Canonical Allele Identifier: CA1928998437
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298553C= , CM000672.2:g.94298553C= GRCh38
NC_000010.10:g.96058310C= , CM000672.1:g.96058310C= GRCh37
NC_000010.9:g.96048300C= NCBI36
NG_015799.1:g.309565C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4418C= ENSP00000360426.1:p.Ala1473=
ENST00000685253.1:c.*1885C= ENSP00000509405.1:n.*1885C=
ENST00000685889.1:n.2077C=
ENST00000686807.1:n.761C=
ENST00000686954.1:c.*626C= ENSP00000508416.1:n.*626C=
ENST00000688810.1:c.4370C= ENSP00000509140.1:p.Ala1457=
ENST00000689233.1:n.9550C=
ENST00000690340.1:n.3015C=
ENST00000692286.1:c.5210C= ENSP00000509490.1:p.Ala1737=
ENST00000692396.1:c.5294C= ENSP00000508605.1:p.Ala1765=
ENST00000371380.8:c.5342C= MANE Select ENSP00000360431.2:p.Ala1781=
ENST00000371385.8:c.4316C= ENSP00000360438.4:p.Ala1439=
ENST00000674738.1:c.3897C=
ENST00000674827.1:c.3458C= ENSP00000502523.1:p.Ala1153=
ENST00000675218.1:c.4418C= ENSP00000501910.1:p.Ala1473=
ENST00000675487.1:c.*1275C= ENSP00000502340.1:n.*1275C=
ENST00000675718.1:c.4611C=
ENST00000260766.7:c.5342C= ENSP00000260766.3:p.Ala1781=
ENST00000371375.1:c.4418C= ENSP00000360426.1:p.Ala1473=
ENST00000371380.7:c.5342C= ENSP00000360431.2:p.Ala1781=
ENST00000371385.7:c.4418C= ENSP00000360438.3:p.Ala1473=
NM_001165979.2:c.4418C= NP_001159451.1:p.Ala1473=
NM_001288989.1:c.5294C= NP_001275918.1:p.Ala1765=
NM_016341.3:c.5342C= NP_057425.3:p.Ala1781=
XM_006717885.2:c.5384C= XP_006717948.1:p.Ala1795=
XM_006717886.2:c.5384C= XP_006717949.1:p.Ala1795=
XM_006717888.2:c.5381C= XP_006717951.1:p.Ala1794=
XM_006717889.2:c.5336C= XP_006717952.1:p.Ala1779=
XM_006717890.1:c.4460C= XP_006717953.1:p.Ala1487=
XM_011539849.1:c.5384C= XP_011538151.1:p.Ala1795=
XM_011539850.1:c.4229C= XP_011538152.1:p.Ala1410=
XM_006717885.4:c.5384C= XP_006717948.1:p.Ala1795=
XM_006717888.4:c.5381C= XP_006717951.1:p.Ala1794=
XM_006717889.4:c.5336C= XP_006717952.1:p.Ala1779=
XM_006717890.3:c.4460C= XP_006717953.1:p.Ala1487=
XM_011539849.3:c.5384C= XP_011538151.1:p.Ala1795=
XM_011539850.3:c.4229C= XP_011538152.1:p.Ala1410=
XM_017016310.2:c.5384C= XP_016871799.1:p.Ala1795=
XM_017016311.2:c.5384C= XP_016871800.1:p.Ala1795=
XM_017016312.2:c.4370C= XP_016871801.1:p.Ala1457=
NM_001288989.2:c.5294C= NP_001275918.1:p.Ala1765=
NM_016341.4:c.5342C= MANE Select NP_057425.3:p.Ala1781=