Canonical Allele Identifier: CA377648200

Gene: PLCE1 NOC3L

Linked Data

• MyVariant Identifiers: chr10:g.96081704T>C (hg19) ; chr10:g.94321947T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94321947T>C , CM000672.2:g.94321947T>C	GRCh38
NC_000010.10:g.96081704T>C , CM000672.1:g.96081704T>C	GRCh37
NC_000010.9:g.96071694T>C	NCBI36
NG_015799.1:g.332959T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.5465T>C (PLCE1)	ENSP00000360426.1:p.Leu1822Ser
ENST00000685132.1:n.3788T>C (PLCE1)
ENST00000685253.1:c.*2932T>C (PLCE1)	ENSP00000509405.1:n.*2932T>C
ENST00000685889.1:n.3124T>C (PLCE1)
ENST00000686807.1:n.1808T>C (PLCE1)
ENST00000686954.1:c.*1673T>C (PLCE1)	ENSP00000508416.1:n.*1673T>C
ENST00000688810.1:c.5417T>C (PLCE1)	ENSP00000509140.1:p.Leu1806Ser
ENST00000689233.1:n.10597T>C (PLCE1)
ENST00000690340.1:n.4062T>C (PLCE1)
ENST00000692286.1:c.6257T>C (PLCE1)	ENSP00000509490.1:p.Leu2086Ser
ENST00000692396.1:c.6341T>C (PLCE1)	ENSP00000508605.1:p.Leu2114Ser
ENST00000371380.8:c.6389T>C (PLCE1) MANE Select	ENSP00000360431.2:p.Leu2130Ser
ENST00000371385.8:c.5363T>C (PLCE1)	ENSP00000360438.4:p.Leu1788Ser
ENST00000674738.1:c.4944T>C (PLCE1)
ENST00000674827.1:c.4505T>C (PLCE1)	ENSP00000502523.1:p.Leu1502Ser
ENST00000675218.1:c.5465T>C (PLCE1)	ENSP00000501910.1:p.Leu1822Ser
ENST00000675487.1:c.*2322T>C (PLCE1)	ENSP00000502340.1:n.*2322T>C
ENST00000675718.1:c.5658T>C (PLCE1)
ENST00000260766.7:c.6389T>C (PLCE1)	ENSP00000260766.3:p.Leu2130Ser
ENST00000371375.1:c.5465T>C (PLCE1)	ENSP00000360426.1:p.Leu1822Ser
ENST00000371380.7:c.6389T>C (PLCE1)	ENSP00000360431.2:p.Leu2130Ser
ENST00000371385.7:c.5465T>C (PLCE1)	ENSP00000360438.3:p.Leu1822Ser
NM_001165979.2:c.5465T>C (PLCE1)	NP_001159451.1:p.Leu1822Ser
NM_001288989.1:c.6341T>C (PLCE1)	NP_001275918.1:p.Leu2114Ser
NM_016341.3:c.6389T>C (PLCE1)	NP_057425.3:p.Leu2130Ser
XM_006717885.2:c.6431T>C (PLCE1)	XP_006717948.1:p.Leu2144Ser
XM_006717886.2:c.6431T>C (PLCE1)	XP_006717949.1:p.Leu2144Ser
XM_006717888.2:c.6428T>C (PLCE1)	XP_006717951.1:p.Leu2143Ser
XM_006717889.2:c.6383T>C (PLCE1)	XP_006717952.1:p.Leu2128Ser
XM_006717890.1:c.5507T>C (PLCE1)	XP_006717953.1:p.Leu1836Ser
XM_011539849.1:c.6431T>C (PLCE1)	XP_011538151.1:p.Leu2144Ser
XM_011539850.1:c.5276T>C (PLCE1)	XP_011538152.1:p.Leu1759Ser
XR_945799.1:n.3311-6483A>G (NOC3L)
XM_006717885.4:c.6431T>C (PLCE1)	XP_006717948.1:p.Leu2144Ser
XM_006717888.4:c.6428T>C (PLCE1)	XP_006717951.1:p.Leu2143Ser
XM_006717889.4:c.6383T>C (PLCE1)	XP_006717952.1:p.Leu2128Ser
XM_006717890.3:c.5507T>C (PLCE1)	XP_006717953.1:p.Leu1836Ser
XM_011539849.3:c.6431T>C (PLCE1)	XP_011538151.1:p.Leu2144Ser
XM_011539850.3:c.5276T>C (PLCE1)	XP_011538152.1:p.Leu1759Ser
XM_017016310.2:c.6431T>C (PLCE1)	XP_016871799.1:p.Leu2144Ser
XM_017016311.2:c.6431T>C (PLCE1)	XP_016871800.1:p.Leu2144Ser
XM_017016312.2:c.5417T>C (PLCE1)	XP_016871801.1:p.Leu1806Ser
XR_002957007.1:n.3312-6483A>G (NOC3L)
NM_001288989.2:c.6341T>C (PLCE1)	NP_001275918.1:p.Leu2114Ser
NM_016341.4:c.6389T>C (PLCE1) MANE Select	NP_057425.3:p.Leu2130Ser