Canonical Allele Identifier: CA377641952

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058277G>C (hg19) ; chr10:g.94298520G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298520G>C , CM000672.2:g.94298520G>C	GRCh38
NC_000010.10:g.96058277G>C , CM000672.1:g.96058277G>C	GRCh37
NC_000010.9:g.96048267G>C	NCBI36
NG_015799.1:g.309532G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4385G>C	ENSP00000360426.1:p.Arg1462Pro
ENST00000685253.1:c.*1852G>C	ENSP00000509405.1:n.*1852G>C
ENST00000685889.1:n.2044G>C
ENST00000686807.1:n.728G>C
ENST00000686954.1:c.*593G>C	ENSP00000508416.1:n.*593G>C
ENST00000688810.1:c.4337G>C	ENSP00000509140.1:p.Arg1446Pro
ENST00000689233.1:n.9517G>C
ENST00000690340.1:n.2982G>C
ENST00000692286.1:c.5177G>C	ENSP00000509490.1:p.Arg1726Pro
ENST00000692396.1:c.5261G>C	ENSP00000508605.1:p.Arg1754Pro
ENST00000371380.8:c.5309G>C MANE Select	ENSP00000360431.2:p.Arg1770Pro
ENST00000371385.8:c.4283G>C	ENSP00000360438.4:p.Arg1428Pro
ENST00000674738.1:c.3864G>C
ENST00000674827.1:c.3425G>C	ENSP00000502523.1:p.Arg1142Pro
ENST00000675218.1:c.4385G>C	ENSP00000501910.1:p.Arg1462Pro
ENST00000675487.1:c.*1242G>C	ENSP00000502340.1:n.*1242G>C
ENST00000675718.1:c.4578G>C
ENST00000260766.7:c.5309G>C	ENSP00000260766.3:p.Arg1770Pro
ENST00000371375.1:c.4385G>C	ENSP00000360426.1:p.Arg1462Pro
ENST00000371380.7:c.5309G>C	ENSP00000360431.2:p.Arg1770Pro
ENST00000371385.7:c.4385G>C	ENSP00000360438.3:p.Arg1462Pro
NM_001165979.2:c.4385G>C	NP_001159451.1:p.Arg1462Pro
NM_001288989.1:c.5261G>C	NP_001275918.1:p.Arg1754Pro
NM_016341.3:c.5309G>C	NP_057425.3:p.Arg1770Pro
XM_006717885.2:c.5351G>C	XP_006717948.1:p.Arg1784Pro
XM_006717886.2:c.5351G>C	XP_006717949.1:p.Arg1784Pro
XM_006717888.2:c.5348G>C	XP_006717951.1:p.Arg1783Pro
XM_006717889.2:c.5303G>C	XP_006717952.1:p.Arg1768Pro
XM_006717890.1:c.4427G>C	XP_006717953.1:p.Arg1476Pro
XM_011539849.1:c.5351G>C	XP_011538151.1:p.Arg1784Pro
XM_011539850.1:c.4196G>C	XP_011538152.1:p.Arg1399Pro
XM_006717885.4:c.5351G>C	XP_006717948.1:p.Arg1784Pro
XM_006717888.4:c.5348G>C	XP_006717951.1:p.Arg1783Pro
XM_006717889.4:c.5303G>C	XP_006717952.1:p.Arg1768Pro
XM_006717890.3:c.4427G>C	XP_006717953.1:p.Arg1476Pro
XM_011539849.3:c.5351G>C	XP_011538151.1:p.Arg1784Pro
XM_011539850.3:c.4196G>C	XP_011538152.1:p.Arg1399Pro
XM_017016310.2:c.5351G>C	XP_016871799.1:p.Arg1784Pro
XM_017016311.2:c.5351G>C	XP_016871800.1:p.Arg1784Pro
XM_017016312.2:c.4337G>C	XP_016871801.1:p.Arg1446Pro
NM_001288989.2:c.5261G>C	NP_001275918.1:p.Arg1754Pro
NM_016341.4:c.5309G>C MANE Select	NP_057425.3:p.Arg1770Pro