Canonical Allele Identifier: CA2691550193
Gene: PTGS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122370999_122371000insGGGGG , CM000671.2:g.122370999_122371000insGGGGG GRCh38
NC_000009.11:g.125133278_125133279insGGGGG , CM000671.1:g.125133278_125133279insGGGGG GRCh37
NC_000009.10:g.124173099_124173100insGGGGG NCBI36
NG_032900.1:g.5050_5051insGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000540753.6:c.-291+157_-291+158insGGGGG ENSP00000437709.1:n.-291+157_-291+158insGGGGG
ENST00000643810.1:c.-321+157_-321+158insGGGGG ENSP00000494717.1:n.-321+157_-321+158insGGGGG
ENST00000540753.5:c.-291+157_-291+158insGGGGG ENSP00000437709.1:n.-291+157_-291+158insGGGGG
NM_001271166.1:c.-321+157_-321+158insGGGGG NP_001258095.1:n.-321+157_-321+158insGGGGG
NM_001271368.1:c.-291+157_-291+158insGGGGG NP_001258297.1:n.-291+157_-291+158insGGGGG
XM_011518875.1:c.-291+157_-291+158insGGGGG XP_011517177.1:n.-291+157_-291+158insGGGGG
XM_011518876.1:c.-4153+157_-4153+158insGGGGG XP_011517178.1:n.-4153+157_-4153+158insGGGGG
XM_011518875.2:c.-291+157_-291+158insGGGGG XP_011517177.1:n.-291+157_-291+158insGGGGG
XM_011518876.2:c.-4153+157_-4153+158insGGGGG XP_011517178.1:n.-4153+157_-4153+158insGGGGG
XM_024447614.1:c.-321+157_-321+158insGGGGG XP_024303382.1:n.-321+157_-321+158insGGGGG
XM_024447615.1:c.-321+157_-321+158insGGGGG XP_024303383.1:n.-321+157_-321+158insGGGGG
NM_001271166.2:c.-321+157_-321+158insGGGGG NP_001258095.1:n.-321+157_-321+158insGGGGG
NM_001271368.2:c.-291+157_-291+158insGGGGG NP_001258297.1:n.-291+157_-291+158insGGGGG