Canonical Allele Identifier: CA377641677
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298390G>T , CM000672.2:g.94298390G>T GRCh38
NC_000010.10:g.96058147G>T , CM000672.1:g.96058147G>T GRCh37
NC_000010.9:g.96048137G>T NCBI36
NG_015799.1:g.309402G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4255G>T ENSP00000360426.1:p.Gly1419Cys
ENST00000685253.1:c.*1722G>T ENSP00000509405.1:n.*1722G>T
ENST00000685889.1:n.1914G>T
ENST00000686807.1:n.598G>T
ENST00000686954.1:c.*463G>T ENSP00000508416.1:n.*463G>T
ENST00000688810.1:c.4207G>T ENSP00000509140.1:p.Gly1403Cys
ENST00000689233.1:n.9387G>T
ENST00000690340.1:n.2852G>T
ENST00000692286.1:c.5047G>T ENSP00000509490.1:p.Gly1683Cys
ENST00000692396.1:c.5131G>T ENSP00000508605.1:p.Gly1711Cys
ENST00000371380.8:c.5179G>T MANE Select ENSP00000360431.2:p.Gly1727Cys
ENST00000371385.8:c.4153G>T ENSP00000360438.4:p.Gly1385Cys
ENST00000674738.1:c.3734G>T
ENST00000674827.1:c.3295G>T ENSP00000502523.1:p.Gly1099Cys
ENST00000675218.1:c.4255G>T ENSP00000501910.1:p.Gly1419Cys
ENST00000675487.1:c.*1112G>T ENSP00000502340.1:n.*1112G>T
ENST00000675718.1:c.4448G>T
ENST00000676102.1:c.4024G>T ENSP00000502811.1:p.Gly1342Cys
ENST00000260766.7:c.5179G>T ENSP00000260766.3:p.Gly1727Cys
ENST00000371375.1:c.4255G>T ENSP00000360426.1:p.Gly1419Cys
ENST00000371380.7:c.5179G>T ENSP00000360431.2:p.Gly1727Cys
ENST00000371385.7:c.4255G>T ENSP00000360438.3:p.Gly1419Cys
NM_001165979.2:c.4255G>T NP_001159451.1:p.Gly1419Cys
NM_001288989.1:c.5131G>T NP_001275918.1:p.Gly1711Cys
NM_016341.3:c.5179G>T NP_057425.3:p.Gly1727Cys
XM_006717885.2:c.5221G>T XP_006717948.1:p.Gly1741Cys
XM_006717886.2:c.5221G>T XP_006717949.1:p.Gly1741Cys
XM_006717888.2:c.5218G>T XP_006717951.1:p.Gly1740Cys
XM_006717889.2:c.5173G>T XP_006717952.1:p.Gly1725Cys
XM_006717890.1:c.4297G>T XP_006717953.1:p.Gly1433Cys
XM_011539849.1:c.5221G>T XP_011538151.1:p.Gly1741Cys
XM_011539850.1:c.4066G>T XP_011538152.1:p.Gly1356Cys
XM_006717885.4:c.5221G>T XP_006717948.1:p.Gly1741Cys
XM_006717888.4:c.5218G>T XP_006717951.1:p.Gly1740Cys
XM_006717889.4:c.5173G>T XP_006717952.1:p.Gly1725Cys
XM_006717890.3:c.4297G>T XP_006717953.1:p.Gly1433Cys
XM_011539849.3:c.5221G>T XP_011538151.1:p.Gly1741Cys
XM_011539850.3:c.4066G>T XP_011538152.1:p.Gly1356Cys
XM_017016310.2:c.5221G>T XP_016871799.1:p.Gly1741Cys
XM_017016311.2:c.5221G>T XP_016871800.1:p.Gly1741Cys
XM_017016312.2:c.4207G>T XP_016871801.1:p.Gly1403Cys
NM_001288989.2:c.5131G>T NP_001275918.1:p.Gly1711Cys
NM_016341.4:c.5179G>T MANE Select NP_057425.3:p.Gly1727Cys