Canonical Allele Identifier: CA1928998379

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298411G= , CM000672.2:g.94298411G=	GRCh38
NC_000010.10:g.96058168G= , CM000672.1:g.96058168G=	GRCh37
NC_000010.9:g.96048158G=	NCBI36
NG_015799.1:g.309423G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4276G=	ENSP00000360426.1:p.Glu1426=
ENST00000685253.1:c.*1743G=	ENSP00000509405.1:n.*1743G=
ENST00000685889.1:n.1935G=
ENST00000686807.1:n.619G=
ENST00000686954.1:c.*484G=	ENSP00000508416.1:n.*484G=
ENST00000688810.1:c.4228G=	ENSP00000509140.1:p.Glu1410=
ENST00000689233.1:n.9408G=
ENST00000690340.1:n.2873G=
ENST00000692286.1:c.5068G=	ENSP00000509490.1:p.Glu1690=
ENST00000692396.1:c.5152G=	ENSP00000508605.1:p.Glu1718=
ENST00000371380.8:c.5200G= MANE Select	ENSP00000360431.2:p.Glu1734=
ENST00000371385.8:c.4174G=	ENSP00000360438.4:p.Glu1392=
ENST00000674738.1:c.3755G=
ENST00000674827.1:c.3316G=	ENSP00000502523.1:p.Glu1106=
ENST00000675218.1:c.4276G=	ENSP00000501910.1:p.Glu1426=
ENST00000675487.1:c.*1133G=	ENSP00000502340.1:n.*1133G=
ENST00000675718.1:c.4469G=
ENST00000676102.1:c.4045G=	ENSP00000502811.1:p.Glu1349=
ENST00000260766.7:c.5200G=	ENSP00000260766.3:p.Glu1734=
ENST00000371375.1:c.4276G=	ENSP00000360426.1:p.Glu1426=
ENST00000371380.7:c.5200G=	ENSP00000360431.2:p.Glu1734=
ENST00000371385.7:c.4276G=	ENSP00000360438.3:p.Glu1426=
NM_001165979.2:c.4276G=	NP_001159451.1:p.Glu1426=
NM_001288989.1:c.5152G=	NP_001275918.1:p.Glu1718=
NM_016341.3:c.5200G=	NP_057425.3:p.Glu1734=
XM_006717885.2:c.5242G=	XP_006717948.1:p.Glu1748=
XM_006717886.2:c.5242G=	XP_006717949.1:p.Glu1748=
XM_006717888.2:c.5239G=	XP_006717951.1:p.Glu1747=
XM_006717889.2:c.5194G=	XP_006717952.1:p.Glu1732=
XM_006717890.1:c.4318G=	XP_006717953.1:p.Glu1440=
XM_011539849.1:c.5242G=	XP_011538151.1:p.Glu1748=
XM_011539850.1:c.4087G=	XP_011538152.1:p.Glu1363=
XM_006717885.4:c.5242G=	XP_006717948.1:p.Glu1748=
XM_006717888.4:c.5239G=	XP_006717951.1:p.Glu1747=
XM_006717889.4:c.5194G=	XP_006717952.1:p.Glu1732=
XM_006717890.3:c.4318G=	XP_006717953.1:p.Glu1440=
XM_011539849.3:c.5242G=	XP_011538151.1:p.Glu1748=
XM_011539850.3:c.4087G=	XP_011538152.1:p.Glu1363=
XM_017016310.2:c.5242G=	XP_016871799.1:p.Glu1748=
XM_017016311.2:c.5242G=	XP_016871800.1:p.Glu1748=
XM_017016312.2:c.4228G=	XP_016871801.1:p.Glu1410=
NM_001288989.2:c.5152G=	NP_001275918.1:p.Glu1718=
NM_016341.4:c.5200G= MANE Select	NP_057425.3:p.Glu1734=