Canonical Allele Identifier: CA2516246815
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122381448_122381449dup , CM000671.2:g.122381448_122381449dup GRCh38
NC_000009.11:g.125143727_125143728dup , CM000671.1:g.125143727_125143728dup GRCh37
NC_000009.10:g.124183548_124183549dup NCBI36
NG_032900.1:g.15499_15500dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000362012.7:c.574_575dup MANE Select ENSP00000354612.2:p.Thr193AlafsTer?
ENST00000373698.7:c.247_248dup ENSP00000362802.5:p.Thr84AlafsTer?
ENST00000426608.6:c.313-48_313-47dup ENSP00000411606.2:n.313-48_313-47dup
ENST00000540753.6:c.499_500dup ENSP00000437709.1:p.Thr168AlafsTer?
ENST00000619306.5:c.430_431dup ENSP00000483540.2:p.Thr145AlafsTer?
ENST00000643576.1:n.668_669dup
ENST00000643810.1:c.247_248dup ENSP00000494717.1:p.Thr84AlafsTer?
ENST00000645132.1:n.519+2875_519+2876dup
ENST00000647067.1:c.*419_*420dup ENSP00000495728.1:n.*419_*420dup
ENST00000223423.8:c.574_575dup ENSP00000223423.4:p.Thr193AlafsTer?
ENST00000362012.6:c.574_575dup ENSP00000354612.2:p.Thr193AlafsTer?
ENST00000373698.6:c.247_248dup ENSP00000362802.5:p.Thr84AlafsTer?
ENST00000426608.5:c.304-48_304-47dup ENSP00000411606.1:n.304-48_304-47dup
ENST00000540753.5:c.499_500dup ENSP00000437709.1:p.Thr168AlafsTer?
ENST00000614910.4:c.430_431dup ENSP00000484800.1:p.Thr145AlafsTer?
ENST00000619306.4:c.667_668dup ENSP00000483540.1:p.Thr224AlafsTer?
NM_000962.3:c.574_575dup NP_000953.2:p.Thr193AlafsTer?
NM_001271164.1:c.430_431dup NP_001258093.1:p.Thr145AlafsTer?
NM_001271165.1:c.247_248dup NP_001258094.1:p.Thr84AlafsTer?
NM_001271166.1:c.247_248dup NP_001258095.1:p.Thr84AlafsTer?
NM_001271367.1:c.247_248dup NP_001258296.1:p.Thr84AlafsTer?
NM_001271368.1:c.499_500dup NP_001258297.1:p.Thr168AlafsTer?
NM_080591.2:c.574_575dup NP_542158.1:p.Thr193AlafsTer?
XM_005252105.2:c.499_500dup XP_005252162.1:p.Thr168AlafsTer?
XM_011518875.1:c.499_500dup XP_011517177.1:p.Thr168AlafsTer?
XM_011518876.1:c.247_248dup XP_011517178.1:p.Thr84AlafsTer?
XM_005252105.3:c.499_500dup XP_005252162.1:p.Thr168AlafsTer?
XM_011518875.2:c.499_500dup XP_011517177.1:p.Thr168AlafsTer?
XM_011518876.2:c.247_248dup XP_011517178.1:p.Thr84AlafsTer?
XM_024447614.1:c.247_248dup XP_024303382.1:p.Thr84AlafsTer?
XM_024447615.1:c.247_248dup XP_024303383.1:p.Thr84AlafsTer?
NM_000962.4:c.574_575dup MANE Select NP_000953.2:p.Thr193AlafsTer?
NM_001271164.2:c.430_431dup NP_001258093.1:p.Thr145AlafsTer?
NM_001271165.2:c.247_248dup NP_001258094.1:p.Thr84AlafsTer?
NM_001271166.2:c.247_248dup NP_001258095.1:p.Thr84AlafsTer?
NM_001271367.2:c.247_248dup NP_001258296.1:p.Thr84AlafsTer?
NM_001271368.2:c.499_500dup NP_001258297.1:p.Thr168AlafsTer?
NM_080591.3:c.574_575dup NP_542158.1:p.Thr193AlafsTer?