Canonical Allele Identifier: CA1877496576
Gene: PTGS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122381458T= , CM000671.2:g.122381458T= GRCh38
NC_000009.11:g.125143737T= , CM000671.1:g.125143737T= GRCh37
NC_000009.10:g.124183558T= NCBI36
NG_032900.1:g.15509T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362012.7:c.584T= MANE Select ENSP00000354612.2:p.Leu195=
ENST00000373698.7:c.257T= ENSP00000362802.5:p.Leu86=
ENST00000426608.6:c.313-38T= ENSP00000411606.2:n.313-38T=
ENST00000540753.6:c.509T= ENSP00000437709.1:p.Leu170=
ENST00000619306.5:c.440T= ENSP00000483540.2:p.Leu147=
ENST00000643576.1:n.678T=
ENST00000643810.1:c.257T= ENSP00000494717.1:p.Leu86=
ENST00000645132.1:n.519+2885T=
ENST00000647067.1:c.*429T= ENSP00000495728.1:n.*429T=
ENST00000223423.8:c.584T= ENSP00000223423.4:p.Leu195=
ENST00000362012.6:c.584T= ENSP00000354612.2:p.Leu195=
ENST00000373698.6:c.257T= ENSP00000362802.5:p.Leu86=
ENST00000426608.5:c.304-38T= ENSP00000411606.1:n.304-38T=
ENST00000540753.5:c.509T= ENSP00000437709.1:p.Leu170=
ENST00000614910.4:c.440T= ENSP00000484800.1:p.Leu147=
ENST00000619306.4:c.677T= ENSP00000483540.1:p.Leu226=
NM_000962.3:c.584T= NP_000953.2:p.Leu195=
NM_001271164.1:c.440T= NP_001258093.1:p.Leu147=
NM_001271165.1:c.257T= NP_001258094.1:p.Leu86=
NM_001271166.1:c.257T= NP_001258095.1:p.Leu86=
NM_001271367.1:c.257T= NP_001258296.1:p.Leu86=
NM_001271368.1:c.509T= NP_001258297.1:p.Leu170=
NM_080591.2:c.584T= NP_542158.1:p.Leu195=
XM_005252105.2:c.509T= XP_005252162.1:p.Leu170=
XM_011518875.1:c.509T= XP_011517177.1:p.Leu170=
XM_011518876.1:c.257T= XP_011517178.1:p.Leu86=
XM_005252105.3:c.509T= XP_005252162.1:p.Leu170=
XM_011518875.2:c.509T= XP_011517177.1:p.Leu170=
XM_011518876.2:c.257T= XP_011517178.1:p.Leu86=
XM_024447614.1:c.257T= XP_024303382.1:p.Leu86=
XM_024447615.1:c.257T= XP_024303383.1:p.Leu86=
NM_000962.4:c.584T= MANE Select NP_000953.2:p.Leu195=
NM_001271164.2:c.440T= NP_001258093.1:p.Leu147=
NM_001271165.2:c.257T= NP_001258094.1:p.Leu86=
NM_001271166.2:c.257T= NP_001258095.1:p.Leu86=
NM_001271367.2:c.257T= NP_001258296.1:p.Leu86=
NM_001271368.2:c.509T= NP_001258297.1:p.Leu170=
NM_080591.3:c.584T= NP_542158.1:p.Leu195=