Canonical Allele Identifier: CA470986572

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058320G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298563G>C , CM000672.2:g.94298563G>C	GRCh38
NC_000010.10:g.96058320G>C , CM000672.1:g.96058320G>C	GRCh37
NC_000010.9:g.96048310G>C	NCBI36
NG_015799.1:g.309575G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4428G>C	ENSP00000360426.1:p.Leu1476=
ENST00000685253.1:c.*1895G>C	ENSP00000509405.1:n.*1895G>C
ENST00000685889.1:n.2087G>C
ENST00000686807.1:n.771G>C
ENST00000686954.1:c.*636G>C	ENSP00000508416.1:n.*636G>C
ENST00000688810.1:c.4380G>C	ENSP00000509140.1:p.Leu1460=
ENST00000689233.1:n.9560G>C
ENST00000690340.1:n.3025G>C
ENST00000692286.1:c.5220G>C	ENSP00000509490.1:p.Leu1740=
ENST00000692396.1:c.5304G>C	ENSP00000508605.1:p.Leu1768=
ENST00000371380.8:c.5352G>C MANE Select	ENSP00000360431.2:p.Leu1784=
ENST00000371385.8:c.4326G>C	ENSP00000360438.4:p.Leu1442=
ENST00000674738.1:c.3907G>C
ENST00000674827.1:c.3468G>C	ENSP00000502523.1:p.Leu1156=
ENST00000675218.1:c.4428G>C	ENSP00000501910.1:p.Leu1476=
ENST00000675487.1:c.*1285G>C	ENSP00000502340.1:n.*1285G>C
ENST00000675718.1:c.4621G>C
ENST00000260766.7:c.5352G>C	ENSP00000260766.3:p.Leu1784=
ENST00000371375.1:c.4428G>C	ENSP00000360426.1:p.Leu1476=
ENST00000371380.7:c.5352G>C	ENSP00000360431.2:p.Leu1784=
ENST00000371385.7:c.4428G>C	ENSP00000360438.3:p.Leu1476=
NM_001165979.2:c.4428G>C	NP_001159451.1:p.Leu1476=
NM_001288989.1:c.5304G>C	NP_001275918.1:p.Leu1768=
NM_016341.3:c.5352G>C	NP_057425.3:p.Leu1784=
XM_006717885.2:c.5394G>C	XP_006717948.1:p.Leu1798=
XM_006717886.2:c.5394G>C	XP_006717949.1:p.Leu1798=
XM_006717888.2:c.5391G>C	XP_006717951.1:p.Leu1797=
XM_006717889.2:c.5346G>C	XP_006717952.1:p.Leu1782=
XM_006717890.1:c.4470G>C	XP_006717953.1:p.Leu1490=
XM_011539849.1:c.5394G>C	XP_011538151.1:p.Leu1798=
XM_011539850.1:c.4239G>C	XP_011538152.1:p.Leu1413=
XM_006717885.4:c.5394G>C	XP_006717948.1:p.Leu1798=
XM_006717888.4:c.5391G>C	XP_006717951.1:p.Leu1797=
XM_006717889.4:c.5346G>C	XP_006717952.1:p.Leu1782=
XM_006717890.3:c.4470G>C	XP_006717953.1:p.Leu1490=
XM_011539849.3:c.5394G>C	XP_011538151.1:p.Leu1798=
XM_011539850.3:c.4239G>C	XP_011538152.1:p.Leu1413=
XM_017016310.2:c.5394G>C	XP_016871799.1:p.Leu1798=
XM_017016311.2:c.5394G>C	XP_016871800.1:p.Leu1798=
XM_017016312.2:c.4380G>C	XP_016871801.1:p.Leu1460=
NM_001288989.2:c.5304G>C	NP_001275918.1:p.Leu1768=
NM_016341.4:c.5352G>C MANE Select	NP_057425.3:p.Leu1784=