-7del
ENST00000619306.5:c.353-7del	ENSP00000483540.2:n.353-7del
ENST00000643576.1:n.591-7del
ENST00000643810.1:c.170-7del	ENSP00000494717.1:n.170-7del
ENST00000645132.1:n.519+2791del
ENST00000647067.1:c.*342-7del	ENSP00000495728.1:n.*342-7del
ENST00000223423.8:c.497-7del	ENSP00000223423.4:n.497-7del
ENST00000362012.6:c.497-7del	ENSP00000354612.2:n.497-7del
ENST00000373698.6:c.170-7del	ENSP00000362802.5:n.170-7del
ENST00000426608.5:c.304-132del	ENSP00000411606.1:n.304-132del
ENST00000540753.5:c.422-7del	ENSP00000437709.1:n.422-7del
ENST00000614910.4:c.353-7del	ENSP00000484800.1:n.353-7del
ENST00000619306.4:c.590-7del	ENSP00000483540.1:n.590-7del
NM_000962.3:c.497-7del	NP_000953.2:n.497-7del
NM_001271164.1:c.353-7del	NP_001258093.1:n.353-7del
NM_001271165.1:c.170-7del	NP_001258094.1:n.170-7del
NM_001271166.1:c.170-7del	NP_001258095.1:n.170-7del
NM_001271367.1:c.170-7del	NP_001258296.1:n.170-7del
NM_001271368.1:c.422-7del	NP_001258297.1:n.422-7del
NM_080591.2:c.497-7del	NP_542158.1:n.497-7del
XM_005252105.2:c.422-7del	XP_005252162.1:n.422-7del
XM_011518875.1:c.422-7del	XP_011517177.1:n.422-7del
XM_011518876.1:c.170-7del	XP_011517178.1:n.170-7del
XM_005252105.3:c.422-7del	XP_005252162.1:n.422-7del
XM_011518875.2:c.422-7del	XP_011517177.1:n.422-7del
XM_011518876.2:c.170-7del	XP_011517178.1:n.170-7del
XM_024447614.1:c.170-7del	XP_024303382.1:n.170-7del
XM_024447615.1:c.170-7del	XP_024303383.1:n.170-7del
NM_000962.4:c.497-7del MANE Select	NP_000953.2:n.497-7del
NM_001271164.2:c.353-7del	NP_001258093.1:n.353-7del
NM_001271165.2:c.170-7del	NP_001258094.1:n.170-7del
NM_001271166.2:c.170-7del	NP_001258095.1:n.170-7del
NM_001271367.2:c.170-7del	NP_001258296.1:n.170-7del
NM_001271368.2:c.422-7del	NP_001258297.1:n.422-7del
NM_080591.3:c.497-7del	NP_542158.1:n.497-7del