Canonical Allele Identifier: CA377641719
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298410G>T , CM000672.2:g.94298410G>T GRCh38
NC_000010.10:g.96058167G>T , CM000672.1:g.96058167G>T GRCh37
NC_000010.9:g.96048157G>T NCBI36
NG_015799.1:g.309422G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4275G>T ENSP00000360426.1:p.Glu1425Asp
ENST00000685253.1:c.*1742G>T ENSP00000509405.1:n.*1742G>T
ENST00000685889.1:n.1934G>T
ENST00000686807.1:n.618G>T
ENST00000686954.1:c.*483G>T ENSP00000508416.1:n.*483G>T
ENST00000688810.1:c.4227G>T ENSP00000509140.1:p.Glu1409Asp
ENST00000689233.1:n.9407G>T
ENST00000690340.1:n.2872G>T
ENST00000692286.1:c.5067G>T ENSP00000509490.1:p.Glu1689Asp
ENST00000692396.1:c.5151G>T ENSP00000508605.1:p.Glu1717Asp
ENST00000371380.8:c.5199G>T MANE Select ENSP00000360431.2:p.Glu1733Asp
ENST00000371385.8:c.4173G>T ENSP00000360438.4:p.Glu1391Asp
ENST00000674738.1:c.3754G>T
ENST00000674827.1:c.3315G>T ENSP00000502523.1:p.Glu1105Asp
ENST00000675218.1:c.4275G>T ENSP00000501910.1:p.Glu1425Asp
ENST00000675487.1:c.*1132G>T ENSP00000502340.1:n.*1132G>T
ENST00000675718.1:c.4468G>T
ENST00000676102.1:c.4044G>T ENSP00000502811.1:p.Glu1348Asp
ENST00000260766.7:c.5199G>T ENSP00000260766.3:p.Glu1733Asp
ENST00000371375.1:c.4275G>T ENSP00000360426.1:p.Glu1425Asp
ENST00000371380.7:c.5199G>T ENSP00000360431.2:p.Glu1733Asp
ENST00000371385.7:c.4275G>T ENSP00000360438.3:p.Glu1425Asp
NM_001165979.2:c.4275G>T NP_001159451.1:p.Glu1425Asp
NM_001288989.1:c.5151G>T NP_001275918.1:p.Glu1717Asp
NM_016341.3:c.5199G>T NP_057425.3:p.Glu1733Asp
XM_006717885.2:c.5241G>T XP_006717948.1:p.Glu1747Asp
XM_006717886.2:c.5241G>T XP_006717949.1:p.Glu1747Asp
XM_006717888.2:c.5238G>T XP_006717951.1:p.Glu1746Asp
XM_006717889.2:c.5193G>T XP_006717952.1:p.Glu1731Asp
XM_006717890.1:c.4317G>T XP_006717953.1:p.Glu1439Asp
XM_011539849.1:c.5241G>T XP_011538151.1:p.Glu1747Asp
XM_011539850.1:c.4086G>T XP_011538152.1:p.Glu1362Asp
XM_006717885.4:c.5241G>T XP_006717948.1:p.Glu1747Asp
XM_006717888.4:c.5238G>T XP_006717951.1:p.Glu1746Asp
XM_006717889.4:c.5193G>T XP_006717952.1:p.Glu1731Asp
XM_006717890.3:c.4317G>T XP_006717953.1:p.Glu1439Asp
XM_011539849.3:c.5241G>T XP_011538151.1:p.Glu1747Asp
XM_011539850.3:c.4086G>T XP_011538152.1:p.Glu1362Asp
XM_017016310.2:c.5241G>T XP_016871799.1:p.Glu1747Asp
XM_017016311.2:c.5241G>T XP_016871800.1:p.Glu1747Asp
XM_017016312.2:c.4227G>T XP_016871801.1:p.Glu1409Asp
NM_001288989.2:c.5151G>T NP_001275918.1:p.Glu1717Asp
NM_016341.4:c.5199G>T MANE Select NP_057425.3:p.Glu1733Asp