Canonical Allele Identifier: CA2691549982

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122370766-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370769del , CM000671.2:g.122370769del	GRCh38
NC_000009.11:g.125133048del , CM000671.1:g.125133048del	GRCh37
NC_000009.10:g.124172869del	NCBI36
NG_032900.1:g.4820del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-364del	ENSP00000437709.1:n.-364del
ENST00000643810.1:c.-394del	ENSP00000494717.1:n.-394del
ENST00000540753.5:c.-364del	ENSP00000437709.1:n.-364del
NM_001271166.1:c.-394del	NP_001258095.1:n.-394del
NM_001271368.1:c.-364del	NP_001258297.1:n.-364del
XM_011518875.1:c.-364del	XP_011517177.1:n.-364del
XM_011518876.1:c.-4226del	XP_011517178.1:n.-4226del
XM_011518875.2:c.-364del	XP_011517177.1:n.-364del
XM_011518876.2:c.-4226del	XP_011517178.1:n.-4226del
XM_024447614.1:c.-394del	XP_024303382.1:n.-394del
XM_024447615.1:c.-394del	XP_024303383.1:n.-394del
NM_001271166.2:c.-394del	NP_001258095.1:n.-394del
NM_001271368.2:c.-364del	NP_001258297.1:n.-364del