Canonical Allele Identifier: CA377642045
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298564C>A , CM000672.2:g.94298564C>A GRCh38
NC_000010.10:g.96058321C>A , CM000672.1:g.96058321C>A GRCh37
NC_000010.9:g.96048311C>A NCBI36
NG_015799.1:g.309576C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4429C>A ENSP00000360426.1:p.Leu1477Met
ENST00000685253.1:c.*1896C>A ENSP00000509405.1:n.*1896C>A
ENST00000685889.1:n.2088C>A
ENST00000686807.1:n.772C>A
ENST00000686954.1:c.*637C>A ENSP00000508416.1:n.*637C>A
ENST00000688810.1:c.4381C>A ENSP00000509140.1:p.Leu1461Met
ENST00000689233.1:n.9561C>A
ENST00000690340.1:n.3026C>A
ENST00000692286.1:c.5221C>A ENSP00000509490.1:p.Leu1741Met
ENST00000692396.1:c.5305C>A ENSP00000508605.1:p.Leu1769Met
ENST00000371380.8:c.5353C>A MANE Select ENSP00000360431.2:p.Leu1785Met
ENST00000371385.8:c.4327C>A ENSP00000360438.4:p.Leu1443Met
ENST00000674738.1:c.3908C>A
ENST00000674827.1:c.3469C>A ENSP00000502523.1:p.Leu1157Met
ENST00000675218.1:c.4429C>A ENSP00000501910.1:p.Leu1477Met
ENST00000675487.1:c.*1286C>A ENSP00000502340.1:n.*1286C>A
ENST00000675718.1:c.4622C>A
ENST00000260766.7:c.5353C>A ENSP00000260766.3:p.Leu1785Met
ENST00000371375.1:c.4429C>A ENSP00000360426.1:p.Leu1477Met
ENST00000371380.7:c.5353C>A ENSP00000360431.2:p.Leu1785Met
ENST00000371385.7:c.4429C>A ENSP00000360438.3:p.Leu1477Met
NM_001165979.2:c.4429C>A NP_001159451.1:p.Leu1477Met
NM_001288989.1:c.5305C>A NP_001275918.1:p.Leu1769Met
NM_016341.3:c.5353C>A NP_057425.3:p.Leu1785Met
XM_006717885.2:c.5395C>A XP_006717948.1:p.Leu1799Met
XM_006717886.2:c.5395C>A XP_006717949.1:p.Leu1799Met
XM_006717888.2:c.5392C>A XP_006717951.1:p.Leu1798Met
XM_006717889.2:c.5347C>A XP_006717952.1:p.Leu1783Met
XM_006717890.1:c.4471C>A XP_006717953.1:p.Leu1491Met
XM_011539849.1:c.5395C>A XP_011538151.1:p.Leu1799Met
XM_011539850.1:c.4240C>A XP_011538152.1:p.Leu1414Met
XM_006717885.4:c.5395C>A XP_006717948.1:p.Leu1799Met
XM_006717888.4:c.5392C>A XP_006717951.1:p.Leu1798Met
XM_006717889.4:c.5347C>A XP_006717952.1:p.Leu1783Met
XM_006717890.3:c.4471C>A XP_006717953.1:p.Leu1491Met
XM_011539849.3:c.5395C>A XP_011538151.1:p.Leu1799Met
XM_011539850.3:c.4240C>A XP_011538152.1:p.Leu1414Met
XM_017016310.2:c.5395C>A XP_016871799.1:p.Leu1799Met
XM_017016311.2:c.5395C>A XP_016871800.1:p.Leu1799Met
XM_017016312.2:c.4381C>A XP_016871801.1:p.Leu1461Met
NM_001288989.2:c.5305C>A NP_001275918.1:p.Leu1769Met
NM_016341.4:c.5353C>A MANE Select NP_057425.3:p.Leu1785Met