Canonical Allele Identifier: CA1929017093

Gene: PLCE1 NOC3L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94322040C= , CM000672.2:g.94322040C=	GRCh38
NC_000010.10:g.96081797C= , CM000672.1:g.96081797C=	GRCh37
NC_000010.9:g.96071787C=	NCBI36
NG_015799.1:g.333052C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.5558C= (PLCE1)	ENSP00000360426.1:p.Ala1853=
ENST00000685253.1:c.*3025C= (PLCE1)	ENSP00000509405.1:n.*3025C=
ENST00000685889.1:n.3217C= (PLCE1)
ENST00000686807.1:n.1901C= (PLCE1)
ENST00000686954.1:c.*1766C= (PLCE1)	ENSP00000508416.1:n.*1766C=
ENST00000688810.1:c.5510C= (PLCE1)	ENSP00000509140.1:p.Ala1837=
ENST00000689233.1:n.10690C= (PLCE1)
ENST00000690340.1:n.4155C= (PLCE1)
ENST00000692286.1:c.6350C= (PLCE1)	ENSP00000509490.1:p.Ala2117=
ENST00000692396.1:c.6434C= (PLCE1)	ENSP00000508605.1:p.Ala2145=
ENST00000371380.8:c.6482C= (PLCE1) MANE Select	ENSP00000360431.2:p.Ala2161=
ENST00000371385.8:c.5456C= (PLCE1)	ENSP00000360438.4:p.Ala1819=
ENST00000675218.1:c.5558C= (PLCE1)	ENSP00000501910.1:p.Ala1853=
ENST00000675487.1:c.*2415C= (PLCE1)	ENSP00000502340.1:n.*2415C=
ENST00000260766.7:c.6482C= (PLCE1)	ENSP00000260766.3:p.Ala2161=
ENST00000371375.1:c.5558C= (PLCE1)	ENSP00000360426.1:p.Ala1853=
ENST00000371380.7:c.6482C= (PLCE1)	ENSP00000360431.2:p.Ala2161=
ENST00000371385.7:c.5558C= (PLCE1)	ENSP00000360438.3:p.Ala1853=
NM_001165979.2:c.5558C= (PLCE1)	NP_001159451.1:p.Ala1853=
NM_001288989.1:c.6434C= (PLCE1)	NP_001275918.1:p.Ala2145=
NM_016341.3:c.6482C= (PLCE1)	NP_057425.3:p.Ala2161=
XM_006717885.2:c.6524C= (PLCE1)	XP_006717948.1:p.Ala2175=
XM_006717886.2:c.6524C= (PLCE1)	XP_006717949.1:p.Ala2175=
XM_006717888.2:c.6521C= (PLCE1)	XP_006717951.1:p.Ala2174=
XM_006717889.2:c.6476C= (PLCE1)	XP_006717952.1:p.Ala2159=
XM_006717890.1:c.5600C= (PLCE1)	XP_006717953.1:p.Ala1867=
XM_011539849.1:c.6524C= (PLCE1)	XP_011538151.1:p.Ala2175=
XM_011539850.1:c.5369C= (PLCE1)	XP_011538152.1:p.Ala1790=
XR_945799.1:n.3311-6576G= (NOC3L)
XM_006717885.4:c.6524C= (PLCE1)	XP_006717948.1:p.Ala2175=
XM_006717888.4:c.6521C= (PLCE1)	XP_006717951.1:p.Ala2174=
XM_006717889.4:c.6476C= (PLCE1)	XP_006717952.1:p.Ala2159=
XM_006717890.3:c.5600C= (PLCE1)	XP_006717953.1:p.Ala1867=
XM_011539849.3:c.6524C= (PLCE1)	XP_011538151.1:p.Ala2175=
XM_011539850.3:c.5369C= (PLCE1)	XP_011538152.1:p.Ala1790=
XM_017016310.2:c.6524C= (PLCE1)	XP_016871799.1:p.Ala2175=
XM_017016311.2:c.6524C= (PLCE1)	XP_016871800.1:p.Ala2175=
XM_017016312.2:c.5510C= (PLCE1)	XP_016871801.1:p.Ala1837=
XR_002957007.1:n.3312-6576G= (NOC3L)
NM_001288989.2:c.6434C= (PLCE1)	NP_001275918.1:p.Ala2145=
NM_016341.4:c.6482C= (PLCE1) MANE Select	NP_057425.3:p.Ala2161=