Canonical Allele Identifier: CA1928998403
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298463C= , CM000672.2:g.94298463C= GRCh38
NC_000010.10:g.96058220C= , CM000672.1:g.96058220C= GRCh37
NC_000010.9:g.96048210C= NCBI36
NG_015799.1:g.309475C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5252C= MANE Select ENSP00000360431.2:p.Thr1751=
ENST00000371385.8:c.4226C= ENSP00000360438.4:p.Thr1409=
ENST00000674738.1:n.3807C=
ENST00000674827.1:n.3368C= ENSP00000502523.1:p.Thr1123=
ENST00000675218.1:n.4328C= ENSP00000501910.1:p.Thr1443=
ENST00000675487.1:c.*1185C= ENSP00000502340.1:p.=
ENST00000675718.1:n.4521C=
ENST00000676102.1:c.4097C= ENSP00000502811.1:p.Thr1366=
ENST00000260766.7:c.5252C= ENSP00000260766.3:p.Thr1751=
ENST00000371375.1:n.4328C= ENSP00000360426.1:p.Thr1443=
ENST00000371380.7:c.5252C= ENSP00000360431.2:p.Thr1751=
ENST00000371385.7:c.4328C= ENSP00000360438.3:p.Thr1443=
NM_001165979.2:c.4328C= NP_001159451.1:p.Thr1443=
NM_001288989.1:c.5204C= NP_001275918.1:p.Thr1735=
NM_016341.3:c.5252C= NP_057425.3:p.Thr1751=
XM_006717885.2:c.5294C= XP_006717948.1:p.Thr1765=
XM_006717886.2:c.5294C= XP_006717949.1:p.Thr1765=
XM_006717888.2:c.5291C= XP_006717951.1:p.Thr1764=
XM_006717889.2:c.5246C= XP_006717952.1:p.Thr1749=
XM_006717890.1:c.4370C= XP_006717953.1:p.Thr1457=
XM_011539849.1:c.5294C= XP_011538151.1:p.Thr1765=
XM_011539850.1:c.4139C= XP_011538152.1:p.Thr1380=
XM_006717885.4:c.5294C= XP_006717948.1:p.Thr1765=
XM_006717888.4:c.5291C= XP_006717951.1:p.Thr1764=
XM_006717889.4:c.5246C= XP_006717952.1:p.Thr1749=
XM_006717890.3:c.4370C= XP_006717953.1:p.Thr1457=
XM_011539849.3:c.5294C= XP_011538151.1:p.Thr1765=
XM_011539850.3:c.4139C= XP_011538152.1:p.Thr1380=
XM_017016310.2:c.5294C= XP_016871799.1:p.Thr1765=
XM_017016311.2:c.5294C= XP_016871800.1:p.Thr1765=
XM_017016312.2:c.4280C= XP_016871801.1:p.Thr1427=
NM_001288989.2:c.5204C= NP_001275918.1:p.Thr1735=
NM_016341.4:c.5252C= MANE Select NP_057425.3:p.Thr1751=