Canonical Allele Identifier: CA377641707

Gene: PLCE1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298406G>C , CM000672.2:g.94298406G>C	GRCh38
NC_000010.10:g.96058163G>C , CM000672.1:g.96058163G>C	GRCh37
NC_000010.9:g.96048153G>C	NCBI36
NG_015799.1:g.309418G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4271G>C	ENSP00000360426.1:p.Trp1424Ser
ENST00000685253.1:c.*1738G>C	ENSP00000509405.1:n.*1738G>C
ENST00000685889.1:n.1930G>C
ENST00000686807.1:n.614G>C
ENST00000686954.1:c.*479G>C	ENSP00000508416.1:n.*479G>C
ENST00000688810.1:c.4223G>C	ENSP00000509140.1:p.Trp1408Ser
ENST00000689233.1:n.9403G>C
ENST00000690340.1:n.2868G>C
ENST00000692286.1:c.5063G>C	ENSP00000509490.1:p.Trp1688Ser
ENST00000692396.1:c.5147G>C	ENSP00000508605.1:p.Trp1716Ser
ENST00000371380.8:c.5195G>C MANE Select	ENSP00000360431.2:p.Trp1732Ser
ENST00000371385.8:c.4169G>C	ENSP00000360438.4:p.Trp1390Ser
ENST00000674738.1:c.3750G>C
ENST00000674827.1:c.3311G>C	ENSP00000502523.1:p.Trp1104Ser
ENST00000675218.1:c.4271G>C	ENSP00000501910.1:p.Trp1424Ser
ENST00000675487.1:c.*1128G>C	ENSP00000502340.1:n.*1128G>C
ENST00000675718.1:c.4464G>C
ENST00000676102.1:c.4040G>C	ENSP00000502811.1:p.Trp1347Ser
ENST00000260766.7:c.5195G>C	ENSP00000260766.3:p.Trp1732Ser
ENST00000371375.1:c.4271G>C	ENSP00000360426.1:p.Trp1424Ser
ENST00000371380.7:c.5195G>C	ENSP00000360431.2:p.Trp1732Ser
ENST00000371385.7:c.4271G>C	ENSP00000360438.3:p.Trp1424Ser
NM_001165979.2:c.4271G>C	NP_001159451.1:p.Trp1424Ser
NM_001288989.1:c.5147G>C	NP_001275918.1:p.Trp1716Ser
NM_016341.3:c.5195G>C	NP_057425.3:p.Trp1732Ser
XM_006717885.2:c.5237G>C	XP_006717948.1:p.Trp1746Ser
XM_006717886.2:c.5237G>C	XP_006717949.1:p.Trp1746Ser
XM_006717888.2:c.5234G>C	XP_006717951.1:p.Trp1745Ser
XM_006717889.2:c.5189G>C	XP_006717952.1:p.Trp1730Ser
XM_006717890.1:c.4313G>C	XP_006717953.1:p.Trp1438Ser
XM_011539849.1:c.5237G>C	XP_011538151.1:p.Trp1746Ser
XM_011539850.1:c.4082G>C	XP_011538152.1:p.Trp1361Ser
XM_006717885.4:c.5237G>C	XP_006717948.1:p.Trp1746Ser
XM_006717888.4:c.5234G>C	XP_006717951.1:p.Trp1745Ser
XM_006717889.4:c.5189G>C	XP_006717952.1:p.Trp1730Ser
XM_006717890.3:c.4313G>C	XP_006717953.1:p.Trp1438Ser
XM_011539849.3:c.5237G>C	XP_011538151.1:p.Trp1746Ser
XM_011539850.3:c.4082G>C	XP_011538152.1:p.Trp1361Ser
XM_017016310.2:c.5237G>C	XP_016871799.1:p.Trp1746Ser
XM_017016311.2:c.5237G>C	XP_016871800.1:p.Trp1746Ser
XM_017016312.2:c.4223G>C	XP_016871801.1:p.Trp1408Ser
NM_001288989.2:c.5147G>C	NP_001275918.1:p.Trp1716Ser
NM_016341.4:c.5195G>C MANE Select	NP_057425.3:p.Trp1732Ser