Canonical Allele Identifier: CA470812259

Gene: PLCE1 NOC3L

Linked Data

• MyVariant Identifiers: chr10:g.96081681T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94321924T>A , CM000672.2:g.94321924T>A	GRCh38
NC_000010.10:g.96081681T>A , CM000672.1:g.96081681T>A	GRCh37
NC_000010.9:g.96071671T>A	NCBI36
NG_015799.1:g.332936T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.5442T>A (PLCE1)	ENSP00000360426.1:p.Val1814=
ENST00000685132.1:n.3765T>A (PLCE1)
ENST00000685253.1:c.*2909T>A (PLCE1)	ENSP00000509405.1:n.*2909T>A
ENST00000685889.1:n.3101T>A (PLCE1)
ENST00000686807.1:n.1785T>A (PLCE1)
ENST00000686954.1:c.*1650T>A (PLCE1)	ENSP00000508416.1:n.*1650T>A
ENST00000688810.1:c.5394T>A (PLCE1)	ENSP00000509140.1:p.Val1798=
ENST00000689233.1:n.10574T>A (PLCE1)
ENST00000690340.1:n.4039T>A (PLCE1)
ENST00000692286.1:c.6234T>A (PLCE1)	ENSP00000509490.1:p.Val2078=
ENST00000692396.1:c.6318T>A (PLCE1)	ENSP00000508605.1:p.Val2106=
ENST00000371380.8:c.6366T>A (PLCE1) MANE Select	ENSP00000360431.2:p.Val2122=
ENST00000371385.8:c.5340T>A (PLCE1)	ENSP00000360438.4:p.Val1780=
ENST00000674738.1:c.4921T>A (PLCE1)
ENST00000674827.1:c.4482T>A (PLCE1)	ENSP00000502523.1:p.Val1494=
ENST00000675218.1:c.5442T>A (PLCE1)	ENSP00000501910.1:p.Val1814=
ENST00000675487.1:c.*2299T>A (PLCE1)	ENSP00000502340.1:n.*2299T>A
ENST00000675718.1:c.5635T>A (PLCE1)
ENST00000260766.7:c.6366T>A (PLCE1)	ENSP00000260766.3:p.Val2122=
ENST00000371375.1:c.5442T>A (PLCE1)	ENSP00000360426.1:p.Val1814=
ENST00000371380.7:c.6366T>A (PLCE1)	ENSP00000360431.2:p.Val2122=
ENST00000371385.7:c.5442T>A (PLCE1)	ENSP00000360438.3:p.Val1814=
NM_001165979.2:c.5442T>A (PLCE1)	NP_001159451.1:p.Val1814=
NM_001288989.1:c.6318T>A (PLCE1)	NP_001275918.1:p.Val2106=
NM_016341.3:c.6366T>A (PLCE1)	NP_057425.3:p.Val2122=
XM_006717885.2:c.6408T>A (PLCE1)	XP_006717948.1:p.Val2136=
XM_006717886.2:c.6408T>A (PLCE1)	XP_006717949.1:p.Val2136=
XM_006717888.2:c.6405T>A (PLCE1)	XP_006717951.1:p.Val2135=
XM_006717889.2:c.6360T>A (PLCE1)	XP_006717952.1:p.Val2120=
XM_006717890.1:c.5484T>A (PLCE1)	XP_006717953.1:p.Val1828=
XM_011539849.1:c.6408T>A (PLCE1)	XP_011538151.1:p.Val2136=
XM_011539850.1:c.5253T>A (PLCE1)	XP_011538152.1:p.Val1751=
XR_945799.1:n.3311-6460A>T (NOC3L)
XM_006717885.4:c.6408T>A (PLCE1)	XP_006717948.1:p.Val2136=
XM_006717888.4:c.6405T>A (PLCE1)	XP_006717951.1:p.Val2135=
XM_006717889.4:c.6360T>A (PLCE1)	XP_006717952.1:p.Val2120=
XM_006717890.3:c.5484T>A (PLCE1)	XP_006717953.1:p.Val1828=
XM_011539849.3:c.6408T>A (PLCE1)	XP_011538151.1:p.Val2136=
XM_011539850.3:c.5253T>A (PLCE1)	XP_011538152.1:p.Val1751=
XM_017016310.2:c.6408T>A (PLCE1)	XP_016871799.1:p.Val2136=
XM_017016311.2:c.6408T>A (PLCE1)	XP_016871800.1:p.Val2136=
XM_017016312.2:c.5394T>A (PLCE1)	XP_016871801.1:p.Val1798=
XR_002957007.1:n.3312-6460A>T (NOC3L)
NM_001288989.2:c.6318T>A (PLCE1)	NP_001275918.1:p.Val2106=
NM_016341.4:c.6366T>A (PLCE1) MANE Select	NP_057425.3:p.Val2122=