Canonical Allele Identifier: CA1880122202
Community Standard Title: NM_025072.7(PTGES2):c.893G= (p.Arg298=)
Gene: PTGES2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128122474C= , CM000671.2:g.128122474C= GRCh38
NC_000009.11:g.130884753C= , CM000671.1:g.130884753C= GRCh37
NC_000009.10:g.129924574C= NCBI36
NG_012488.1:g.10722G=

Transcript Alleles

HGVS Amino-acid Change
NM_025072.7:c.893G= MANE Select NP_079348.1:p.Arg298=
ENST00000338961.11:c.893G= MANE Select ENSP00000345341.6:p.Arg298=
NM_001256335.1:c.320G= NP_001243264.1:p.Arg107=
NM_001256335.2:c.320G= NP_001243264.1:p.Arg107=
NM_025072.6:c.893G= NP_079348.1:p.Arg298=
NM_198938.2:c.320G= NP_945176.1:p.Arg107=
NM_198938.3:c.320G= NP_945176.1:p.Arg107=
ENST00000277462.9:c.320G= ENSP00000277462.5:p.Arg107=
ENST00000338961.10:c.893G= ENSP00000345341.6:p.Arg298=
ENST00000449878.1:c.788G= ENSP00000411378.1:p.Arg263=
ENST00000474124.5:n.847G=
ENST00000474124.6:c.*316G= ENSP00000503197.1:n.*316G=
ENST00000476655.5:n.428G=
ENST00000476655.6:n.1590G=
ENST00000483625.6:n.1365G=
ENST00000487063.5:n.610G=
ENST00000493205.5:n.880G=
ENST00000493205.6:n.2803G=
ENST00000496594.5:n.1440G=
ENST00000497109.6:n.1358G=
ENST00000617202.4:c.320G= ENSP00000482913.1:p.Arg107=
ENST00000676562.1:c.*477G= ENSP00000504019.1:n.*477G=
ENST00000677651.1:c.*494G= ENSP00000502881.1:n.*494G=
ENST00000677691.1:c.320G= ENSP00000503821.1:p.Arg107=
ENST00000677980.1:c.*940G= ENSP00000503843.1:n.*940G=
ENST00000678174.1:c.869G= ENSP00000504703.1:p.Arg290=
ENST00000678916.1:c.*127G= ENSP00000504746.1:n.*127G=
ENST00000679345.1:c.*657G= ENSP00000502870.1:n.*657G=
XM_005252239.1:c.320G= XP_005252296.1:p.Arg107=
XM_005252239.2:c.320G= XP_005252296.1:p.Arg107=
XM_011519050.1:c.320G= XP_011517352.1:p.Arg107=
XM_011519051.1:c.320G= XP_011517353.1:p.Arg107=
XM_011519051.3:c.320G= XP_011517353.1:p.Arg107=
XM_024447688.1:c.320G= XP_024303456.1:p.Arg107=
XR_001746383.2:n.1299G=