Canonical Allele Identifier: CA1928996186

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293541G= , CM000672.2:g.94293541G=	GRCh38
NC_000010.10:g.96053298G= , CM000672.1:g.96053298G=	GRCh37
NC_000010.9:g.96043288G=	NCBI36
NG_015799.1:g.304553G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4145G=	ENSP00000360426.1:p.Arg1382=
ENST00000685253.1:c.*1612G=	ENSP00000509405.1:n.*1612G=
ENST00000685889.1:n.1804G=
ENST00000686807.1:n.488G=
ENST00000686954.1:c.*353G=	ENSP00000508416.1:n.*353G=
ENST00000688810.1:c.4097G=	ENSP00000509140.1:p.Arg1366=
ENST00000689233.1:n.9277G=
ENST00000690340.1:n.2742G=
ENST00000692286.1:c.5036-4838G=	ENSP00000509490.1:n.5036-4838G=
ENST00000692396.1:c.5021G=	ENSP00000508605.1:p.Arg1674=
ENST00000371380.8:c.5069G= MANE Select	ENSP00000360431.2:p.Arg1690=
ENST00000371385.8:c.4043G=	ENSP00000360438.4:p.Arg1348=
ENST00000674738.1:c.3624G=
ENST00000674827.1:c.3185G=	ENSP00000502523.1:p.Arg1062=
ENST00000675218.1:c.4145G=	ENSP00000501910.1:p.Arg1382=
ENST00000675487.1:c.*1002G=	ENSP00000502340.1:n.*1002G=
ENST00000675718.1:c.4338G=
ENST00000676102.1:c.3914G=	ENSP00000502811.1:p.Arg1305=
ENST00000260766.7:c.5069G=	ENSP00000260766.3:p.Arg1690=
ENST00000371375.1:c.4145G=	ENSP00000360426.1:p.Arg1382=
ENST00000371380.7:c.5069G=	ENSP00000360431.2:p.Arg1690=
ENST00000371385.7:c.4145G=	ENSP00000360438.3:p.Arg1382=
NM_001165979.2:c.4145G=	NP_001159451.1:p.Arg1382=
NM_001288989.1:c.5021G=	NP_001275918.1:p.Arg1674=
NM_016341.3:c.5069G=	NP_057425.3:p.Arg1690=
XM_006717885.2:c.5111G=	XP_006717948.1:p.Arg1704=
XM_006717886.2:c.5111G=	XP_006717949.1:p.Arg1704=
XM_006717888.2:c.5108G=	XP_006717951.1:p.Arg1703=
XM_006717889.2:c.5063G=	XP_006717952.1:p.Arg1688=
XM_006717890.1:c.4187G=	XP_006717953.1:p.Arg1396=
XM_011539849.1:c.5111G=	XP_011538151.1:p.Arg1704=
XM_011539850.1:c.3956G=	XP_011538152.1:p.Arg1319=
XM_006717885.4:c.5111G=	XP_006717948.1:p.Arg1704=
XM_006717888.4:c.5108G=	XP_006717951.1:p.Arg1703=
XM_006717889.4:c.5063G=	XP_006717952.1:p.Arg1688=
XM_006717890.3:c.4187G=	XP_006717953.1:p.Arg1396=
XM_011539849.3:c.5111G=	XP_011538151.1:p.Arg1704=
XM_011539850.3:c.3956G=	XP_011538152.1:p.Arg1319=
XM_017016310.2:c.5111G=	XP_016871799.1:p.Arg1704=
XM_017016311.2:c.5111G=	XP_016871800.1:p.Arg1704=
XM_017016312.2:c.4097G=	XP_016871801.1:p.Arg1366=
NM_001288989.2:c.5021G=	NP_001275918.1:p.Arg1674=
NM_016341.4:c.5069G= MANE Select	NP_057425.3:p.Arg1690=