Canonical Allele Identifier: CA1928998420

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298511G= , CM000672.2:g.94298511G=	GRCh38
NC_000010.10:g.96058268G= , CM000672.1:g.96058268G=	GRCh37
NC_000010.9:g.96048258G=	NCBI36
NG_015799.1:g.309523G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4376G=	ENSP00000360426.1:p.Arg1459=
ENST00000685253.1:c.*1843G=	ENSP00000509405.1:n.*1843G=
ENST00000685889.1:n.2035G=
ENST00000686807.1:n.719G=
ENST00000686954.1:c.*584G=	ENSP00000508416.1:n.*584G=
ENST00000688810.1:c.4328G=	ENSP00000509140.1:p.Arg1443=
ENST00000689233.1:n.9508G=
ENST00000690340.1:n.2973G=
ENST00000692286.1:c.5168G=	ENSP00000509490.1:p.Arg1723=
ENST00000692396.1:c.5252G=	ENSP00000508605.1:p.Arg1751=
ENST00000371380.8:c.5300G= MANE Select	ENSP00000360431.2:p.Arg1767=
ENST00000371385.8:c.4274G=	ENSP00000360438.4:p.Arg1425=
ENST00000674738.1:c.3855G=
ENST00000674827.1:c.3416G=	ENSP00000502523.1:p.Arg1139=
ENST00000675218.1:c.4376G=	ENSP00000501910.1:p.Arg1459=
ENST00000675487.1:c.*1233G=	ENSP00000502340.1:n.*1233G=
ENST00000675718.1:c.4569G=
ENST00000260766.7:c.5300G=	ENSP00000260766.3:p.Arg1767=
ENST00000371375.1:c.4376G=	ENSP00000360426.1:p.Arg1459=
ENST00000371380.7:c.5300G=	ENSP00000360431.2:p.Arg1767=
ENST00000371385.7:c.4376G=	ENSP00000360438.3:p.Arg1459=
NM_001165979.2:c.4376G=	NP_001159451.1:p.Arg1459=
NM_001288989.1:c.5252G=	NP_001275918.1:p.Arg1751=
NM_016341.3:c.5300G=	NP_057425.3:p.Arg1767=
XM_006717885.2:c.5342G=	XP_006717948.1:p.Arg1781=
XM_006717886.2:c.5342G=	XP_006717949.1:p.Arg1781=
XM_006717888.2:c.5339G=	XP_006717951.1:p.Arg1780=
XM_006717889.2:c.5294G=	XP_006717952.1:p.Arg1765=
XM_006717890.1:c.4418G=	XP_006717953.1:p.Arg1473=
XM_011539849.1:c.5342G=	XP_011538151.1:p.Arg1781=
XM_011539850.1:c.4187G=	XP_011538152.1:p.Arg1396=
XM_006717885.4:c.5342G=	XP_006717948.1:p.Arg1781=
XM_006717888.4:c.5339G=	XP_006717951.1:p.Arg1780=
XM_006717889.4:c.5294G=	XP_006717952.1:p.Arg1765=
XM_006717890.3:c.4418G=	XP_006717953.1:p.Arg1473=
XM_011539849.3:c.5342G=	XP_011538151.1:p.Arg1781=
XM_011539850.3:c.4187G=	XP_011538152.1:p.Arg1396=
XM_017016310.2:c.5342G=	XP_016871799.1:p.Arg1781=
XM_017016311.2:c.5342G=	XP_016871800.1:p.Arg1781=
XM_017016312.2:c.4328G=	XP_016871801.1:p.Arg1443=
NM_001288989.2:c.5252G=	NP_001275918.1:p.Arg1751=
NM_016341.4:c.5300G= MANE Select	NP_057425.3:p.Arg1767=