Canonical Allele Identifier: CA377641803

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058210A>C (hg19) ; chr10:g.94298453A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298453A>C , CM000672.2:g.94298453A>C	GRCh38
NC_000010.10:g.96058210A>C , CM000672.1:g.96058210A>C	GRCh37
NC_000010.9:g.96048200A>C	NCBI36
NG_015799.1:g.309465A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4318A>C	ENSP00000360426.1:p.Ile1440Leu
ENST00000685253.1:c.*1785A>C	ENSP00000509405.1:n.*1785A>C
ENST00000685889.1:n.1977A>C
ENST00000686807.1:n.661A>C
ENST00000686954.1:c.*526A>C	ENSP00000508416.1:n.*526A>C
ENST00000688810.1:c.4270A>C	ENSP00000509140.1:p.Ile1424Leu
ENST00000689233.1:n.9450A>C
ENST00000690340.1:n.2915A>C
ENST00000692286.1:c.5110A>C	ENSP00000509490.1:p.Ile1704Leu
ENST00000692396.1:c.5194A>C	ENSP00000508605.1:p.Ile1732Leu
ENST00000371380.8:c.5242A>C MANE Select	ENSP00000360431.2:p.Ile1748Leu
ENST00000371385.8:c.4216A>C	ENSP00000360438.4:p.Ile1406Leu
ENST00000674738.1:c.3797A>C
ENST00000674827.1:c.3358A>C	ENSP00000502523.1:p.Ile1120Leu
ENST00000675218.1:c.4318A>C	ENSP00000501910.1:p.Ile1440Leu
ENST00000675487.1:c.*1175A>C	ENSP00000502340.1:n.*1175A>C
ENST00000675718.1:c.4511A>C
ENST00000676102.1:c.4087A>C	ENSP00000502811.1:p.Ile1363Leu
ENST00000260766.7:c.5242A>C	ENSP00000260766.3:p.Ile1748Leu
ENST00000371375.1:c.4318A>C	ENSP00000360426.1:p.Ile1440Leu
ENST00000371380.7:c.5242A>C	ENSP00000360431.2:p.Ile1748Leu
ENST00000371385.7:c.4318A>C	ENSP00000360438.3:p.Ile1440Leu
NM_001165979.2:c.4318A>C	NP_001159451.1:p.Ile1440Leu
NM_001288989.1:c.5194A>C	NP_001275918.1:p.Ile1732Leu
NM_016341.3:c.5242A>C	NP_057425.3:p.Ile1748Leu
XM_006717885.2:c.5284A>C	XP_006717948.1:p.Ile1762Leu
XM_006717886.2:c.5284A>C	XP_006717949.1:p.Ile1762Leu
XM_006717888.2:c.5281A>C	XP_006717951.1:p.Ile1761Leu
XM_006717889.2:c.5236A>C	XP_006717952.1:p.Ile1746Leu
XM_006717890.1:c.4360A>C	XP_006717953.1:p.Ile1454Leu
XM_011539849.1:c.5284A>C	XP_011538151.1:p.Ile1762Leu
XM_011539850.1:c.4129A>C	XP_011538152.1:p.Ile1377Leu
XM_006717885.4:c.5284A>C	XP_006717948.1:p.Ile1762Leu
XM_006717888.4:c.5281A>C	XP_006717951.1:p.Ile1761Leu
XM_006717889.4:c.5236A>C	XP_006717952.1:p.Ile1746Leu
XM_006717890.3:c.4360A>C	XP_006717953.1:p.Ile1454Leu
XM_011539849.3:c.5284A>C	XP_011538151.1:p.Ile1762Leu
XM_011539850.3:c.4129A>C	XP_011538152.1:p.Ile1377Leu
XM_017016310.2:c.5284A>C	XP_016871799.1:p.Ile1762Leu
XM_017016311.2:c.5284A>C	XP_016871800.1:p.Ile1762Leu
XM_017016312.2:c.4270A>C	XP_016871801.1:p.Ile1424Leu
NM_001288989.2:c.5194A>C	NP_001275918.1:p.Ile1732Leu
NM_016341.4:c.5242A>C MANE Select	NP_057425.3:p.Ile1748Leu