Canonical Allele Identifier: CA377641673
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4254A>C ENSP00000360426.1:p.Glu1418Asp
ENST00000685253.1:c.*1721A>C ENSP00000509405.1:n.*1721A>C
ENST00000685889.1:n.1913A>C
ENST00000686807.1:n.597A>C
ENST00000686954.1:c.*462A>C ENSP00000508416.1:n.*462A>C
ENST00000688810.1:c.4206A>C ENSP00000509140.1:p.Glu1402Asp
ENST00000689233.1:n.9386A>C
ENST00000690340.1:n.2851A>C
ENST00000692286.1:c.5046A>C ENSP00000509490.1:p.Glu1682Asp
ENST00000692396.1:c.5130A>C ENSP00000508605.1:p.Glu1710Asp
ENST00000371380.8:c.5178A>C MANE Select ENSP00000360431.2:p.Glu1726Asp
ENST00000371385.8:c.4152A>C ENSP00000360438.4:p.Glu1384Asp
ENST00000674738.1:c.3733A>C
ENST00000674827.1:c.3294A>C ENSP00000502523.1:p.Glu1098Asp
ENST00000675218.1:c.4254A>C ENSP00000501910.1:p.Glu1418Asp
ENST00000675487.1:c.*1111A>C ENSP00000502340.1:n.*1111A>C
ENST00000675718.1:c.4447A>C
ENST00000676102.1:c.4023A>C ENSP00000502811.1:p.Glu1341Asp
ENST00000260766.7:c.5178A>C ENSP00000260766.3:p.Glu1726Asp
ENST00000371375.1:c.4254A>C ENSP00000360426.1:p.Glu1418Asp
ENST00000371380.7:c.5178A>C ENSP00000360431.2:p.Glu1726Asp
ENST00000371385.7:c.4254A>C ENSP00000360438.3:p.Glu1418Asp
NM_001165979.2:c.4254A>C NP_001159451.1:p.Glu1418Asp
NM_001288989.1:c.5130A>C NP_001275918.1:p.Glu1710Asp
NM_016341.3:c.5178A>C NP_057425.3:p.Glu1726Asp
XM_006717885.2:c.5220A>C XP_006717948.1:p.Glu1740Asp
XM_006717886.2:c.5220A>C XP_006717949.1:p.Glu1740Asp
XM_006717888.2:c.5217A>C XP_006717951.1:p.Glu1739Asp
XM_006717889.2:c.5172A>C XP_006717952.1:p.Glu1724Asp
XM_006717890.1:c.4296A>C XP_006717953.1:p.Glu1432Asp
XM_011539849.1:c.5220A>C XP_011538151.1:p.Glu1740Asp
XM_011539850.1:c.4065A>C XP_011538152.1:p.Glu1355Asp
XM_006717885.4:c.5220A>C XP_006717948.1:p.Glu1740Asp
XM_006717888.4:c.5217A>C XP_006717951.1:p.Glu1739Asp
XM_006717889.4:c.5172A>C XP_006717952.1:p.Glu1724Asp
XM_006717890.3:c.4296A>C XP_006717953.1:p.Glu1432Asp
XM_011539849.3:c.5220A>C XP_011538151.1:p.Glu1740Asp
XM_011539850.3:c.4065A>C XP_011538152.1:p.Glu1355Asp
XM_017016310.2:c.5220A>C XP_016871799.1:p.Glu1740Asp
XM_017016311.2:c.5220A>C XP_016871800.1:p.Glu1740Asp
XM_017016312.2:c.4206A>C XP_016871801.1:p.Glu1402Asp
NM_001288989.2:c.5130A>C NP_001275918.1:p.Glu1710Asp
NM_016341.4:c.5178A>C MANE Select NP_057425.3:p.Glu1726Asp