Canonical Allele Identifier: CA377642231

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058390G>C (hg19) ; chr10:g.94298633G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298633G>C , CM000672.2:g.94298633G>C	GRCh38
NC_000010.10:g.96058390G>C , CM000672.1:g.96058390G>C	GRCh37
NC_000010.9:g.96048380G>C	NCBI36
NG_015799.1:g.309645G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4498G>C	ENSP00000360426.1:p.Gly1500Arg
ENST00000685253.1:c.*1965G>C	ENSP00000509405.1:n.*1965G>C
ENST00000685889.1:n.2157G>C
ENST00000686807.1:n.841G>C
ENST00000686954.1:c.*706G>C	ENSP00000508416.1:n.*706G>C
ENST00000688810.1:c.4450G>C	ENSP00000509140.1:p.Gly1484Arg
ENST00000689233.1:n.9630G>C
ENST00000690340.1:n.3095G>C
ENST00000692286.1:c.5290G>C	ENSP00000509490.1:p.Gly1764Arg
ENST00000692396.1:c.5374G>C	ENSP00000508605.1:p.Gly1792Arg
ENST00000371380.8:c.5422G>C MANE Select	ENSP00000360431.2:p.Gly1808Arg
ENST00000371385.8:c.4396G>C	ENSP00000360438.4:p.Gly1466Arg
ENST00000674738.1:c.3977G>C
ENST00000674827.1:c.3538G>C	ENSP00000502523.1:p.Gly1180Arg
ENST00000675218.1:c.4498G>C	ENSP00000501910.1:p.Gly1500Arg
ENST00000675487.1:c.*1355G>C	ENSP00000502340.1:n.*1355G>C
ENST00000675718.1:c.4691G>C
ENST00000260766.7:c.5422G>C	ENSP00000260766.3:p.Gly1808Arg
ENST00000371375.1:c.4498G>C	ENSP00000360426.1:p.Gly1500Arg
ENST00000371380.7:c.5422G>C	ENSP00000360431.2:p.Gly1808Arg
ENST00000371385.7:c.4498G>C	ENSP00000360438.3:p.Gly1500Arg
NM_001165979.2:c.4498G>C	NP_001159451.1:p.Gly1500Arg
NM_001288989.1:c.5374G>C	NP_001275918.1:p.Gly1792Arg
NM_016341.3:c.5422G>C	NP_057425.3:p.Gly1808Arg
XM_006717885.2:c.5464G>C	XP_006717948.1:p.Gly1822Arg
XM_006717886.2:c.5464G>C	XP_006717949.1:p.Gly1822Arg
XM_006717888.2:c.5461G>C	XP_006717951.1:p.Gly1821Arg
XM_006717889.2:c.5416G>C	XP_006717952.1:p.Gly1806Arg
XM_006717890.1:c.4540G>C	XP_006717953.1:p.Gly1514Arg
XM_011539849.1:c.5464G>C	XP_011538151.1:p.Gly1822Arg
XM_011539850.1:c.4309G>C	XP_011538152.1:p.Gly1437Arg
XM_006717885.4:c.5464G>C	XP_006717948.1:p.Gly1822Arg
XM_006717888.4:c.5461G>C	XP_006717951.1:p.Gly1821Arg
XM_006717889.4:c.5416G>C	XP_006717952.1:p.Gly1806Arg
XM_006717890.3:c.4540G>C	XP_006717953.1:p.Gly1514Arg
XM_011539849.3:c.5464G>C	XP_011538151.1:p.Gly1822Arg
XM_011539850.3:c.4309G>C	XP_011538152.1:p.Gly1437Arg
XM_017016310.2:c.5464G>C	XP_016871799.1:p.Gly1822Arg
XM_017016311.2:c.5464G>C	XP_016871800.1:p.Gly1822Arg
XM_017016312.2:c.4450G>C	XP_016871801.1:p.Gly1484Arg
NM_001288989.2:c.5374G>C	NP_001275918.1:p.Gly1792Arg
NM_016341.4:c.5422G>C MANE Select	NP_057425.3:p.Gly1808Arg