Canonical Allele Identifier: CA1928990318

Gene: PLCE1 PLCE1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94283840C= , CM000672.2:g.94283840C=	GRCh38
NC_000010.10:g.96043597C= , CM000672.1:g.96043597C=	GRCh37
NC_000010.9:g.96033587C=	NCBI36
NG_015799.1:g.294852C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016341.4:c.4846C= (PLCE1) MANE Select	NP_057425.3:p.Gln1616=
ENST00000371380.8:c.4846C= (PLCE1) MANE Select	ENSP00000360431.2:p.Gln1616=
NM_001165979.2:c.3922C= (PLCE1)	NP_001159451.1:p.Gln1308=
NM_001288989.1:c.4798C= (PLCE1)	NP_001275918.1:p.Gln1600=
NM_001288989.2:c.4798C= (PLCE1)	NP_001275918.1:p.Gln1600=
NM_016341.3:c.4846C= (PLCE1)	NP_057425.3:p.Gln1616=
NR_033969.1:n.231-354G= (PLCE1-AS1)
ENST00000260766.7:c.4846C= (PLCE1)	ENSP00000260766.3:p.Gln1616=
ENST00000371375.1:c.3922C= (PLCE1)	ENSP00000360426.1:p.Gln1308=
ENST00000371375.2:c.3922C= (PLCE1)	ENSP00000360426.1:p.Gln1308=
ENST00000371380.7:c.4846C= (PLCE1)	ENSP00000360431.2:p.Gln1616=
ENST00000371385.7:c.3922C= (PLCE1)	ENSP00000360438.3:p.Gln1308=
ENST00000371385.8:c.3820C= (PLCE1)	ENSP00000360438.4:p.Gln1274=
ENST00000674738.1:c.3401C= (PLCE1)
ENST00000674827.1:c.2962C= (PLCE1)	ENSP00000502523.1:p.Gln988=
ENST00000675218.1:c.3922C= (PLCE1)	ENSP00000501910.1:p.Gln1308=
ENST00000675487.1:c.*779C= (PLCE1)	ENSP00000502340.1:n.*779C=
ENST00000675718.1:c.4115C= (PLCE1)
ENST00000676102.1:c.3691C= (PLCE1)	ENSP00000502811.1:p.Gln1231=
ENST00000685253.1:c.*1389C= (PLCE1)	ENSP00000509405.1:n.*1389C=
ENST00000685889.1:n.1581C= (PLCE1)
ENST00000686954.1:c.*130C= (PLCE1)	ENSP00000508416.1:n.*130C=
ENST00000688810.1:c.3874C= (PLCE1)	ENSP00000509140.1:p.Gln1292=
ENST00000689233.1:n.9054C= (PLCE1)
ENST00000690340.1:n.2519C= (PLCE1)
ENST00000692286.1:c.4846C= (PLCE1)	ENSP00000509490.1:p.Gln1616=
ENST00000692396.1:c.4798C= (PLCE1)	ENSP00000508605.1:p.Gln1600=
XM_006717885.2:c.4888C= (PLCE1)	XP_006717948.1:p.Gln1630=
XM_006717885.4:c.4888C= (PLCE1)	XP_006717948.1:p.Gln1630=
XM_006717886.2:c.4888C= (PLCE1)	XP_006717949.1:p.Gln1630=
XM_006717888.2:c.4885C= (PLCE1)	XP_006717951.1:p.Gln1629=
XM_006717888.4:c.4885C= (PLCE1)	XP_006717951.1:p.Gln1629=
XM_006717889.2:c.4840C= (PLCE1)	XP_006717952.1:p.Gln1614=
XM_006717889.4:c.4840C= (PLCE1)	XP_006717952.1:p.Gln1614=
XM_006717890.1:c.3964C= (PLCE1)	XP_006717953.1:p.Gln1322=
XM_006717890.3:c.3964C= (PLCE1)	XP_006717953.1:p.Gln1322=
XM_011539849.1:c.4888C= (PLCE1)	XP_011538151.1:p.Gln1630=
XM_011539849.3:c.4888C= (PLCE1)	XP_011538151.1:p.Gln1630=
XM_011539850.1:c.3733C= (PLCE1)	XP_011538152.1:p.Gln1245=
XM_011539850.3:c.3733C= (PLCE1)	XP_011538152.1:p.Gln1245=
XM_017016310.2:c.4888C= (PLCE1)	XP_016871799.1:p.Gln1630=
XM_017016311.2:c.4888C= (PLCE1)	XP_016871800.1:p.Gln1630=
XM_017016312.2:c.3874C= (PLCE1)	XP_016871801.1:p.Gln1292=