Canonical Allele Identifier: CA377641706

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058163G>A (hg19) ; chr10:g.94298406G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4271G>A	ENSP00000360426.1:p.Trp1424Ter
ENST00000685253.1:c.*1738G>A	ENSP00000509405.1:n.*1738G>A
ENST00000685889.1:n.1930G>A
ENST00000686807.1:n.614G>A
ENST00000686954.1:c.*479G>A	ENSP00000508416.1:n.*479G>A
ENST00000688810.1:c.4223G>A	ENSP00000509140.1:p.Trp1408Ter
ENST00000689233.1:n.9403G>A
ENST00000690340.1:n.2868G>A
ENST00000692286.1:c.5063G>A	ENSP00000509490.1:p.Trp1688Ter
ENST00000692396.1:c.5147G>A	ENSP00000508605.1:p.Trp1716Ter
ENST00000371380.8:c.5195G>A MANE Select	ENSP00000360431.2:p.Trp1732Ter
ENST00000371385.8:c.4169G>A	ENSP00000360438.4:p.Trp1390Ter
ENST00000674738.1:c.3750G>A
ENST00000674827.1:c.3311G>A	ENSP00000502523.1:p.Trp1104Ter
ENST00000675218.1:c.4271G>A	ENSP00000501910.1:p.Trp1424Ter
ENST00000675487.1:c.*1128G>A	ENSP00000502340.1:n.*1128G>A
ENST00000675718.1:c.4464G>A
ENST00000676102.1:c.4040G>A	ENSP00000502811.1:p.Trp1347Ter
ENST00000260766.7:c.5195G>A	ENSP00000260766.3:p.Trp1732Ter
ENST00000371375.1:c.4271G>A	ENSP00000360426.1:p.Trp1424Ter
ENST00000371380.7:c.5195G>A	ENSP00000360431.2:p.Trp1732Ter
ENST00000371385.7:c.4271G>A	ENSP00000360438.3:p.Trp1424Ter
NM_001165979.2:c.4271G>A	NP_001159451.1:p.Trp1424Ter
NM_001288989.1:c.5147G>A	NP_001275918.1:p.Trp1716Ter
NM_016341.3:c.5195G>A	NP_057425.3:p.Trp1732Ter
XM_006717885.2:c.5237G>A	XP_006717948.1:p.Trp1746Ter
XM_006717886.2:c.5237G>A	XP_006717949.1:p.Trp1746Ter
XM_006717888.2:c.5234G>A	XP_006717951.1:p.Trp1745Ter
XM_006717889.2:c.5189G>A	XP_006717952.1:p.Trp1730Ter
XM_006717890.1:c.4313G>A	XP_006717953.1:p.Trp1438Ter
XM_011539849.1:c.5237G>A	XP_011538151.1:p.Trp1746Ter
XM_011539850.1:c.4082G>A	XP_011538152.1:p.Trp1361Ter
XM_006717885.4:c.5237G>A	XP_006717948.1:p.Trp1746Ter
XM_006717888.4:c.5234G>A	XP_006717951.1:p.Trp1745Ter
XM_006717889.4:c.5189G>A	XP_006717952.1:p.Trp1730Ter
XM_006717890.3:c.4313G>A	XP_006717953.1:p.Trp1438Ter
XM_011539849.3:c.5237G>A	XP_011538151.1:p.Trp1746Ter
XM_011539850.3:c.4082G>A	XP_011538152.1:p.Trp1361Ter
XM_017016310.2:c.5237G>A	XP_016871799.1:p.Trp1746Ter
XM_017016311.2:c.5237G>A	XP_016871800.1:p.Trp1746Ter
XM_017016312.2:c.4223G>A	XP_016871801.1:p.Trp1408Ter
NM_001288989.2:c.5147G>A	NP_001275918.1:p.Trp1716Ter
NM_016341.4:c.5195G>A MANE Select	NP_057425.3:p.Trp1732Ter