Canonical Allele Identifier: CA1928998376
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298405T= , CM000672.2:g.94298405T= GRCh38
NC_000010.10:g.96058162T= , CM000672.1:g.96058162T= GRCh37
NC_000010.9:g.96048152T= NCBI36
NG_015799.1:g.309417T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4270T= ENSP00000360426.1:p.Trp1424=
ENST00000685253.1:c.*1737T= ENSP00000509405.1:n.*1737T=
ENST00000685889.1:n.1929T=
ENST00000686807.1:n.613T=
ENST00000686954.1:c.*478T= ENSP00000508416.1:n.*478T=
ENST00000688810.1:c.4222T= ENSP00000509140.1:p.Trp1408=
ENST00000689233.1:n.9402T=
ENST00000690340.1:n.2867T=
ENST00000692286.1:c.5062T= ENSP00000509490.1:p.Trp1688=
ENST00000692396.1:c.5146T= ENSP00000508605.1:p.Trp1716=
ENST00000371380.8:c.5194T= MANE Select ENSP00000360431.2:p.Trp1732=
ENST00000371385.8:c.4168T= ENSP00000360438.4:p.Trp1390=
ENST00000674738.1:c.3749T=
ENST00000674827.1:c.3310T= ENSP00000502523.1:p.Trp1104=
ENST00000675218.1:c.4270T= ENSP00000501910.1:p.Trp1424=
ENST00000675487.1:c.*1127T= ENSP00000502340.1:n.*1127T=
ENST00000675718.1:c.4463T=
ENST00000676102.1:c.4039T= ENSP00000502811.1:p.Trp1347=
ENST00000260766.7:c.5194T= ENSP00000260766.3:p.Trp1732=
ENST00000371375.1:c.4270T= ENSP00000360426.1:p.Trp1424=
ENST00000371380.7:c.5194T= ENSP00000360431.2:p.Trp1732=
ENST00000371385.7:c.4270T= ENSP00000360438.3:p.Trp1424=
NM_001165979.2:c.4270T= NP_001159451.1:p.Trp1424=
NM_001288989.1:c.5146T= NP_001275918.1:p.Trp1716=
NM_016341.3:c.5194T= NP_057425.3:p.Trp1732=
XM_006717885.2:c.5236T= XP_006717948.1:p.Trp1746=
XM_006717886.2:c.5236T= XP_006717949.1:p.Trp1746=
XM_006717888.2:c.5233T= XP_006717951.1:p.Trp1745=
XM_006717889.2:c.5188T= XP_006717952.1:p.Trp1730=
XM_006717890.1:c.4312T= XP_006717953.1:p.Trp1438=
XM_011539849.1:c.5236T= XP_011538151.1:p.Trp1746=
XM_011539850.1:c.4081T= XP_011538152.1:p.Trp1361=
XM_006717885.4:c.5236T= XP_006717948.1:p.Trp1746=
XM_006717888.4:c.5233T= XP_006717951.1:p.Trp1745=
XM_006717889.4:c.5188T= XP_006717952.1:p.Trp1730=
XM_006717890.3:c.4312T= XP_006717953.1:p.Trp1438=
XM_011539849.3:c.5236T= XP_011538151.1:p.Trp1746=
XM_011539850.3:c.4081T= XP_011538152.1:p.Trp1361=
XM_017016310.2:c.5236T= XP_016871799.1:p.Trp1746=
XM_017016311.2:c.5236T= XP_016871800.1:p.Trp1746=
XM_017016312.2:c.4222T= XP_016871801.1:p.Trp1408=
NM_001288989.2:c.5146T= NP_001275918.1:p.Trp1716=
NM_016341.4:c.5194T= MANE Select NP_057425.3:p.Trp1732=