Canonical Allele Identifier: CA2691549980

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122370762-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370765del , CM000671.2:g.122370765del	GRCh38
NC_000009.11:g.125133044del , CM000671.1:g.125133044del	GRCh37
NC_000009.10:g.124172865del	NCBI36
NG_032900.1:g.4816del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-368del	ENSP00000437709.1:n.-368del
ENST00000643810.1:c.-398del	ENSP00000494717.1:n.-398del
ENST00000540753.5:c.-368del	ENSP00000437709.1:n.-368del
NM_001271166.1:c.-398del	NP_001258095.1:n.-398del
NM_001271368.1:c.-368del	NP_001258297.1:n.-368del
XM_011518875.1:c.-368del	XP_011517177.1:n.-368del
XM_011518876.1:c.-4230del	XP_011517178.1:n.-4230del
XM_011518875.2:c.-368del	XP_011517177.1:n.-368del
XM_011518876.2:c.-4230del	XP_011517178.1:n.-4230del
XM_024447614.1:c.-398del	XP_024303382.1:n.-398del
XM_024447615.1:c.-398del	XP_024303383.1:n.-398del
NM_001271166.2:c.-398del	NP_001258095.1:n.-398del
NM_001271368.2:c.-368del	NP_001258297.1:n.-368del