Canonical Allele Identifier: CA377640756

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053345G>C (hg19) ; chr10:g.94293588G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293588G>C , CM000672.2:g.94293588G>C	GRCh38
NC_000010.10:g.96053345G>C , CM000672.1:g.96053345G>C	GRCh37
NC_000010.9:g.96043335G>C	NCBI36
NG_015799.1:g.304600G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4192G>C	ENSP00000360426.1:p.Gly1398Arg
ENST00000685253.1:c.*1659G>C	ENSP00000509405.1:n.*1659G>C
ENST00000685889.1:n.1851G>C
ENST00000686807.1:n.535G>C
ENST00000686954.1:c.*400G>C	ENSP00000508416.1:n.*400G>C
ENST00000688810.1:c.4144G>C	ENSP00000509140.1:p.Gly1382Arg
ENST00000689233.1:n.9324G>C
ENST00000690340.1:n.2789G>C
ENST00000692286.1:c.5036-4791G>C	ENSP00000509490.1:n.5036-4791G>C
ENST00000692396.1:c.5068G>C	ENSP00000508605.1:p.Gly1690Arg
ENST00000371380.8:c.5116G>C MANE Select	ENSP00000360431.2:p.Gly1706Arg
ENST00000371385.8:c.4090G>C	ENSP00000360438.4:p.Gly1364Arg
ENST00000674738.1:c.3671G>C
ENST00000674827.1:c.3232G>C	ENSP00000502523.1:p.Gly1078Arg
ENST00000675218.1:c.4192G>C	ENSP00000501910.1:p.Gly1398Arg
ENST00000675487.1:c.*1049G>C	ENSP00000502340.1:n.*1049G>C
ENST00000675718.1:c.4385G>C
ENST00000676102.1:c.3961G>C	ENSP00000502811.1:p.Gly1321Arg
ENST00000260766.7:c.5116G>C	ENSP00000260766.3:p.Gly1706Arg
ENST00000371375.1:c.4192G>C	ENSP00000360426.1:p.Gly1398Arg
ENST00000371380.7:c.5116G>C	ENSP00000360431.2:p.Gly1706Arg
ENST00000371385.7:c.4192G>C	ENSP00000360438.3:p.Gly1398Arg
NM_001165979.2:c.4192G>C	NP_001159451.1:p.Gly1398Arg
NM_001288989.1:c.5068G>C	NP_001275918.1:p.Gly1690Arg
NM_016341.3:c.5116G>C	NP_057425.3:p.Gly1706Arg
XM_006717885.2:c.5158G>C	XP_006717948.1:p.Gly1720Arg
XM_006717886.2:c.5158G>C	XP_006717949.1:p.Gly1720Arg
XM_006717888.2:c.5155G>C	XP_006717951.1:p.Gly1719Arg
XM_006717889.2:c.5110G>C	XP_006717952.1:p.Gly1704Arg
XM_006717890.1:c.4234G>C	XP_006717953.1:p.Gly1412Arg
XM_011539849.1:c.5158G>C	XP_011538151.1:p.Gly1720Arg
XM_011539850.1:c.4003G>C	XP_011538152.1:p.Gly1335Arg
XM_006717885.4:c.5158G>C	XP_006717948.1:p.Gly1720Arg
XM_006717888.4:c.5155G>C	XP_006717951.1:p.Gly1719Arg
XM_006717889.4:c.5110G>C	XP_006717952.1:p.Gly1704Arg
XM_006717890.3:c.4234G>C	XP_006717953.1:p.Gly1412Arg
XM_011539849.3:c.5158G>C	XP_011538151.1:p.Gly1720Arg
XM_011539850.3:c.4003G>C	XP_011538152.1:p.Gly1335Arg
XM_017016310.2:c.5158G>C	XP_016871799.1:p.Gly1720Arg
XM_017016311.2:c.5158G>C	XP_016871800.1:p.Gly1720Arg
XM_017016312.2:c.4144G>C	XP_016871801.1:p.Gly1382Arg
NM_001288989.2:c.5068G>C	NP_001275918.1:p.Gly1690Arg
NM_016341.4:c.5116G>C MANE Select	NP_057425.3:p.Gly1706Arg