Canonical Allele Identifier: CA377642074
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298577C>T , CM000672.2:g.94298577C>T GRCh38
NC_000010.10:g.96058334C>T , CM000672.1:g.96058334C>T GRCh37
NC_000010.9:g.96048324C>T NCBI36
NG_015799.1:g.309589C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:n.4442C>T ENSP00000360426.1:p.Pro1481Leu
ENST00000685253.1:c.*1909C>T ENSP00000509405.1:n.*1909C>T
ENST00000685889.1:n.2101C>T
ENST00000686807.1:n.785C>T
ENST00000686954.1:c.*650C>T ENSP00000508416.1:n.*650C>T
ENST00000688810.1:n.4394C>T ENSP00000509140.1:p.Pro1465Leu
ENST00000689233.1:n.9574C>T
ENST00000690340.1:n.3039C>T
ENST00000692286.1:c.5234C>T ENSP00000509490.1:p.Pro1745Leu
ENST00000692396.1:c.5318C>T ENSP00000508605.1:p.Pro1773Leu
ENST00000371380.8:c.5366C>T MANE Select ENSP00000360431.2:p.Pro1789Leu
ENST00000371385.8:c.4340C>T ENSP00000360438.4:p.Pro1447Leu
ENST00000674738.1:n.3921C>T
ENST00000674827.1:n.3482C>T ENSP00000502523.1:p.Pro1161Leu
ENST00000675218.1:n.4442C>T ENSP00000501910.1:p.Pro1481Leu
ENST00000675487.1:c.*1299C>T ENSP00000502340.1:n.*1299C>T
ENST00000675718.1:n.4635C>T
ENST00000260766.7:c.5366C>T ENSP00000260766.3:p.Pro1789Leu
ENST00000371375.1:n.4442C>T ENSP00000360426.1:p.Pro1481Leu
ENST00000371380.7:c.5366C>T ENSP00000360431.2:p.Pro1789Leu
ENST00000371385.7:c.4442C>T ENSP00000360438.3:p.Pro1481Leu
NM_001165979.2:c.4442C>T NP_001159451.1:p.Pro1481Leu
NM_001288989.1:c.5318C>T NP_001275918.1:p.Pro1773Leu
NM_016341.3:c.5366C>T NP_057425.3:p.Pro1789Leu
XM_006717885.2:c.5408C>T XP_006717948.1:p.Pro1803Leu
XM_006717886.2:c.5408C>T XP_006717949.1:p.Pro1803Leu
XM_006717888.2:c.5405C>T XP_006717951.1:p.Pro1802Leu
XM_006717889.2:c.5360C>T XP_006717952.1:p.Pro1787Leu
XM_006717890.1:c.4484C>T XP_006717953.1:p.Pro1495Leu
XM_011539849.1:c.5408C>T XP_011538151.1:p.Pro1803Leu
XM_011539850.1:c.4253C>T XP_011538152.1:p.Pro1418Leu
XM_006717885.4:c.5408C>T XP_006717948.1:p.Pro1803Leu
XM_006717888.4:c.5405C>T XP_006717951.1:p.Pro1802Leu
XM_006717889.4:c.5360C>T XP_006717952.1:p.Pro1787Leu
XM_006717890.3:c.4484C>T XP_006717953.1:p.Pro1495Leu
XM_011539849.3:c.5408C>T XP_011538151.1:p.Pro1803Leu
XM_011539850.3:c.4253C>T XP_011538152.1:p.Pro1418Leu
XM_017016310.2:c.5408C>T XP_016871799.1:p.Pro1803Leu
XM_017016311.2:c.5408C>T XP_016871800.1:p.Pro1803Leu
XM_017016312.2:c.4394C>T XP_016871801.1:p.Pro1465Leu
NM_001288989.2:c.5318C>T NP_001275918.1:p.Pro1773Leu
NM_016341.4:c.5366C>T MANE Select NP_057425.3:p.Pro1789Leu