Canonical Allele Identifier: CA2842464917

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94322027dup , CM000672.2:g.94322027dup GRCh38
NC_000010.10:g.96081784dup , CM000672.1:g.96081784dup GRCh37
NC_000010.9:g.96071774dup NCBI36
NG_015799.1:g.333039dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371375.2:c.5545dup (PLCE1) ENSP00000360426.1:p.Arg1849ProfsTer?
ENST00000685132.1:n.3868dup (PLCE1)
ENST00000685253.1:c.*3012dup (PLCE1) ENSP00000509405.1:n.*3012dup
ENST00000685889.1:n.3204dup (PLCE1)
ENST00000686807.1:n.1888dup (PLCE1)
ENST00000686954.1:c.*1753dup (PLCE1) ENSP00000508416.1:n.*1753dup
ENST00000688810.1:c.5497dup (PLCE1) ENSP00000509140.1:p.Arg1833ProfsTer?
ENST00000689233.1:n.10677dup (PLCE1)
ENST00000690340.1:n.4142dup (PLCE1)
ENST00000692286.1:c.6337dup (PLCE1) ENSP00000509490.1:p.Arg2113ProfsTer?
ENST00000692396.1:c.6421dup (PLCE1) ENSP00000508605.1:p.Arg2141ProfsTer?
ENST00000371380.8:c.6469dup (PLCE1) MANE Select ENSP00000360431.2:p.Arg2157ProfsTer?
ENST00000371385.8:c.5443dup (PLCE1) ENSP00000360438.4:p.Arg1815ProfsTer?
ENST00000674738.1:c.5024dup (PLCE1)
ENST00000675218.1:c.5545dup (PLCE1) ENSP00000501910.1:p.Arg1849ProfsTer?
ENST00000675487.1:c.*2402dup (PLCE1) ENSP00000502340.1:n.*2402dup
ENST00000675718.1:c.5738dup (PLCE1)
ENST00000260766.7:c.6469dup (PLCE1) ENSP00000260766.3:p.Arg2157ProfsTer?
ENST00000371375.1:c.5545dup (PLCE1) ENSP00000360426.1:p.Arg1849ProfsTer?
ENST00000371380.7:c.6469dup (PLCE1) ENSP00000360431.2:p.Arg2157ProfsTer?
ENST00000371385.7:c.5545dup (PLCE1) ENSP00000360438.3:p.Arg1849ProfsTer?
NM_001165979.2:c.5545dup (PLCE1) NP_001159451.1:p.Arg1849ProfsTer?
NM_001288989.1:c.6421dup (PLCE1) NP_001275918.1:p.Arg2141ProfsTer?
NM_016341.3:c.6469dup (PLCE1) NP_057425.3:p.Arg2157ProfsTer?
XM_006717885.2:c.6511dup (PLCE1) XP_006717948.1:p.Arg2171ProfsTer?
XM_006717886.2:c.6511dup (PLCE1) XP_006717949.1:p.Arg2171ProfsTer?
XM_006717888.2:c.6508dup (PLCE1) XP_006717951.1:p.Arg2170ProfsTer?
XM_006717889.2:c.6463dup (PLCE1) XP_006717952.1:p.Arg2155ProfsTer?
XM_006717890.1:c.5587dup (PLCE1) XP_006717953.1:p.Arg1863ProfsTer?
XM_011539849.1:c.6511dup (PLCE1) XP_011538151.1:p.Arg2171ProfsTer?
XM_011539850.1:c.5356dup (PLCE1) XP_011538152.1:p.Arg1786ProfsTer?
XR_945799.1:n.3311-6560dup (NOC3L)
XM_006717885.4:c.6511dup (PLCE1) XP_006717948.1:p.Arg2171ProfsTer?
XM_006717888.4:c.6508dup (PLCE1) XP_006717951.1:p.Arg2170ProfsTer?
XM_006717889.4:c.6463dup (PLCE1) XP_006717952.1:p.Arg2155ProfsTer?
XM_006717890.3:c.5587dup (PLCE1) XP_006717953.1:p.Arg1863ProfsTer?
XM_011539849.3:c.6511dup (PLCE1) XP_011538151.1:p.Arg2171ProfsTer?
XM_011539850.3:c.5356dup (PLCE1) XP_011538152.1:p.Arg1786ProfsTer?
XM_017016310.2:c.6511dup (PLCE1) XP_016871799.1:p.Arg2171ProfsTer?
XM_017016311.2:c.6511dup (PLCE1) XP_016871800.1:p.Arg2171ProfsTer?
XM_017016312.2:c.5497dup (PLCE1) XP_016871801.1:p.Arg1833ProfsTer?
XR_002957007.1:n.3312-6560dup (NOC3L)
NM_001288989.2:c.6421dup (PLCE1) NP_001275918.1:p.Arg2141ProfsTer?
NM_016341.4:c.6469dup (PLCE1) MANE Select NP_057425.3:p.Arg2157ProfsTer?