Canonical Allele Identifier: CA1928998443
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298572T= , CM000672.2:g.94298572T= GRCh38
NC_000010.10:g.96058329T= , CM000672.1:g.96058329T= GRCh37
NC_000010.9:g.96048319T= NCBI36
NG_015799.1:g.309584T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5361T= MANE Select ENSP00000360431.2:p.Thr1787=
ENST00000371385.8:c.4335T= ENSP00000360438.4:p.Thr1445=
ENST00000674738.1:n.3916T=
ENST00000674827.1:n.3477T= ENSP00000502523.1:p.Thr1159=
ENST00000675218.1:n.4437T= ENSP00000501910.1:p.Thr1479=
ENST00000675487.1:c.*1294T= ENSP00000502340.1:p.=
ENST00000675718.1:n.4630T=
ENST00000260766.7:c.5361T= ENSP00000260766.3:p.Thr1787=
ENST00000371375.1:n.4437T= ENSP00000360426.1:p.Thr1479=
ENST00000371380.7:c.5361T= ENSP00000360431.2:p.Thr1787=
ENST00000371385.7:c.4437T= ENSP00000360438.3:p.Thr1479=
NM_001165979.2:c.4437T= NP_001159451.1:p.Thr1479=
NM_001288989.1:c.5313T= NP_001275918.1:p.Thr1771=
NM_016341.3:c.5361T= NP_057425.3:p.Thr1787=
XM_006717885.2:c.5403T= XP_006717948.1:p.Thr1801=
XM_006717886.2:c.5403T= XP_006717949.1:p.Thr1801=
XM_006717888.2:c.5400T= XP_006717951.1:p.Thr1800=
XM_006717889.2:c.5355T= XP_006717952.1:p.Thr1785=
XM_006717890.1:c.4479T= XP_006717953.1:p.Thr1493=
XM_011539849.1:c.5403T= XP_011538151.1:p.Thr1801=
XM_011539850.1:c.4248T= XP_011538152.1:p.Thr1416=
XM_006717885.4:c.5403T= XP_006717948.1:p.Thr1801=
XM_006717888.4:c.5400T= XP_006717951.1:p.Thr1800=
XM_006717889.4:c.5355T= XP_006717952.1:p.Thr1785=
XM_006717890.3:c.4479T= XP_006717953.1:p.Thr1493=
XM_011539849.3:c.5403T= XP_011538151.1:p.Thr1801=
XM_011539850.3:c.4248T= XP_011538152.1:p.Thr1416=
XM_017016310.2:c.5403T= XP_016871799.1:p.Thr1801=
XM_017016311.2:c.5403T= XP_016871800.1:p.Thr1801=
XM_017016312.2:c.4389T= XP_016871801.1:p.Thr1463=
NM_001288989.2:c.5313T= NP_001275918.1:p.Thr1771=
NM_016341.4:c.5361T= MANE Select NP_057425.3:p.Thr1787=