Canonical Allele Identifier: CA1877490269

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370867_122370868delinsGA , CM000671.2:g.122370867_122370868delinsGA	GRCh38
NC_000009.11:g.125133146_125133147delinsGA , CM000671.1:g.125133146_125133147delinsGA	GRCh37
NC_000009.10:g.124172967_124172968delinsGA	NCBI36
NG_032900.1:g.4918_4919delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+25_-291+26delinsGA	ENSP00000437709.1:n.-291+25_-291+26delinsGA
ENST00000643810.1:c.-321+25_-321+26delinsGA	ENSP00000494717.1:n.-321+25_-321+26delinsGA
ENST00000540753.5:c.-291+25_-291+26delinsGA	ENSP00000437709.1:n.-291+25_-291+26delinsGA
NM_001271166.1:c.-321+25_-321+26delinsGA	NP_001258095.1:n.-321+25_-321+26delinsGA
NM_001271368.1:c.-291+25_-291+26delinsGA	NP_001258297.1:n.-291+25_-291+26delinsGA
XM_011518875.1:c.-291+25_-291+26delinsGA	XP_011517177.1:n.-291+25_-291+26delinsGA
XM_011518876.1:c.-4153+25_-4153+26delinsGA	XP_011517178.1:n.-4153+25_-4153+26delinsGA
XM_011518875.2:c.-291+25_-291+26delinsGA	XP_011517177.1:n.-291+25_-291+26delinsGA
XM_011518876.2:c.-4153+25_-4153+26delinsGA	XP_011517178.1:n.-4153+25_-4153+26delinsGA
XM_024447614.1:c.-321+25_-321+26delinsGA	XP_024303382.1:n.-321+25_-321+26delinsGA
XM_024447615.1:c.-321+25_-321+26delinsGA	XP_024303383.1:n.-321+25_-321+26delinsGA
NM_001271166.2:c.-321+25_-321+26delinsGA	NP_001258095.1:n.-321+25_-321+26delinsGA
NM_001271368.2:c.-291+25_-291+26delinsGA	NP_001258297.1:n.-291+25_-291+26delinsGA