Canonical Allele Identifier: CA2785849926

Gene: PTGS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370989_122370990insGGGGGTTGGGGCGGGGGG , CM000671.2:g.122370989_122370990insGGGGGTTGGGGCGGGGGG	GRCh38
NC_000009.11:g.125133268_125133269insGGGGGTTGGGGCGGGGGG , CM000671.1:g.125133268_125133269insGGGGGTTGGGGCGGGGGG	GRCh37
NC_000009.10:g.124173089_124173090insGGGGGTTGGGGCGGGGGG	NCBI36
NG_032900.1:g.5040_5041insGGGGGTTGGGGCGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-291+147_-291+148insGGGGGTTGGGGCGGGGGG	ENSP00000437709.1:n.-291+147_-291+148insGGGGGTTGGGGCGGGGGG
ENST00000643810.1:c.-321+147_-321+148insGGGGGTTGGGGCGGGGGG	ENSP00000494717.1:n.-321+147_-321+148insGGGGGTTGGGGCGGGGGG
ENST00000540753.5:c.-291+147_-291+148insGGGGGTTGGGGCGGGGGG	ENSP00000437709.1:n.-291+147_-291+148insGGGGGTTGGGGCGGGGGG
NM_001271166.1:c.-321+147_-321+148insGGGGGTTGGGGCGGGGGG	NP_001258095.1:n.-321+147_-321+148insGGGGGTTGGGGCGGGGGG
NM_001271368.1:c.-291+147_-291+148insGGGGGTTGGGGCGGGGGG	NP_001258297.1:n.-291+147_-291+148insGGGGGTTGGGGCGGGGGG
XM_011518875.1:c.-291+147_-291+148insGGGGGTTGGGGCGGGGGG	XP_011517177.1:n.-291+147_-291+148insGGGGGTTGGGGCGGGGGG
XM_011518876.1:c.-4153+147_-4153+148insGGGGGTTGGGGCGGGGGG	XP_011517178.1:n.-4153+147_-4153+148insGGGGGTTGGGGCGGGGGG
XM_011518875.2:c.-291+147_-291+148insGGGGGTTGGGGCGGGGGG	XP_011517177.1:n.-291+147_-291+148insGGGGGTTGGGGCGGGGGG
XM_011518876.2:c.-4153+147_-4153+148insGGGGGTTGGGGCGGGGGG	XP_011517178.1:n.-4153+147_-4153+148insGGGGGTTGGGGCGGGGGG
XM_024447614.1:c.-321+147_-321+148insGGGGGTTGGGGCGGGGGG	XP_024303382.1:n.-321+147_-321+148insGGGGGTTGGGGCGGGGGG
XM_024447615.1:c.-321+147_-321+148insGGGGGTTGGGGCGGGGGG	XP_024303383.1:n.-321+147_-321+148insGGGGGTTGGGGCGGGGGG
NM_001271166.2:c.-321+147_-321+148insGGGGGTTGGGGCGGGGGG	NP_001258095.1:n.-321+147_-321+148insGGGGGTTGGGGCGGGGGG
NM_001271368.2:c.-291+147_-291+148insGGGGGTTGGGGCGGGGGG	NP_001258297.1:n.-291+147_-291+148insGGGGGTTGGGGCGGGGGG