Canonical Allele Identifier: CA470812268

Gene: PLCE1 NOC3L

Linked Data

• MyVariant Identifiers: chr10:g.96081702C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94321945C>T , CM000672.2:g.94321945C>T	GRCh38
NC_000010.10:g.96081702C>T , CM000672.1:g.96081702C>T	GRCh37
NC_000010.9:g.96071692C>T	NCBI36
NG_015799.1:g.332957C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.5463C>T (PLCE1)	ENSP00000360426.1:p.Ile1821=
ENST00000685132.1:n.3786C>T (PLCE1)
ENST00000685253.1:c.*2930C>T (PLCE1)	ENSP00000509405.1:n.*2930C>T
ENST00000685889.1:n.3122C>T (PLCE1)
ENST00000686807.1:n.1806C>T (PLCE1)
ENST00000686954.1:c.*1671C>T (PLCE1)	ENSP00000508416.1:n.*1671C>T
ENST00000688810.1:c.5415C>T (PLCE1)	ENSP00000509140.1:p.Ile1805=
ENST00000689233.1:n.10595C>T (PLCE1)
ENST00000690340.1:n.4060C>T (PLCE1)
ENST00000692286.1:c.6255C>T (PLCE1)	ENSP00000509490.1:p.Ile2085=
ENST00000692396.1:c.6339C>T (PLCE1)	ENSP00000508605.1:p.Ile2113=
ENST00000371380.8:c.6387C>T (PLCE1) MANE Select	ENSP00000360431.2:p.Ile2129=
ENST00000371385.8:c.5361C>T (PLCE1)	ENSP00000360438.4:p.Ile1787=
ENST00000674738.1:c.4942C>T (PLCE1)
ENST00000674827.1:c.4503C>T (PLCE1)	ENSP00000502523.1:p.Ile1501=
ENST00000675218.1:c.5463C>T (PLCE1)	ENSP00000501910.1:p.Ile1821=
ENST00000675487.1:c.*2320C>T (PLCE1)	ENSP00000502340.1:n.*2320C>T
ENST00000675718.1:c.5656C>T (PLCE1)
ENST00000260766.7:c.6387C>T (PLCE1)	ENSP00000260766.3:p.Ile2129=
ENST00000371375.1:c.5463C>T (PLCE1)	ENSP00000360426.1:p.Ile1821=
ENST00000371380.7:c.6387C>T (PLCE1)	ENSP00000360431.2:p.Ile2129=
ENST00000371385.7:c.5463C>T (PLCE1)	ENSP00000360438.3:p.Ile1821=
NM_001165979.2:c.5463C>T (PLCE1)	NP_001159451.1:p.Ile1821=
NM_001288989.1:c.6339C>T (PLCE1)	NP_001275918.1:p.Ile2113=
NM_016341.3:c.6387C>T (PLCE1)	NP_057425.3:p.Ile2129=
XM_006717885.2:c.6429C>T (PLCE1)	XP_006717948.1:p.Ile2143=
XM_006717886.2:c.6429C>T (PLCE1)	XP_006717949.1:p.Ile2143=
XM_006717888.2:c.6426C>T (PLCE1)	XP_006717951.1:p.Ile2142=
XM_006717889.2:c.6381C>T (PLCE1)	XP_006717952.1:p.Ile2127=
XM_006717890.1:c.5505C>T (PLCE1)	XP_006717953.1:p.Ile1835=
XM_011539849.1:c.6429C>T (PLCE1)	XP_011538151.1:p.Ile2143=
XM_011539850.1:c.5274C>T (PLCE1)	XP_011538152.1:p.Ile1758=
XR_945799.1:n.3311-6481G>A (NOC3L)
XM_006717885.4:c.6429C>T (PLCE1)	XP_006717948.1:p.Ile2143=
XM_006717888.4:c.6426C>T (PLCE1)	XP_006717951.1:p.Ile2142=
XM_006717889.4:c.6381C>T (PLCE1)	XP_006717952.1:p.Ile2127=
XM_006717890.3:c.5505C>T (PLCE1)	XP_006717953.1:p.Ile1835=
XM_011539849.3:c.6429C>T (PLCE1)	XP_011538151.1:p.Ile2143=
XM_011539850.3:c.5274C>T (PLCE1)	XP_011538152.1:p.Ile1758=
XM_017016310.2:c.6429C>T (PLCE1)	XP_016871799.1:p.Ile2143=
XM_017016311.2:c.6429C>T (PLCE1)	XP_016871800.1:p.Ile2143=
XM_017016312.2:c.5415C>T (PLCE1)	XP_016871801.1:p.Ile1805=
XR_002957007.1:n.3312-6481G>A (NOC3L)
NM_001288989.2:c.6339C>T (PLCE1)	NP_001275918.1:p.Ile2113=
NM_016341.4:c.6387C>T (PLCE1) MANE Select	NP_057425.3:p.Ile2129=