Canonical Allele Identifier: CA377641664

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058142G>C (hg19) ; chr10:g.94298385G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298385G>C , CM000672.2:g.94298385G>C	GRCh38
NC_000010.10:g.96058142G>C , CM000672.1:g.96058142G>C	GRCh37
NC_000010.9:g.96048132G>C	NCBI36
NG_015799.1:g.309397G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4250G>C	ENSP00000360426.1:p.Cys1417Ser
ENST00000685253.1:c.*1717G>C	ENSP00000509405.1:n.*1717G>C
ENST00000685889.1:n.1909G>C
ENST00000686807.1:n.593G>C
ENST00000686954.1:c.*458G>C	ENSP00000508416.1:n.*458G>C
ENST00000688810.1:c.4202G>C	ENSP00000509140.1:p.Cys1401Ser
ENST00000689233.1:n.9382G>C
ENST00000690340.1:n.2847G>C
ENST00000692286.1:c.5042G>C	ENSP00000509490.1:p.Cys1681Ser
ENST00000692396.1:c.5126G>C	ENSP00000508605.1:p.Cys1709Ser
ENST00000371380.8:c.5174G>C MANE Select	ENSP00000360431.2:p.Cys1725Ser
ENST00000371385.8:c.4148G>C	ENSP00000360438.4:p.Cys1383Ser
ENST00000674738.1:c.3729G>C
ENST00000674827.1:c.3290G>C	ENSP00000502523.1:p.Cys1097Ser
ENST00000675218.1:c.4250G>C	ENSP00000501910.1:p.Cys1417Ser
ENST00000675487.1:c.*1107G>C	ENSP00000502340.1:n.*1107G>C
ENST00000675718.1:c.4443G>C
ENST00000676102.1:c.4019G>C	ENSP00000502811.1:p.Cys1340Ser
ENST00000260766.7:c.5174G>C	ENSP00000260766.3:p.Cys1725Ser
ENST00000371375.1:c.4250G>C	ENSP00000360426.1:p.Cys1417Ser
ENST00000371380.7:c.5174G>C	ENSP00000360431.2:p.Cys1725Ser
ENST00000371385.7:c.4250G>C	ENSP00000360438.3:p.Cys1417Ser
NM_001165979.2:c.4250G>C	NP_001159451.1:p.Cys1417Ser
NM_001288989.1:c.5126G>C	NP_001275918.1:p.Cys1709Ser
NM_016341.3:c.5174G>C	NP_057425.3:p.Cys1725Ser
XM_006717885.2:c.5216G>C	XP_006717948.1:p.Cys1739Ser
XM_006717886.2:c.5216G>C	XP_006717949.1:p.Cys1739Ser
XM_006717888.2:c.5213G>C	XP_006717951.1:p.Cys1738Ser
XM_006717889.2:c.5168G>C	XP_006717952.1:p.Cys1723Ser
XM_006717890.1:c.4292G>C	XP_006717953.1:p.Cys1431Ser
XM_011539849.1:c.5216G>C	XP_011538151.1:p.Cys1739Ser
XM_011539850.1:c.4061G>C	XP_011538152.1:p.Cys1354Ser
XM_006717885.4:c.5216G>C	XP_006717948.1:p.Cys1739Ser
XM_006717888.4:c.5213G>C	XP_006717951.1:p.Cys1738Ser
XM_006717889.4:c.5168G>C	XP_006717952.1:p.Cys1723Ser
XM_006717890.3:c.4292G>C	XP_006717953.1:p.Cys1431Ser
XM_011539849.3:c.5216G>C	XP_011538151.1:p.Cys1739Ser
XM_011539850.3:c.4061G>C	XP_011538152.1:p.Cys1354Ser
XM_017016310.2:c.5216G>C	XP_016871799.1:p.Cys1739Ser
XM_017016311.2:c.5216G>C	XP_016871800.1:p.Cys1739Ser
XM_017016312.2:c.4202G>C	XP_016871801.1:p.Cys1401Ser
NM_001288989.2:c.5126G>C	NP_001275918.1:p.Cys1709Ser
NM_016341.4:c.5174G>C MANE Select	NP_057425.3:p.Cys1725Ser