Canonical Allele Identifier: CA377648338

Gene: PLCE1 NOC3L

Linked Data

• dbSNP Id: rs1361352223
• gnomAD v2: 10-96081742-G-A
• MyVariant Identifiers: chr10:g.96081742G>A (hg19) ; chr10:g.94321985G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94321985G>A , CM000672.2:g.94321985G>A	GRCh38
NC_000010.10:g.96081742G>A , CM000672.1:g.96081742G>A	GRCh37
NC_000010.9:g.96071732G>A	NCBI36
NG_015799.1:g.332997G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.5503G>A (PLCE1)	ENSP00000360426.1:p.Asp1835Asn
ENST00000685132.1:n.3826G>A (PLCE1)
ENST00000685253.1:c.*2970G>A (PLCE1)	ENSP00000509405.1:n.*2970G>A
ENST00000685889.1:n.3162G>A (PLCE1)
ENST00000686807.1:n.1846G>A (PLCE1)
ENST00000686954.1:c.*1711G>A (PLCE1)	ENSP00000508416.1:n.*1711G>A
ENST00000688810.1:c.5455G>A (PLCE1)	ENSP00000509140.1:p.Asp1819Asn
ENST00000689233.1:n.10635G>A (PLCE1)
ENST00000690340.1:n.4100G>A (PLCE1)
ENST00000692286.1:c.6295G>A (PLCE1)	ENSP00000509490.1:p.Asp2099Asn
ENST00000692396.1:c.6379G>A (PLCE1)	ENSP00000508605.1:p.Asp2127Asn
ENST00000371380.8:c.6427G>A (PLCE1) MANE Select	ENSP00000360431.2:p.Asp2143Asn
ENST00000371385.8:c.5401G>A (PLCE1)	ENSP00000360438.4:p.Asp1801Asn
ENST00000674738.1:c.4982G>A (PLCE1)
ENST00000674827.1:c.4543G>A (PLCE1)	ENSP00000502523.1:p.Asp1515Asn
ENST00000675218.1:c.5503G>A (PLCE1)	ENSP00000501910.1:p.Asp1835Asn
ENST00000675487.1:c.*2360G>A (PLCE1)	ENSP00000502340.1:n.*2360G>A
ENST00000675718.1:c.5696G>A (PLCE1)
ENST00000260766.7:c.6427G>A (PLCE1)	ENSP00000260766.3:p.Asp2143Asn
ENST00000371375.1:c.5503G>A (PLCE1)	ENSP00000360426.1:p.Asp1835Asn
ENST00000371380.7:c.6427G>A (PLCE1)	ENSP00000360431.2:p.Asp2143Asn
ENST00000371385.7:c.5503G>A (PLCE1)	ENSP00000360438.3:p.Asp1835Asn
NM_001165979.2:c.5503G>A (PLCE1)	NP_001159451.1:p.Asp1835Asn
NM_001288989.1:c.6379G>A (PLCE1)	NP_001275918.1:p.Asp2127Asn
NM_016341.3:c.6427G>A (PLCE1)	NP_057425.3:p.Asp2143Asn
XM_006717885.2:c.6469G>A (PLCE1)	XP_006717948.1:p.Asp2157Asn
XM_006717886.2:c.6469G>A (PLCE1)	XP_006717949.1:p.Asp2157Asn
XM_006717888.2:c.6466G>A (PLCE1)	XP_006717951.1:p.Asp2156Asn
XM_006717889.2:c.6421G>A (PLCE1)	XP_006717952.1:p.Asp2141Asn
XM_006717890.1:c.5545G>A (PLCE1)	XP_006717953.1:p.Asp1849Asn
XM_011539849.1:c.6469G>A (PLCE1)	XP_011538151.1:p.Asp2157Asn
XM_011539850.1:c.5314G>A (PLCE1)	XP_011538152.1:p.Asp1772Asn
XR_945799.1:n.3311-6521C>T (NOC3L)
XM_006717885.4:c.6469G>A (PLCE1)	XP_006717948.1:p.Asp2157Asn
XM_006717888.4:c.6466G>A (PLCE1)	XP_006717951.1:p.Asp2156Asn
XM_006717889.4:c.6421G>A (PLCE1)	XP_006717952.1:p.Asp2141Asn
XM_006717890.3:c.5545G>A (PLCE1)	XP_006717953.1:p.Asp1849Asn
XM_011539849.3:c.6469G>A (PLCE1)	XP_011538151.1:p.Asp2157Asn
XM_011539850.3:c.5314G>A (PLCE1)	XP_011538152.1:p.Asp1772Asn
XM_017016310.2:c.6469G>A (PLCE1)	XP_016871799.1:p.Asp2157Asn
XM_017016311.2:c.6469G>A (PLCE1)	XP_016871800.1:p.Asp2157Asn
XM_017016312.2:c.5455G>A (PLCE1)	XP_016871801.1:p.Asp1819Asn
XR_002957007.1:n.3312-6521C>T (NOC3L)
NM_001288989.2:c.6379G>A (PLCE1)	NP_001275918.1:p.Asp2127Asn
NM_016341.4:c.6427G>A (PLCE1) MANE Select	NP_057425.3:p.Asp2143Asn