Canonical Allele Identifier: CA1128879566

Gene: PTGS1

Linked Data

• dbSNP Id: rs1836752048
• gnomAD v3: 9-122370810-TG-T
• gnomAD v4: 9-122370810-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370811del , CM000671.2:g.122370811del	GRCh38
NC_000009.11:g.125133090del , CM000671.1:g.125133090del	GRCh37
NC_000009.10:g.124172911del	NCBI36
NG_032900.1:g.4862del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-322del	ENSP00000437709.1:n.-322del
ENST00000643810.1:c.-352del	ENSP00000494717.1:n.-352del
ENST00000540753.5:c.-322del	ENSP00000437709.1:n.-322del
NM_001271166.1:c.-352del	NP_001258095.1:n.-352del
NM_001271368.1:c.-322del	NP_001258297.1:n.-322del
XM_011518875.1:c.-322del	XP_011517177.1:n.-322del
XM_011518876.1:c.-4184del	XP_011517178.1:n.-4184del
XM_011518875.2:c.-322del	XP_011517177.1:n.-322del
XM_011518876.2:c.-4184del	XP_011517178.1:n.-4184del
XM_024447614.1:c.-352del	XP_024303382.1:n.-352del
XM_024447615.1:c.-352del	XP_024303383.1:n.-352del
NM_001271166.2:c.-352del	NP_001258095.1:n.-352del
NM_001271368.2:c.-322del	NP_001258297.1:n.-322del