Canonical Allele Identifier: CA1929017044

Gene: PLCE1 NOC3L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94322006_94322007delinsCG , CM000672.2:g.94322006_94322007delinsCG	GRCh38
NC_000010.10:g.96081763_96081764delinsCG , CM000672.1:g.96081763_96081764delinsCG	GRCh37
NC_000010.9:g.96071753_96071754delinsCG	NCBI36
NG_015799.1:g.333018_333019delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.5524_5525delinsCG (PLCE1)	ENSP00000360426.1:p.Arg1842=
ENST00000685132.1:n.3847_3848delinsCG (PLCE1)
ENST00000685253.1:c.*2991_*2992delinsCG (PLCE1)	ENSP00000509405.1:n.*2991_*2992delinsCG
ENST00000685889.1:n.3183_3184delinsCG (PLCE1)
ENST00000686807.1:n.1867_1868delinsCG (PLCE1)
ENST00000686954.1:c.*1732_*1733delinsCG (PLCE1)	ENSP00000508416.1:n.*1732_*1733delinsCG
ENST00000688810.1:c.5476_5477delinsCG (PLCE1)	ENSP00000509140.1:p.Arg1826=
ENST00000689233.1:n.10656_10657delinsCG (PLCE1)
ENST00000690340.1:n.4121_4122delinsCG (PLCE1)
ENST00000692286.1:c.6316_6317delinsCG (PLCE1)	ENSP00000509490.1:p.Arg2106=
ENST00000692396.1:c.6400_6401delinsCG (PLCE1)	ENSP00000508605.1:p.Arg2134=
ENST00000371380.8:c.6448_6449delinsCG (PLCE1) MANE Select	ENSP00000360431.2:p.Arg2150=
ENST00000371385.8:c.5422_5423delinsCG (PLCE1)	ENSP00000360438.4:p.Arg1808=
ENST00000674738.1:c.5003_5004delinsCG (PLCE1)
ENST00000674827.1:c.4564_4565delinsCG (PLCE1)	ENSP00000502523.1:p.Arg1522=
ENST00000675218.1:c.5524_5525delinsCG (PLCE1)	ENSP00000501910.1:p.Arg1842=
ENST00000675487.1:c.*2381_*2382delinsCG (PLCE1)	ENSP00000502340.1:n.*2381_*2382delinsCG
ENST00000675718.1:c.5717_5718delinsCG (PLCE1)
ENST00000260766.7:c.6448_6449delinsCG (PLCE1)	ENSP00000260766.3:p.Arg2150=
ENST00000371375.1:c.5524_5525delinsCG (PLCE1)	ENSP00000360426.1:p.Arg1842=
ENST00000371380.7:c.6448_6449delinsCG (PLCE1)	ENSP00000360431.2:p.Arg2150=
ENST00000371385.7:c.5524_5525delinsCG (PLCE1)	ENSP00000360438.3:p.Arg1842=
NM_001165979.2:c.5524_5525delinsCG (PLCE1)	NP_001159451.1:p.Arg1842=
NM_001288989.1:c.6400_6401delinsCG (PLCE1)	NP_001275918.1:p.Arg2134=
NM_016341.3:c.6448_6449delinsCG (PLCE1)	NP_057425.3:p.Arg2150=
XM_006717885.2:c.6490_6491delinsCG (PLCE1)	XP_006717948.1:p.Arg2164=
XM_006717886.2:c.6490_6491delinsCG (PLCE1)	XP_006717949.1:p.Arg2164=
XM_006717888.2:c.6487_6488delinsCG (PLCE1)	XP_006717951.1:p.Arg2163=
XM_006717889.2:c.6442_6443delinsCG (PLCE1)	XP_006717952.1:p.Arg2148=
XM_006717890.1:c.5566_5567delinsCG (PLCE1)	XP_006717953.1:p.Arg1856=
XM_011539849.1:c.6490_6491delinsCG (PLCE1)	XP_011538151.1:p.Arg2164=
XM_011539850.1:c.5335_5336delinsCG (PLCE1)	XP_011538152.1:p.Arg1779=
XR_945799.1:n.3311-6543_3311-6542delinsCG (NOC3L)
XM_006717885.4:c.6490_6491delinsCG (PLCE1)	XP_006717948.1:p.Arg2164=
XM_006717888.4:c.6487_6488delinsCG (PLCE1)	XP_006717951.1:p.Arg2163=
XM_006717889.4:c.6442_6443delinsCG (PLCE1)	XP_006717952.1:p.Arg2148=
XM_006717890.3:c.5566_5567delinsCG (PLCE1)	XP_006717953.1:p.Arg1856=
XM_011539849.3:c.6490_6491delinsCG (PLCE1)	XP_011538151.1:p.Arg2164=
XM_011539850.3:c.5335_5336delinsCG (PLCE1)	XP_011538152.1:p.Arg1779=
XM_017016310.2:c.6490_6491delinsCG (PLCE1)	XP_016871799.1:p.Arg2164=
XM_017016311.2:c.6490_6491delinsCG (PLCE1)	XP_016871800.1:p.Arg2164=
XM_017016312.2:c.5476_5477delinsCG (PLCE1)	XP_016871801.1:p.Arg1826=
XR_002957007.1:n.3312-6543_3312-6542delinsCG (NOC3L)
NM_001288989.2:c.6400_6401delinsCG (PLCE1)	NP_001275918.1:p.Arg2134=
NM_016341.4:c.6448_6449delinsCG (PLCE1) MANE Select	NP_057425.3:p.Arg2150=