Canonical Allele Identifier: CA1928998409
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298479T= , CM000672.2:g.94298479T= GRCh38
NC_000010.10:g.96058236T= , CM000672.1:g.96058236T= GRCh37
NC_000010.9:g.96048226T= NCBI36
NG_015799.1:g.309491T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4344T= ENSP00000360426.1:p.His1448=
ENST00000685253.1:c.*1811T= ENSP00000509405.1:n.*1811T=
ENST00000685889.1:n.2003T=
ENST00000686807.1:n.687T=
ENST00000686954.1:c.*552T= ENSP00000508416.1:n.*552T=
ENST00000688810.1:c.4296T= ENSP00000509140.1:p.His1432=
ENST00000689233.1:n.9476T=
ENST00000690340.1:n.2941T=
ENST00000692286.1:c.5136T= ENSP00000509490.1:p.His1712=
ENST00000692396.1:c.5220T= ENSP00000508605.1:p.His1740=
ENST00000371380.8:c.5268T= MANE Select ENSP00000360431.2:p.His1756=
ENST00000371385.8:c.4242T= ENSP00000360438.4:p.His1414=
ENST00000674738.1:c.3823T=
ENST00000674827.1:c.3384T= ENSP00000502523.1:p.His1128=
ENST00000675218.1:c.4344T= ENSP00000501910.1:p.His1448=
ENST00000675487.1:c.*1201T= ENSP00000502340.1:n.*1201T=
ENST00000675718.1:c.4537T=
ENST00000260766.7:c.5268T= ENSP00000260766.3:p.His1756=
ENST00000371375.1:c.4344T= ENSP00000360426.1:p.His1448=
ENST00000371380.7:c.5268T= ENSP00000360431.2:p.His1756=
ENST00000371385.7:c.4344T= ENSP00000360438.3:p.His1448=
NM_001165979.2:c.4344T= NP_001159451.1:p.His1448=
NM_001288989.1:c.5220T= NP_001275918.1:p.His1740=
NM_016341.3:c.5268T= NP_057425.3:p.His1756=
XM_006717885.2:c.5310T= XP_006717948.1:p.His1770=
XM_006717886.2:c.5310T= XP_006717949.1:p.His1770=
XM_006717888.2:c.5307T= XP_006717951.1:p.His1769=
XM_006717889.2:c.5262T= XP_006717952.1:p.His1754=
XM_006717890.1:c.4386T= XP_006717953.1:p.His1462=
XM_011539849.1:c.5310T= XP_011538151.1:p.His1770=
XM_011539850.1:c.4155T= XP_011538152.1:p.His1385=
XM_006717885.4:c.5310T= XP_006717948.1:p.His1770=
XM_006717888.4:c.5307T= XP_006717951.1:p.His1769=
XM_006717889.4:c.5262T= XP_006717952.1:p.His1754=
XM_006717890.3:c.4386T= XP_006717953.1:p.His1462=
XM_011539849.3:c.5310T= XP_011538151.1:p.His1770=
XM_011539850.3:c.4155T= XP_011538152.1:p.His1385=
XM_017016310.2:c.5310T= XP_016871799.1:p.His1770=
XM_017016311.2:c.5310T= XP_016871800.1:p.His1770=
XM_017016312.2:c.4296T= XP_016871801.1:p.His1432=
NM_001288989.2:c.5220T= NP_001275918.1:p.His1740=
NM_016341.4:c.5268T= MANE Select NP_057425.3:p.His1756=