Canonical Allele Identifier: CA470986580

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058324A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298567A>C , CM000672.2:g.94298567A>C	GRCh38
NC_000010.10:g.96058324A>C , CM000672.1:g.96058324A>C	GRCh37
NC_000010.9:g.96048314A>C	NCBI36
NG_015799.1:g.309579A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4432A>C	ENSP00000360426.1:p.Arg1478=
ENST00000685253.1:c.*1899A>C	ENSP00000509405.1:n.*1899A>C
ENST00000685889.1:n.2091A>C
ENST00000686807.1:n.775A>C
ENST00000686954.1:c.*640A>C	ENSP00000508416.1:n.*640A>C
ENST00000688810.1:c.4384A>C	ENSP00000509140.1:p.Arg1462=
ENST00000689233.1:n.9564A>C
ENST00000690340.1:n.3029A>C
ENST00000692286.1:c.5224A>C	ENSP00000509490.1:p.Arg1742=
ENST00000692396.1:c.5308A>C	ENSP00000508605.1:p.Arg1770=
ENST00000371380.8:c.5356A>C MANE Select	ENSP00000360431.2:p.Arg1786=
ENST00000371385.8:c.4330A>C	ENSP00000360438.4:p.Arg1444=
ENST00000674738.1:c.3911A>C
ENST00000674827.1:c.3472A>C	ENSP00000502523.1:p.Arg1158=
ENST00000675218.1:c.4432A>C	ENSP00000501910.1:p.Arg1478=
ENST00000675487.1:c.*1289A>C	ENSP00000502340.1:n.*1289A>C
ENST00000675718.1:c.4625A>C
ENST00000260766.7:c.5356A>C	ENSP00000260766.3:p.Arg1786=
ENST00000371375.1:c.4432A>C	ENSP00000360426.1:p.Arg1478=
ENST00000371380.7:c.5356A>C	ENSP00000360431.2:p.Arg1786=
ENST00000371385.7:c.4432A>C	ENSP00000360438.3:p.Arg1478=
NM_001165979.2:c.4432A>C	NP_001159451.1:p.Arg1478=
NM_001288989.1:c.5308A>C	NP_001275918.1:p.Arg1770=
NM_016341.3:c.5356A>C	NP_057425.3:p.Arg1786=
XM_006717885.2:c.5398A>C	XP_006717948.1:p.Arg1800=
XM_006717886.2:c.5398A>C	XP_006717949.1:p.Arg1800=
XM_006717888.2:c.5395A>C	XP_006717951.1:p.Arg1799=
XM_006717889.2:c.5350A>C	XP_006717952.1:p.Arg1784=
XM_006717890.1:c.4474A>C	XP_006717953.1:p.Arg1492=
XM_011539849.1:c.5398A>C	XP_011538151.1:p.Arg1800=
XM_011539850.1:c.4243A>C	XP_011538152.1:p.Arg1415=
XM_006717885.4:c.5398A>C	XP_006717948.1:p.Arg1800=
XM_006717888.4:c.5395A>C	XP_006717951.1:p.Arg1799=
XM_006717889.4:c.5350A>C	XP_006717952.1:p.Arg1784=
XM_006717890.3:c.4474A>C	XP_006717953.1:p.Arg1492=
XM_011539849.3:c.5398A>C	XP_011538151.1:p.Arg1800=
XM_011539850.3:c.4243A>C	XP_011538152.1:p.Arg1415=
XM_017016310.2:c.5398A>C	XP_016871799.1:p.Arg1800=
XM_017016311.2:c.5398A>C	XP_016871800.1:p.Arg1800=
XM_017016312.2:c.4384A>C	XP_016871801.1:p.Arg1462=
NM_001288989.2:c.5308A>C	NP_001275918.1:p.Arg1770=
NM_016341.4:c.5356A>C MANE Select	NP_057425.3:p.Arg1786=