Canonical Allele Identifier: CA1928996185

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293540A= , CM000672.2:g.94293540A=	GRCh38
NC_000010.10:g.96053297A= , CM000672.1:g.96053297A=	GRCh37
NC_000010.9:g.96043287A=	NCBI36
NG_015799.1:g.304552A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4144A=	ENSP00000360426.1:p.Arg1382=
ENST00000685253.1:c.*1611A=	ENSP00000509405.1:n.*1611A=
ENST00000685889.1:n.1803A=
ENST00000686807.1:n.487A=
ENST00000686954.1:c.*352A=	ENSP00000508416.1:n.*352A=
ENST00000688810.1:c.4096A=	ENSP00000509140.1:p.Arg1366=
ENST00000689233.1:n.9276A=
ENST00000690340.1:n.2741A=
ENST00000692286.1:c.5036-4839A=	ENSP00000509490.1:n.5036-4839A=
ENST00000692396.1:c.5020A=	ENSP00000508605.1:p.Arg1674=
ENST00000371380.8:c.5068A= MANE Select	ENSP00000360431.2:p.Arg1690=
ENST00000371385.8:c.4042A=	ENSP00000360438.4:p.Arg1348=
ENST00000674738.1:c.3623A=
ENST00000674827.1:c.3184A=	ENSP00000502523.1:p.Arg1062=
ENST00000675218.1:c.4144A=	ENSP00000501910.1:p.Arg1382=
ENST00000675487.1:c.*1001A=	ENSP00000502340.1:n.*1001A=
ENST00000675718.1:c.4337A=
ENST00000676102.1:c.3913A=	ENSP00000502811.1:p.Arg1305=
ENST00000260766.7:c.5068A=	ENSP00000260766.3:p.Arg1690=
ENST00000371375.1:c.4144A=	ENSP00000360426.1:p.Arg1382=
ENST00000371380.7:c.5068A=	ENSP00000360431.2:p.Arg1690=
ENST00000371385.7:c.4144A=	ENSP00000360438.3:p.Arg1382=
NM_001165979.2:c.4144A=	NP_001159451.1:p.Arg1382=
NM_001288989.1:c.5020A=	NP_001275918.1:p.Arg1674=
NM_016341.3:c.5068A=	NP_057425.3:p.Arg1690=
XM_006717885.2:c.5110A=	XP_006717948.1:p.Arg1704=
XM_006717886.2:c.5110A=	XP_006717949.1:p.Arg1704=
XM_006717888.2:c.5107A=	XP_006717951.1:p.Arg1703=
XM_006717889.2:c.5062A=	XP_006717952.1:p.Arg1688=
XM_006717890.1:c.4186A=	XP_006717953.1:p.Arg1396=
XM_011539849.1:c.5110A=	XP_011538151.1:p.Arg1704=
XM_011539850.1:c.3955A=	XP_011538152.1:p.Arg1319=
XM_006717885.4:c.5110A=	XP_006717948.1:p.Arg1704=
XM_006717888.4:c.5107A=	XP_006717951.1:p.Arg1703=
XM_006717889.4:c.5062A=	XP_006717952.1:p.Arg1688=
XM_006717890.3:c.4186A=	XP_006717953.1:p.Arg1396=
XM_011539849.3:c.5110A=	XP_011538151.1:p.Arg1704=
XM_011539850.3:c.3955A=	XP_011538152.1:p.Arg1319=
XM_017016310.2:c.5110A=	XP_016871799.1:p.Arg1704=
XM_017016311.2:c.5110A=	XP_016871800.1:p.Arg1704=
XM_017016312.2:c.4096A=	XP_016871801.1:p.Arg1366=
NM_001288989.2:c.5020A=	NP_001275918.1:p.Arg1674=
NM_016341.4:c.5068A= MANE Select	NP_057425.3:p.Arg1690=