Canonical Allele Identifier: CA1928998439

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298560G= , CM000672.2:g.94298560G=	GRCh38
NC_000010.10:g.96058317G= , CM000672.1:g.96058317G=	GRCh37
NC_000010.9:g.96048307G=	NCBI36
NG_015799.1:g.309572G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4425G=	ENSP00000360426.1:p.Gln1475=
ENST00000685253.1:c.*1892G=	ENSP00000509405.1:n.*1892G=
ENST00000685889.1:n.2084G=
ENST00000686807.1:n.768G=
ENST00000686954.1:c.*633G=	ENSP00000508416.1:n.*633G=
ENST00000688810.1:c.4377G=	ENSP00000509140.1:p.Gln1459=
ENST00000689233.1:n.9557G=
ENST00000690340.1:n.3022G=
ENST00000692286.1:c.5217G=	ENSP00000509490.1:p.Gln1739=
ENST00000692396.1:c.5301G=	ENSP00000508605.1:p.Gln1767=
ENST00000371380.8:c.5349G= MANE Select	ENSP00000360431.2:p.Gln1783=
ENST00000371385.8:c.4323G=	ENSP00000360438.4:p.Gln1441=
ENST00000674738.1:c.3904G=
ENST00000674827.1:c.3465G=	ENSP00000502523.1:p.Gln1155=
ENST00000675218.1:c.4425G=	ENSP00000501910.1:p.Gln1475=
ENST00000675487.1:c.*1282G=	ENSP00000502340.1:n.*1282G=
ENST00000675718.1:c.4618G=
ENST00000260766.7:c.5349G=	ENSP00000260766.3:p.Gln1783=
ENST00000371375.1:c.4425G=	ENSP00000360426.1:p.Gln1475=
ENST00000371380.7:c.5349G=	ENSP00000360431.2:p.Gln1783=
ENST00000371385.7:c.4425G=	ENSP00000360438.3:p.Gln1475=
NM_001165979.2:c.4425G=	NP_001159451.1:p.Gln1475=
NM_001288989.1:c.5301G=	NP_001275918.1:p.Gln1767=
NM_016341.3:c.5349G=	NP_057425.3:p.Gln1783=
XM_006717885.2:c.5391G=	XP_006717948.1:p.Gln1797=
XM_006717886.2:c.5391G=	XP_006717949.1:p.Gln1797=
XM_006717888.2:c.5388G=	XP_006717951.1:p.Gln1796=
XM_006717889.2:c.5343G=	XP_006717952.1:p.Gln1781=
XM_006717890.1:c.4467G=	XP_006717953.1:p.Gln1489=
XM_011539849.1:c.5391G=	XP_011538151.1:p.Gln1797=
XM_011539850.1:c.4236G=	XP_011538152.1:p.Gln1412=
XM_006717885.4:c.5391G=	XP_006717948.1:p.Gln1797=
XM_006717888.4:c.5388G=	XP_006717951.1:p.Gln1796=
XM_006717889.4:c.5343G=	XP_006717952.1:p.Gln1781=
XM_006717890.3:c.4467G=	XP_006717953.1:p.Gln1489=
XM_011539849.3:c.5391G=	XP_011538151.1:p.Gln1797=
XM_011539850.3:c.4236G=	XP_011538152.1:p.Gln1412=
XM_017016310.2:c.5391G=	XP_016871799.1:p.Gln1797=
XM_017016311.2:c.5391G=	XP_016871800.1:p.Gln1797=
XM_017016312.2:c.4377G=	XP_016871801.1:p.Gln1459=
NM_001288989.2:c.5301G=	NP_001275918.1:p.Gln1767=
NM_016341.4:c.5349G= MANE Select	NP_057425.3:p.Gln1783=