Canonical Allele Identifier: CA2691551906

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122381392-CCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381393_122381395del , CM000671.2:g.122381393_122381395del	GRCh38
NC_000009.11:g.125143672_125143674del , CM000671.1:g.125143672_125143674del	GRCh37
NC_000009.10:g.124183493_124183495del	NCBI36
NG_032900.1:g.15444_15446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362012.7:c.519_521del MANE Select	ENSP00000354612.2:p.Gln174del
ENST00000373698.7:c.192_194del	ENSP00000362802.5:p.Gln65del
ENST00000426608.6:c.313-103_313-101del	ENSP00000411606.2:n.313-103_313-101del
ENST00000540753.6:c.444_446del	ENSP00000437709.1:p.Gln149del
ENST00000619306.5:c.375_377del	ENSP00000483540.2:p.Gln126del
ENST00000643576.1:n.613_615del
ENST00000643810.1:c.192_194del	ENSP00000494717.1:p.Gln65del
ENST00000645132.1:n.519+2820_519+2822del
ENST00000647067.1:c.*364_*366del	ENSP00000495728.1:n.*364_*366del
ENST00000223423.8:c.519_521del	ENSP00000223423.4:p.Gln174del
ENST00000362012.6:c.519_521del	ENSP00000354612.2:p.Gln174del
ENST00000373698.6:c.192_194del	ENSP00000362802.5:p.Gln65del
ENST00000426608.5:c.304-103_304-101del	ENSP00000411606.1:n.304-103_304-101del
ENST00000540753.5:c.444_446del	ENSP00000437709.1:p.Gln149del
ENST00000614910.4:c.375_377del	ENSP00000484800.1:p.Gln126del
ENST00000619306.4:c.612_614del	ENSP00000483540.1:p.Gln205del
NM_000962.3:c.519_521del	NP_000953.2:p.Gln174del
NM_001271164.1:c.375_377del	NP_001258093.1:p.Gln126del
NM_001271165.1:c.192_194del	NP_001258094.1:p.Gln65del
NM_001271166.1:c.192_194del	NP_001258095.1:p.Gln65del
NM_001271367.1:c.192_194del	NP_001258296.1:p.Gln65del
NM_001271368.1:c.444_446del	NP_001258297.1:p.Gln149del
NM_080591.2:c.519_521del	NP_542158.1:p.Gln174del
XM_005252105.2:c.444_446del	XP_005252162.1:p.Gln149del
XM_011518875.1:c.444_446del	XP_011517177.1:p.Gln149del
XM_011518876.1:c.192_194del	XP_011517178.1:p.Gln65del
XM_005252105.3:c.444_446del	XP_005252162.1:p.Gln149del
XM_011518875.2:c.444_446del	XP_011517177.1:p.Gln149del
XM_011518876.2:c.192_194del	XP_011517178.1:p.Gln65del
XM_024447614.1:c.192_194del	XP_024303382.1:p.Gln65del
XM_024447615.1:c.192_194del	XP_024303383.1:p.Gln65del
NM_000962.4:c.519_521del MANE Select	NP_000953.2:p.Gln174del
NM_001271164.2:c.375_377del	NP_001258093.1:p.Gln126del
NM_001271165.2:c.192_194del	NP_001258094.1:p.Gln65del
NM_001271166.2:c.192_194del	NP_001258095.1:p.Gln65del
NM_001271367.2:c.192_194del	NP_001258296.1:p.Gln65del
NM_001271368.2:c.444_446del	NP_001258297.1:p.Gln149del
NM_080591.3:c.519_521del	NP_542158.1:p.Gln174del