Canonical Allele Identifier: CA377641861
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298477C>T , CM000672.2:g.94298477C>T GRCh38
NC_000010.10:g.96058234C>T , CM000672.1:g.96058234C>T GRCh37
NC_000010.9:g.96048224C>T NCBI36
NG_015799.1:g.309489C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5266C>T MANE Select ENSP00000360431.2:p.His1756Tyr
ENST00000371385.8:c.4240C>T ENSP00000360438.4:p.His1414Tyr
ENST00000674738.1:n.3821C>T
ENST00000674827.1:n.3382C>T ENSP00000502523.1:p.His1128Tyr
ENST00000675218.1:n.4342C>T ENSP00000501910.1:p.His1448Tyr
ENST00000675487.1:c.*1199C>T ENSP00000502340.1:p.=
ENST00000675718.1:n.4535C>T
ENST00000676102.1:c.4111C>T ENSP00000502811.1:p.Pro1371SerfsTer21
ENST00000260766.7:c.5266C>T ENSP00000260766.3:p.His1756Tyr
ENST00000371375.1:n.4342C>T ENSP00000360426.1:p.His1448Tyr
ENST00000371380.7:c.5266C>T ENSP00000360431.2:p.His1756Tyr
ENST00000371385.7:c.4342C>T ENSP00000360438.3:p.His1448Tyr
NM_001165979.2:c.4342C>T NP_001159451.1:p.His1448Tyr
NM_001288989.1:c.5218C>T NP_001275918.1:p.His1740Tyr
NM_016341.3:c.5266C>T NP_057425.3:p.His1756Tyr
XM_006717885.2:c.5308C>T XP_006717948.1:p.His1770Tyr
XM_006717886.2:c.5308C>T XP_006717949.1:p.His1770Tyr
XM_006717888.2:c.5305C>T XP_006717951.1:p.His1769Tyr
XM_006717889.2:c.5260C>T XP_006717952.1:p.His1754Tyr
XM_006717890.1:c.4384C>T XP_006717953.1:p.His1462Tyr
XM_011539849.1:c.5308C>T XP_011538151.1:p.His1770Tyr
XM_011539850.1:c.4153C>T XP_011538152.1:p.His1385Tyr
XM_006717885.4:c.5308C>T XP_006717948.1:p.His1770Tyr
XM_006717888.4:c.5305C>T XP_006717951.1:p.His1769Tyr
XM_006717889.4:c.5260C>T XP_006717952.1:p.His1754Tyr
XM_006717890.3:c.4384C>T XP_006717953.1:p.His1462Tyr
XM_011539849.3:c.5308C>T XP_011538151.1:p.His1770Tyr
XM_011539850.3:c.4153C>T XP_011538152.1:p.His1385Tyr
XM_017016310.2:c.5308C>T XP_016871799.1:p.His1770Tyr
XM_017016311.2:c.5308C>T XP_016871800.1:p.His1770Tyr
XM_017016312.2:c.4294C>T XP_016871801.1:p.His1432Tyr
NM_001288989.2:c.5218C>T NP_001275918.1:p.His1740Tyr
NM_016341.4:c.5266C>T MANE Select NP_057425.3:p.His1756Tyr