Canonical Allele Identifier: CA1928998368
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298389A= , CM000672.2:g.94298389A= GRCh38
NC_000010.10:g.96058146A= , CM000672.1:g.96058146A= GRCh37
NC_000010.9:g.96048136A= NCBI36
NG_015799.1:g.309401A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:n.4254A= ENSP00000360426.1:p.Glu1418=
ENST00000685253.1:c.*1721A= ENSP00000509405.1:n.*1721A=
ENST00000685889.1:n.1913A=
ENST00000686807.1:n.597A=
ENST00000686954.1:c.*462A= ENSP00000508416.1:n.*462A=
ENST00000688810.1:n.4206A= ENSP00000509140.1:p.Glu1402=
ENST00000689233.1:n.9386A=
ENST00000690340.1:n.2851A=
ENST00000692286.1:c.5046A= ENSP00000509490.1:p.Glu1682=
ENST00000692396.1:c.5130A= ENSP00000508605.1:p.Glu1710=
ENST00000371380.8:c.5178A= MANE Select ENSP00000360431.2:p.Glu1726=
ENST00000371385.8:c.4152A= ENSP00000360438.4:p.Glu1384=
ENST00000674738.1:n.3733A=
ENST00000674827.1:n.3294A= ENSP00000502523.1:p.Glu1098=
ENST00000675218.1:n.4254A= ENSP00000501910.1:p.Glu1418=
ENST00000675487.1:c.*1111A= ENSP00000502340.1:n.*1111A=
ENST00000675718.1:n.4447A=
ENST00000676102.1:c.4023A= ENSP00000502811.1:p.Glu1341=
ENST00000260766.7:c.5178A= ENSP00000260766.3:p.Glu1726=
ENST00000371375.1:n.4254A= ENSP00000360426.1:p.Glu1418=
ENST00000371380.7:c.5178A= ENSP00000360431.2:p.Glu1726=
ENST00000371385.7:c.4254A= ENSP00000360438.3:p.Glu1418=
NM_001165979.2:c.4254A= NP_001159451.1:p.Glu1418=
NM_001288989.1:c.5130A= NP_001275918.1:p.Glu1710=
NM_016341.3:c.5178A= NP_057425.3:p.Glu1726=
XM_006717885.2:c.5220A= XP_006717948.1:p.Glu1740=
XM_006717886.2:c.5220A= XP_006717949.1:p.Glu1740=
XM_006717888.2:c.5217A= XP_006717951.1:p.Glu1739=
XM_006717889.2:c.5172A= XP_006717952.1:p.Glu1724=
XM_006717890.1:c.4296A= XP_006717953.1:p.Glu1432=
XM_011539849.1:c.5220A= XP_011538151.1:p.Glu1740=
XM_011539850.1:c.4065A= XP_011538152.1:p.Glu1355=
XM_006717885.4:c.5220A= XP_006717948.1:p.Glu1740=
XM_006717888.4:c.5217A= XP_006717951.1:p.Glu1739=
XM_006717889.4:c.5172A= XP_006717952.1:p.Glu1724=
XM_006717890.3:c.4296A= XP_006717953.1:p.Glu1432=
XM_011539849.3:c.5220A= XP_011538151.1:p.Glu1740=
XM_011539850.3:c.4065A= XP_011538152.1:p.Glu1355=
XM_017016310.2:c.5220A= XP_016871799.1:p.Glu1740=
XM_017016311.2:c.5220A= XP_016871800.1:p.Glu1740=
XM_017016312.2:c.4206A= XP_016871801.1:p.Glu1402=
NM_001288989.2:c.5130A= NP_001275918.1:p.Glu1710=
NM_016341.4:c.5178A= MANE Select NP_057425.3:p.Glu1726=