Canonical Allele Identifier: CA1928998397
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298442C= , CM000672.2:g.94298442C= GRCh38
NC_000010.10:g.96058199C= , CM000672.1:g.96058199C= GRCh37
NC_000010.9:g.96048189C= NCBI36
NG_015799.1:g.309454C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4307C= ENSP00000360426.1:p.Ser1436=
ENST00000685253.1:c.*1774C= ENSP00000509405.1:n.*1774C=
ENST00000685889.1:n.1966C=
ENST00000686807.1:n.650C=
ENST00000686954.1:c.*515C= ENSP00000508416.1:n.*515C=
ENST00000688810.1:c.4259C= ENSP00000509140.1:p.Ser1420=
ENST00000689233.1:n.9439C=
ENST00000690340.1:n.2904C=
ENST00000692286.1:c.5099C= ENSP00000509490.1:p.Ser1700=
ENST00000692396.1:c.5183C= ENSP00000508605.1:p.Ser1728=
ENST00000371380.8:c.5231C= MANE Select ENSP00000360431.2:p.Ser1744=
ENST00000371385.8:c.4205C= ENSP00000360438.4:p.Ser1402=
ENST00000674738.1:c.3786C=
ENST00000674827.1:c.3347C= ENSP00000502523.1:p.Ser1116=
ENST00000675218.1:c.4307C= ENSP00000501910.1:p.Ser1436=
ENST00000675487.1:c.*1164C= ENSP00000502340.1:n.*1164C=
ENST00000675718.1:c.4500C=
ENST00000676102.1:c.4076C= ENSP00000502811.1:p.Ser1359=
ENST00000260766.7:c.5231C= ENSP00000260766.3:p.Ser1744=
ENST00000371375.1:c.4307C= ENSP00000360426.1:p.Ser1436=
ENST00000371380.7:c.5231C= ENSP00000360431.2:p.Ser1744=
ENST00000371385.7:c.4307C= ENSP00000360438.3:p.Ser1436=
NM_001165979.2:c.4307C= NP_001159451.1:p.Ser1436=
NM_001288989.1:c.5183C= NP_001275918.1:p.Ser1728=
NM_016341.3:c.5231C= NP_057425.3:p.Ser1744=
XM_006717885.2:c.5273C= XP_006717948.1:p.Ser1758=
XM_006717886.2:c.5273C= XP_006717949.1:p.Ser1758=
XM_006717888.2:c.5270C= XP_006717951.1:p.Ser1757=
XM_006717889.2:c.5225C= XP_006717952.1:p.Ser1742=
XM_006717890.1:c.4349C= XP_006717953.1:p.Ser1450=
XM_011539849.1:c.5273C= XP_011538151.1:p.Ser1758=
XM_011539850.1:c.4118C= XP_011538152.1:p.Ser1373=
XM_006717885.4:c.5273C= XP_006717948.1:p.Ser1758=
XM_006717888.4:c.5270C= XP_006717951.1:p.Ser1757=
XM_006717889.4:c.5225C= XP_006717952.1:p.Ser1742=
XM_006717890.3:c.4349C= XP_006717953.1:p.Ser1450=
XM_011539849.3:c.5273C= XP_011538151.1:p.Ser1758=
XM_011539850.3:c.4118C= XP_011538152.1:p.Ser1373=
XM_017016310.2:c.5273C= XP_016871799.1:p.Ser1758=
XM_017016311.2:c.5273C= XP_016871800.1:p.Ser1758=
XM_017016312.2:c.4259C= XP_016871801.1:p.Ser1420=
NM_001288989.2:c.5183C= NP_001275918.1:p.Ser1728=
NM_016341.4:c.5231C= MANE Select NP_057425.3:p.Ser1744=