Canonical Allele Identifier: CA377642009
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298546C>T , CM000672.2:g.94298546C>T GRCh38
NC_000010.10:g.96058303C>T , CM000672.1:g.96058303C>T GRCh37
NC_000010.9:g.96048293C>T NCBI36
NG_015799.1:g.309558C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4411C>T ENSP00000360426.1:p.His1471Tyr
ENST00000685253.1:c.*1878C>T ENSP00000509405.1:n.*1878C>T
ENST00000685889.1:n.2070C>T
ENST00000686807.1:n.754C>T
ENST00000686954.1:c.*619C>T ENSP00000508416.1:n.*619C>T
ENST00000688810.1:c.4363C>T ENSP00000509140.1:p.His1455Tyr
ENST00000689233.1:n.9543C>T
ENST00000690340.1:n.3008C>T
ENST00000692286.1:c.5203C>T ENSP00000509490.1:p.His1735Tyr
ENST00000692396.1:c.5287C>T ENSP00000508605.1:p.His1763Tyr
ENST00000371380.8:c.5335C>T MANE Select ENSP00000360431.2:p.His1779Tyr
ENST00000371385.8:c.4309C>T ENSP00000360438.4:p.His1437Tyr
ENST00000674738.1:c.3890C>T
ENST00000674827.1:c.3451C>T ENSP00000502523.1:p.His1151Tyr
ENST00000675218.1:c.4411C>T ENSP00000501910.1:p.His1471Tyr
ENST00000675487.1:c.*1268C>T ENSP00000502340.1:n.*1268C>T
ENST00000675718.1:c.4604C>T
ENST00000260766.7:c.5335C>T ENSP00000260766.3:p.His1779Tyr
ENST00000371375.1:c.4411C>T ENSP00000360426.1:p.His1471Tyr
ENST00000371380.7:c.5335C>T ENSP00000360431.2:p.His1779Tyr
ENST00000371385.7:c.4411C>T ENSP00000360438.3:p.His1471Tyr
NM_001165979.2:c.4411C>T NP_001159451.1:p.His1471Tyr
NM_001288989.1:c.5287C>T NP_001275918.1:p.His1763Tyr
NM_016341.3:c.5335C>T NP_057425.3:p.His1779Tyr
XM_006717885.2:c.5377C>T XP_006717948.1:p.His1793Tyr
XM_006717886.2:c.5377C>T XP_006717949.1:p.His1793Tyr
XM_006717888.2:c.5374C>T XP_006717951.1:p.His1792Tyr
XM_006717889.2:c.5329C>T XP_006717952.1:p.His1777Tyr
XM_006717890.1:c.4453C>T XP_006717953.1:p.His1485Tyr
XM_011539849.1:c.5377C>T XP_011538151.1:p.His1793Tyr
XM_011539850.1:c.4222C>T XP_011538152.1:p.His1408Tyr
XM_006717885.4:c.5377C>T XP_006717948.1:p.His1793Tyr
XM_006717888.4:c.5374C>T XP_006717951.1:p.His1792Tyr
XM_006717889.4:c.5329C>T XP_006717952.1:p.His1777Tyr
XM_006717890.3:c.4453C>T XP_006717953.1:p.His1485Tyr
XM_011539849.3:c.5377C>T XP_011538151.1:p.His1793Tyr
XM_011539850.3:c.4222C>T XP_011538152.1:p.His1408Tyr
XM_017016310.2:c.5377C>T XP_016871799.1:p.His1793Tyr
XM_017016311.2:c.5377C>T XP_016871800.1:p.His1793Tyr
XM_017016312.2:c.4363C>T XP_016871801.1:p.His1455Tyr
NM_001288989.2:c.5287C>T NP_001275918.1:p.His1763Tyr
NM_016341.4:c.5335C>T MANE Select NP_057425.3:p.His1779Tyr