Canonical Allele Identifier: CA377642705

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96064245C>G (hg19) ; chr10:g.94304488C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94304488C>G , CM000672.2:g.94304488C>G	GRCh38
NC_000010.10:g.96064245C>G , CM000672.1:g.96064245C>G	GRCh37
NC_000010.9:g.96054235C>G	NCBI36
NG_015799.1:g.315500C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4541C>G	ENSP00000360426.1:p.Pro1514Arg
ENST00000685253.1:c.*2008C>G	ENSP00000509405.1:n.*2008C>G
ENST00000685889.1:n.2200C>G
ENST00000686807.1:n.884C>G
ENST00000686954.1:c.*749C>G	ENSP00000508416.1:n.*749C>G
ENST00000688810.1:c.4493C>G	ENSP00000509140.1:p.Pro1498Arg
ENST00000689233.1:n.9673C>G
ENST00000690340.1:n.3138C>G
ENST00000692286.1:c.5333C>G	ENSP00000509490.1:p.Pro1778Arg
ENST00000692396.1:c.5417C>G	ENSP00000508605.1:p.Pro1806Arg
ENST00000371380.8:c.5465C>G MANE Select	ENSP00000360431.2:p.Pro1822Arg
ENST00000371385.8:c.4439C>G	ENSP00000360438.4:p.Pro1480Arg
ENST00000674738.1:c.4020C>G
ENST00000674827.1:c.3581C>G	ENSP00000502523.1:p.Pro1194Arg
ENST00000675218.1:c.4541C>G	ENSP00000501910.1:p.Pro1514Arg
ENST00000675487.1:c.*1398C>G	ENSP00000502340.1:n.*1398C>G
ENST00000675718.1:c.4734C>G
ENST00000260766.7:c.5465C>G	ENSP00000260766.3:p.Pro1822Arg
ENST00000371375.1:c.4541C>G	ENSP00000360426.1:p.Pro1514Arg
ENST00000371380.7:c.5465C>G	ENSP00000360431.2:p.Pro1822Arg
ENST00000371385.7:c.4541C>G	ENSP00000360438.3:p.Pro1514Arg
NM_001165979.2:c.4541C>G	NP_001159451.1:p.Pro1514Arg
NM_001288989.1:c.5417C>G	NP_001275918.1:p.Pro1806Arg
NM_016341.3:c.5465C>G	NP_057425.3:p.Pro1822Arg
XM_006717885.2:c.5507C>G	XP_006717948.1:p.Pro1836Arg
XM_006717886.2:c.5507C>G	XP_006717949.1:p.Pro1836Arg
XM_006717888.2:c.5504C>G	XP_006717951.1:p.Pro1835Arg
XM_006717889.2:c.5459C>G	XP_006717952.1:p.Pro1820Arg
XM_006717890.1:c.4583C>G	XP_006717953.1:p.Pro1528Arg
XM_011539849.1:c.5507C>G	XP_011538151.1:p.Pro1836Arg
XM_011539850.1:c.4352C>G	XP_011538152.1:p.Pro1451Arg
XM_006717885.4:c.5507C>G	XP_006717948.1:p.Pro1836Arg
XM_006717888.4:c.5504C>G	XP_006717951.1:p.Pro1835Arg
XM_006717889.4:c.5459C>G	XP_006717952.1:p.Pro1820Arg
XM_006717890.3:c.4583C>G	XP_006717953.1:p.Pro1528Arg
XM_011539849.3:c.5507C>G	XP_011538151.1:p.Pro1836Arg
XM_011539850.3:c.4352C>G	XP_011538152.1:p.Pro1451Arg
XM_017016310.2:c.5507C>G	XP_016871799.1:p.Pro1836Arg
XM_017016311.2:c.5507C>G	XP_016871800.1:p.Pro1836Arg
XM_017016312.2:c.4493C>G	XP_016871801.1:p.Pro1498Arg
NM_001288989.2:c.5417C>G	NP_001275918.1:p.Pro1806Arg
NM_016341.4:c.5465C>G MANE Select	NP_057425.3:p.Pro1822Arg