Canonical Allele Identifier: CA1928996187

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293543G= , CM000672.2:g.94293543G=	GRCh38
NC_000010.10:g.96053300G= , CM000672.1:g.96053300G=	GRCh37
NC_000010.9:g.96043290G=	NCBI36
NG_015799.1:g.304555G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4147G=	ENSP00000360426.1:p.Gly1383=
ENST00000685253.1:c.*1614G=	ENSP00000509405.1:n.*1614G=
ENST00000685889.1:n.1806G=
ENST00000686807.1:n.490G=
ENST00000686954.1:c.*355G=	ENSP00000508416.1:n.*355G=
ENST00000688810.1:c.4099G=	ENSP00000509140.1:p.Gly1367=
ENST00000689233.1:n.9279G=
ENST00000690340.1:n.2744G=
ENST00000692286.1:c.5036-4836G=	ENSP00000509490.1:n.5036-4836G=
ENST00000692396.1:c.5023G=	ENSP00000508605.1:p.Gly1675=
ENST00000371380.8:c.5071G= MANE Select	ENSP00000360431.2:p.Gly1691=
ENST00000371385.8:c.4045G=	ENSP00000360438.4:p.Gly1349=
ENST00000674738.1:c.3626G=
ENST00000674827.1:c.3187G=	ENSP00000502523.1:p.Gly1063=
ENST00000675218.1:c.4147G=	ENSP00000501910.1:p.Gly1383=
ENST00000675487.1:c.*1004G=	ENSP00000502340.1:n.*1004G=
ENST00000675718.1:c.4340G=
ENST00000676102.1:c.3916G=	ENSP00000502811.1:p.Gly1306=
ENST00000260766.7:c.5071G=	ENSP00000260766.3:p.Gly1691=
ENST00000371375.1:c.4147G=	ENSP00000360426.1:p.Gly1383=
ENST00000371380.7:c.5071G=	ENSP00000360431.2:p.Gly1691=
ENST00000371385.7:c.4147G=	ENSP00000360438.3:p.Gly1383=
NM_001165979.2:c.4147G=	NP_001159451.1:p.Gly1383=
NM_001288989.1:c.5023G=	NP_001275918.1:p.Gly1675=
NM_016341.3:c.5071G=	NP_057425.3:p.Gly1691=
XM_006717885.2:c.5113G=	XP_006717948.1:p.Gly1705=
XM_006717886.2:c.5113G=	XP_006717949.1:p.Gly1705=
XM_006717888.2:c.5110G=	XP_006717951.1:p.Gly1704=
XM_006717889.2:c.5065G=	XP_006717952.1:p.Gly1689=
XM_006717890.1:c.4189G=	XP_006717953.1:p.Gly1397=
XM_011539849.1:c.5113G=	XP_011538151.1:p.Gly1705=
XM_011539850.1:c.3958G=	XP_011538152.1:p.Gly1320=
XM_006717885.4:c.5113G=	XP_006717948.1:p.Gly1705=
XM_006717888.4:c.5110G=	XP_006717951.1:p.Gly1704=
XM_006717889.4:c.5065G=	XP_006717952.1:p.Gly1689=
XM_006717890.3:c.4189G=	XP_006717953.1:p.Gly1397=
XM_011539849.3:c.5113G=	XP_011538151.1:p.Gly1705=
XM_011539850.3:c.3958G=	XP_011538152.1:p.Gly1320=
XM_017016310.2:c.5113G=	XP_016871799.1:p.Gly1705=
XM_017016311.2:c.5113G=	XP_016871800.1:p.Gly1705=
XM_017016312.2:c.4099G=	XP_016871801.1:p.Gly1367=
NM_001288989.2:c.5023G=	NP_001275918.1:p.Gly1675=
NM_016341.4:c.5071G= MANE Select	NP_057425.3:p.Gly1691=