Canonical Allele Identifier: CA377648113

Gene: PLCE1 NOC3L

Linked Data

• MyVariant Identifiers: chr10:g.96081668A>T (hg19) ; chr10:g.94321911A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94321911A>T , CM000672.2:g.94321911A>T	GRCh38
NC_000010.10:g.96081668A>T , CM000672.1:g.96081668A>T	GRCh37
NC_000010.9:g.96071658A>T	NCBI36
NG_015799.1:g.332923A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.5429A>T (PLCE1)	ENSP00000360426.1:p.Glu1810Val
ENST00000685132.1:n.3752A>T (PLCE1)
ENST00000685253.1:c.*2896A>T (PLCE1)	ENSP00000509405.1:n.*2896A>T
ENST00000685889.1:n.3088A>T (PLCE1)
ENST00000686807.1:n.1772A>T (PLCE1)
ENST00000686954.1:c.*1637A>T (PLCE1)	ENSP00000508416.1:n.*1637A>T
ENST00000688810.1:c.5381A>T (PLCE1)	ENSP00000509140.1:p.Glu1794Val
ENST00000689233.1:n.10561A>T (PLCE1)
ENST00000690340.1:n.4026A>T (PLCE1)
ENST00000692286.1:c.6221A>T (PLCE1)	ENSP00000509490.1:p.Glu2074Val
ENST00000692396.1:c.6305A>T (PLCE1)	ENSP00000508605.1:p.Glu2102Val
ENST00000371380.8:c.6353A>T (PLCE1) MANE Select	ENSP00000360431.2:p.Glu2118Val
ENST00000371385.8:c.5327A>T (PLCE1)	ENSP00000360438.4:p.Glu1776Val
ENST00000674738.1:c.4908A>T (PLCE1)
ENST00000674827.1:c.4469A>T (PLCE1)	ENSP00000502523.1:p.Glu1490Val
ENST00000675218.1:c.5429A>T (PLCE1)	ENSP00000501910.1:p.Glu1810Val
ENST00000675487.1:c.*2286A>T (PLCE1)	ENSP00000502340.1:n.*2286A>T
ENST00000675718.1:c.5622A>T (PLCE1)
ENST00000260766.7:c.6353A>T (PLCE1)	ENSP00000260766.3:p.Glu2118Val
ENST00000371375.1:c.5429A>T (PLCE1)	ENSP00000360426.1:p.Glu1810Val
ENST00000371380.7:c.6353A>T (PLCE1)	ENSP00000360431.2:p.Glu2118Val
ENST00000371385.7:c.5429A>T (PLCE1)	ENSP00000360438.3:p.Glu1810Val
NM_001165979.2:c.5429A>T (PLCE1)	NP_001159451.1:p.Glu1810Val
NM_001288989.1:c.6305A>T (PLCE1)	NP_001275918.1:p.Glu2102Val
NM_016341.3:c.6353A>T (PLCE1)	NP_057425.3:p.Glu2118Val
XM_006717885.2:c.6395A>T (PLCE1)	XP_006717948.1:p.Glu2132Val
XM_006717886.2:c.6395A>T (PLCE1)	XP_006717949.1:p.Glu2132Val
XM_006717888.2:c.6392A>T (PLCE1)	XP_006717951.1:p.Glu2131Val
XM_006717889.2:c.6347A>T (PLCE1)	XP_006717952.1:p.Glu2116Val
XM_006717890.1:c.5471A>T (PLCE1)	XP_006717953.1:p.Glu1824Val
XM_011539849.1:c.6395A>T (PLCE1)	XP_011538151.1:p.Glu2132Val
XM_011539850.1:c.5240A>T (PLCE1)	XP_011538152.1:p.Glu1747Val
XR_945799.1:n.3311-6447T>A (NOC3L)
XM_006717885.4:c.6395A>T (PLCE1)	XP_006717948.1:p.Glu2132Val
XM_006717888.4:c.6392A>T (PLCE1)	XP_006717951.1:p.Glu2131Val
XM_006717889.4:c.6347A>T (PLCE1)	XP_006717952.1:p.Glu2116Val
XM_006717890.3:c.5471A>T (PLCE1)	XP_006717953.1:p.Glu1824Val
XM_011539849.3:c.6395A>T (PLCE1)	XP_011538151.1:p.Glu2132Val
XM_011539850.3:c.5240A>T (PLCE1)	XP_011538152.1:p.Glu1747Val
XM_017016310.2:c.6395A>T (PLCE1)	XP_016871799.1:p.Glu2132Val
XM_017016311.2:c.6395A>T (PLCE1)	XP_016871800.1:p.Glu2132Val
XM_017016312.2:c.5381A>T (PLCE1)	XP_016871801.1:p.Glu1794Val
XR_002957007.1:n.3312-6447T>A (NOC3L)
NM_001288989.2:c.6305A>T (PLCE1)	NP_001275918.1:p.Glu2102Val
NM_016341.4:c.6353A>T (PLCE1) MANE Select	NP_057425.3:p.Glu2118Val