Canonical Allele Identifier: CA1928998439
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298560G= , CM000672.2:g.94298560G= GRCh38
NC_000010.10:g.96058317G= , CM000672.1:g.96058317G= GRCh37
NC_000010.9:g.96048307G= NCBI36
NG_015799.1:g.309572G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5349G= MANE Select ENSP00000360431.2:p.Gln1783=
ENST00000371385.8:c.4323G= ENSP00000360438.4:p.Gln1441=
ENST00000674738.1:n.3904G=
ENST00000674827.1:n.3465G= ENSP00000502523.1:p.Gln1155=
ENST00000675218.1:n.4425G= ENSP00000501910.1:p.Gln1475=
ENST00000675487.1:c.*1282G= ENSP00000502340.1:p.=
ENST00000675718.1:n.4618G=
ENST00000260766.7:c.5349G= ENSP00000260766.3:p.Gln1783=
ENST00000371375.1:n.4425G= ENSP00000360426.1:p.Gln1475=
ENST00000371380.7:c.5349G= ENSP00000360431.2:p.Gln1783=
ENST00000371385.7:c.4425G= ENSP00000360438.3:p.Gln1475=
NM_001165979.2:c.4425G= NP_001159451.1:p.Gln1475=
NM_001288989.1:c.5301G= NP_001275918.1:p.Gln1767=
NM_016341.3:c.5349G= NP_057425.3:p.Gln1783=
XM_006717885.2:c.5391G= XP_006717948.1:p.Gln1797=
XM_006717886.2:c.5391G= XP_006717949.1:p.Gln1797=
XM_006717888.2:c.5388G= XP_006717951.1:p.Gln1796=
XM_006717889.2:c.5343G= XP_006717952.1:p.Gln1781=
XM_006717890.1:c.4467G= XP_006717953.1:p.Gln1489=
XM_011539849.1:c.5391G= XP_011538151.1:p.Gln1797=
XM_011539850.1:c.4236G= XP_011538152.1:p.Gln1412=
XM_006717885.4:c.5391G= XP_006717948.1:p.Gln1797=
XM_006717888.4:c.5388G= XP_006717951.1:p.Gln1796=
XM_006717889.4:c.5343G= XP_006717952.1:p.Gln1781=
XM_006717890.3:c.4467G= XP_006717953.1:p.Gln1489=
XM_011539849.3:c.5391G= XP_011538151.1:p.Gln1797=
XM_011539850.3:c.4236G= XP_011538152.1:p.Gln1412=
XM_017016310.2:c.5391G= XP_016871799.1:p.Gln1797=
XM_017016311.2:c.5391G= XP_016871800.1:p.Gln1797=
XM_017016312.2:c.4377G= XP_016871801.1:p.Gln1459=
NM_001288989.2:c.5301G= NP_001275918.1:p.Gln1767=
NM_016341.4:c.5349G= MANE Select NP_057425.3:p.Gln1783=