Canonical Allele Identifier: CA1928998447

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298588C= , CM000672.2:g.94298588C=	GRCh38
NC_000010.10:g.96058345C= , CM000672.1:g.96058345C=	GRCh37
NC_000010.9:g.96048335C=	NCBI36
NG_015799.1:g.309600C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4453C=	ENSP00000360426.1:p.Arg1485=
ENST00000685253.1:c.*1920C=	ENSP00000509405.1:n.*1920C=
ENST00000685889.1:n.2112C=
ENST00000686807.1:n.796C=
ENST00000686954.1:c.*661C=	ENSP00000508416.1:n.*661C=
ENST00000688810.1:c.4405C=	ENSP00000509140.1:p.Arg1469=
ENST00000689233.1:n.9585C=
ENST00000690340.1:n.3050C=
ENST00000692286.1:c.5245C=	ENSP00000509490.1:p.Arg1749=
ENST00000692396.1:c.5329C=	ENSP00000508605.1:p.Arg1777=
ENST00000371380.8:c.5377C= MANE Select	ENSP00000360431.2:p.Arg1793=
ENST00000371385.8:c.4351C=	ENSP00000360438.4:p.Arg1451=
ENST00000674738.1:c.3932C=
ENST00000674827.1:c.3493C=	ENSP00000502523.1:p.Arg1165=
ENST00000675218.1:c.4453C=	ENSP00000501910.1:p.Arg1485=
ENST00000675487.1:c.*1310C=	ENSP00000502340.1:n.*1310C=
ENST00000675718.1:c.4646C=
ENST00000260766.7:c.5377C=	ENSP00000260766.3:p.Arg1793=
ENST00000371375.1:c.4453C=	ENSP00000360426.1:p.Arg1485=
ENST00000371380.7:c.5377C=	ENSP00000360431.2:p.Arg1793=
ENST00000371385.7:c.4453C=	ENSP00000360438.3:p.Arg1485=
NM_001165979.2:c.4453C=	NP_001159451.1:p.Arg1485=
NM_001288989.1:c.5329C=	NP_001275918.1:p.Arg1777=
NM_016341.3:c.5377C=	NP_057425.3:p.Arg1793=
XM_006717885.2:c.5419C=	XP_006717948.1:p.Arg1807=
XM_006717886.2:c.5419C=	XP_006717949.1:p.Arg1807=
XM_006717888.2:c.5416C=	XP_006717951.1:p.Arg1806=
XM_006717889.2:c.5371C=	XP_006717952.1:p.Arg1791=
XM_006717890.1:c.4495C=	XP_006717953.1:p.Arg1499=
XM_011539849.1:c.5419C=	XP_011538151.1:p.Arg1807=
XM_011539850.1:c.4264C=	XP_011538152.1:p.Arg1422=
XM_006717885.4:c.5419C=	XP_006717948.1:p.Arg1807=
XM_006717888.4:c.5416C=	XP_006717951.1:p.Arg1806=
XM_006717889.4:c.5371C=	XP_006717952.1:p.Arg1791=
XM_006717890.3:c.4495C=	XP_006717953.1:p.Arg1499=
XM_011539849.3:c.5419C=	XP_011538151.1:p.Arg1807=
XM_011539850.3:c.4264C=	XP_011538152.1:p.Arg1422=
XM_017016310.2:c.5419C=	XP_016871799.1:p.Arg1807=
XM_017016311.2:c.5419C=	XP_016871800.1:p.Arg1807=
XM_017016312.2:c.4405C=	XP_016871801.1:p.Arg1469=
NM_001288989.2:c.5329C=	NP_001275918.1:p.Arg1777=
NM_016341.4:c.5377C= MANE Select	NP_057425.3:p.Arg1793=