Canonical Allele Identifier: CA1928998445
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298576C= , CM000672.2:g.94298576C= GRCh38
NC_000010.10:g.96058333C= , CM000672.1:g.96058333C= GRCh37
NC_000010.9:g.96048323C= NCBI36
NG_015799.1:g.309588C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5365C= MANE Select ENSP00000360431.2:p.Pro1789=
ENST00000371385.8:c.4339C= ENSP00000360438.4:p.Pro1447=
ENST00000674738.1:n.3920C=
ENST00000674827.1:n.3481C= ENSP00000502523.1:p.Pro1161=
ENST00000675218.1:n.4441C= ENSP00000501910.1:p.Pro1481=
ENST00000675487.1:c.*1298C= ENSP00000502340.1:p.=
ENST00000675718.1:n.4634C=
ENST00000260766.7:c.5365C= ENSP00000260766.3:p.Pro1789=
ENST00000371375.1:n.4441C= ENSP00000360426.1:p.Pro1481=
ENST00000371380.7:c.5365C= ENSP00000360431.2:p.Pro1789=
ENST00000371385.7:c.4441C= ENSP00000360438.3:p.Pro1481=
NM_001165979.2:c.4441C= NP_001159451.1:p.Pro1481=
NM_001288989.1:c.5317C= NP_001275918.1:p.Pro1773=
NM_016341.3:c.5365C= NP_057425.3:p.Pro1789=
XM_006717885.2:c.5407C= XP_006717948.1:p.Pro1803=
XM_006717886.2:c.5407C= XP_006717949.1:p.Pro1803=
XM_006717888.2:c.5404C= XP_006717951.1:p.Pro1802=
XM_006717889.2:c.5359C= XP_006717952.1:p.Pro1787=
XM_006717890.1:c.4483C= XP_006717953.1:p.Pro1495=
XM_011539849.1:c.5407C= XP_011538151.1:p.Pro1803=
XM_011539850.1:c.4252C= XP_011538152.1:p.Pro1418=
XM_006717885.4:c.5407C= XP_006717948.1:p.Pro1803=
XM_006717888.4:c.5404C= XP_006717951.1:p.Pro1802=
XM_006717889.4:c.5359C= XP_006717952.1:p.Pro1787=
XM_006717890.3:c.4483C= XP_006717953.1:p.Pro1495=
XM_011539849.3:c.5407C= XP_011538151.1:p.Pro1803=
XM_011539850.3:c.4252C= XP_011538152.1:p.Pro1418=
XM_017016310.2:c.5407C= XP_016871799.1:p.Pro1803=
XM_017016311.2:c.5407C= XP_016871800.1:p.Pro1803=
XM_017016312.2:c.4393C= XP_016871801.1:p.Pro1465=
NM_001288989.2:c.5317C= NP_001275918.1:p.Pro1773=
NM_016341.4:c.5365C= MANE Select NP_057425.3:p.Pro1789=