Canonical Allele Identifier: CA377642027
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298555T>C , CM000672.2:g.94298555T>C GRCh38
NC_000010.10:g.96058312T>C , CM000672.1:g.96058312T>C GRCh37
NC_000010.9:g.96048302T>C NCBI36
NG_015799.1:g.309567T>C

Transcript Alleles

HGVS Amino-acid change
NM_001165979.2:c.4420T>C NP_001159451.1:p.Cys1474Arg
NM_001288989.1:c.5296T>C NP_001275918.1:p.Cys1766Arg
NM_016341.3:c.5344T>C NP_057425.3:p.Cys1782Arg
XM_006717885.2:c.5386T>C XP_006717948.1:p.Cys1796Arg
XM_006717886.2:c.5386T>C XP_006717949.1:p.Cys1796Arg
XM_006717888.2:c.5383T>C XP_006717951.1:p.Cys1795Arg
XM_006717889.2:c.5338T>C XP_006717952.1:p.Cys1780Arg
XM_006717890.1:c.4462T>C XP_006717953.1:p.Cys1488Arg
XM_011539849.1:c.5386T>C XP_011538151.1:p.Cys1796Arg
XM_011539850.1:c.4231T>C XP_011538152.1:p.Cys1411Arg
XM_006717885.4:c.5386T>C XP_006717948.1:p.Cys1796Arg
XM_006717888.4:c.5383T>C XP_006717951.1:p.Cys1795Arg
XM_006717889.4:c.5338T>C XP_006717952.1:p.Cys1780Arg
XM_006717890.3:c.4462T>C XP_006717953.1:p.Cys1488Arg
XM_011539849.3:c.5386T>C XP_011538151.1:p.Cys1796Arg
XM_011539850.3:c.4231T>C XP_011538152.1:p.Cys1411Arg
XM_017016310.2:c.5386T>C XP_016871799.1:p.Cys1796Arg
XM_017016311.2:c.5386T>C XP_016871800.1:p.Cys1796Arg
XM_017016312.2:c.4372T>C XP_016871801.1:p.Cys1458Arg
NM_001288989.2:c.5296T>C NP_001275918.1:p.Cys1766Arg
NM_016341.4:c.5344T>C MANE Select NP_057425.3:p.Cys1782Arg
ENST00000260766.7:c.5344T>C ENSP00000260766.3:p.Cys1782Arg
ENST00000371375.1:n.4420T>C ENSP00000360426.1:p.Cys1474Arg
ENST00000371380.7:c.5344T>C ENSP00000360431.2:p.Cys1782Arg
ENST00000371385.7:c.4420T>C ENSP00000360438.3:p.Cys1474Arg