Canonical Allele Identifier: CA1928998426

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298524G= , CM000672.2:g.94298524G=	GRCh38
NC_000010.10:g.96058281G= , CM000672.1:g.96058281G=	GRCh37
NC_000010.9:g.96048271G=	NCBI36
NG_015799.1:g.309536G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4389G=	ENSP00000360426.1:p.Arg1463=
ENST00000685253.1:c.*1856G=	ENSP00000509405.1:n.*1856G=
ENST00000685889.1:n.2048G=
ENST00000686807.1:n.732G=
ENST00000686954.1:c.*597G=	ENSP00000508416.1:n.*597G=
ENST00000688810.1:c.4341G=	ENSP00000509140.1:p.Arg1447=
ENST00000689233.1:n.9521G=
ENST00000690340.1:n.2986G=
ENST00000692286.1:c.5181G=	ENSP00000509490.1:p.Arg1727=
ENST00000692396.1:c.5265G=	ENSP00000508605.1:p.Arg1755=
ENST00000371380.8:c.5313G= MANE Select	ENSP00000360431.2:p.Arg1771=
ENST00000371385.8:c.4287G=	ENSP00000360438.4:p.Arg1429=
ENST00000674738.1:c.3868G=
ENST00000674827.1:c.3429G=	ENSP00000502523.1:p.Arg1143=
ENST00000675218.1:c.4389G=	ENSP00000501910.1:p.Arg1463=
ENST00000675487.1:c.*1246G=	ENSP00000502340.1:n.*1246G=
ENST00000675718.1:c.4582G=
ENST00000260766.7:c.5313G=	ENSP00000260766.3:p.Arg1771=
ENST00000371375.1:c.4389G=	ENSP00000360426.1:p.Arg1463=
ENST00000371380.7:c.5313G=	ENSP00000360431.2:p.Arg1771=
ENST00000371385.7:c.4389G=	ENSP00000360438.3:p.Arg1463=
NM_001165979.2:c.4389G=	NP_001159451.1:p.Arg1463=
NM_001288989.1:c.5265G=	NP_001275918.1:p.Arg1755=
NM_016341.3:c.5313G=	NP_057425.3:p.Arg1771=
XM_006717885.2:c.5355G=	XP_006717948.1:p.Arg1785=
XM_006717886.2:c.5355G=	XP_006717949.1:p.Arg1785=
XM_006717888.2:c.5352G=	XP_006717951.1:p.Arg1784=
XM_006717889.2:c.5307G=	XP_006717952.1:p.Arg1769=
XM_006717890.1:c.4431G=	XP_006717953.1:p.Arg1477=
XM_011539849.1:c.5355G=	XP_011538151.1:p.Arg1785=
XM_011539850.1:c.4200G=	XP_011538152.1:p.Arg1400=
XM_006717885.4:c.5355G=	XP_006717948.1:p.Arg1785=
XM_006717888.4:c.5352G=	XP_006717951.1:p.Arg1784=
XM_006717889.4:c.5307G=	XP_006717952.1:p.Arg1769=
XM_006717890.3:c.4431G=	XP_006717953.1:p.Arg1477=
XM_011539849.3:c.5355G=	XP_011538151.1:p.Arg1785=
XM_011539850.3:c.4200G=	XP_011538152.1:p.Arg1400=
XM_017016310.2:c.5355G=	XP_016871799.1:p.Arg1785=
XM_017016311.2:c.5355G=	XP_016871800.1:p.Arg1785=
XM_017016312.2:c.4341G=	XP_016871801.1:p.Arg1447=
NM_001288989.2:c.5265G=	NP_001275918.1:p.Arg1755=
NM_016341.4:c.5313G= MANE Select	NP_057425.3:p.Arg1771=