Canonical Allele Identifier: CA377648120

Gene: PLCE1 NOC3L

Linked Data

• MyVariant Identifiers: chr10:g.96081671A>G (hg19) ; chr10:g.94321914A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94321914A>G , CM000672.2:g.94321914A>G	GRCh38
NC_000010.10:g.96081671A>G , CM000672.1:g.96081671A>G	GRCh37
NC_000010.9:g.96071661A>G	NCBI36
NG_015799.1:g.332926A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.5432A>G (PLCE1)	ENSP00000360426.1:p.Lys1811Arg
ENST00000685132.1:n.3755A>G (PLCE1)
ENST00000685253.1:c.*2899A>G (PLCE1)	ENSP00000509405.1:n.*2899A>G
ENST00000685889.1:n.3091A>G (PLCE1)
ENST00000686807.1:n.1775A>G (PLCE1)
ENST00000686954.1:c.*1640A>G (PLCE1)	ENSP00000508416.1:n.*1640A>G
ENST00000688810.1:c.5384A>G (PLCE1)	ENSP00000509140.1:p.Lys1795Arg
ENST00000689233.1:n.10564A>G (PLCE1)
ENST00000690340.1:n.4029A>G (PLCE1)
ENST00000692286.1:c.6224A>G (PLCE1)	ENSP00000509490.1:p.Lys2075Arg
ENST00000692396.1:c.6308A>G (PLCE1)	ENSP00000508605.1:p.Lys2103Arg
ENST00000371380.8:c.6356A>G (PLCE1) MANE Select	ENSP00000360431.2:p.Lys2119Arg
ENST00000371385.8:c.5330A>G (PLCE1)	ENSP00000360438.4:p.Lys1777Arg
ENST00000674738.1:c.4911A>G (PLCE1)
ENST00000674827.1:c.4472A>G (PLCE1)	ENSP00000502523.1:p.Lys1491Arg
ENST00000675218.1:c.5432A>G (PLCE1)	ENSP00000501910.1:p.Lys1811Arg
ENST00000675487.1:c.*2289A>G (PLCE1)	ENSP00000502340.1:n.*2289A>G
ENST00000675718.1:c.5625A>G (PLCE1)
ENST00000260766.7:c.6356A>G (PLCE1)	ENSP00000260766.3:p.Lys2119Arg
ENST00000371375.1:c.5432A>G (PLCE1)	ENSP00000360426.1:p.Lys1811Arg
ENST00000371380.7:c.6356A>G (PLCE1)	ENSP00000360431.2:p.Lys2119Arg
ENST00000371385.7:c.5432A>G (PLCE1)	ENSP00000360438.3:p.Lys1811Arg
NM_001165979.2:c.5432A>G (PLCE1)	NP_001159451.1:p.Lys1811Arg
NM_001288989.1:c.6308A>G (PLCE1)	NP_001275918.1:p.Lys2103Arg
NM_016341.3:c.6356A>G (PLCE1)	NP_057425.3:p.Lys2119Arg
XM_006717885.2:c.6398A>G (PLCE1)	XP_006717948.1:p.Lys2133Arg
XM_006717886.2:c.6398A>G (PLCE1)	XP_006717949.1:p.Lys2133Arg
XM_006717888.2:c.6395A>G (PLCE1)	XP_006717951.1:p.Lys2132Arg
XM_006717889.2:c.6350A>G (PLCE1)	XP_006717952.1:p.Lys2117Arg
XM_006717890.1:c.5474A>G (PLCE1)	XP_006717953.1:p.Lys1825Arg
XM_011539849.1:c.6398A>G (PLCE1)	XP_011538151.1:p.Lys2133Arg
XM_011539850.1:c.5243A>G (PLCE1)	XP_011538152.1:p.Lys1748Arg
XR_945799.1:n.3311-6450T>C (NOC3L)
XM_006717885.4:c.6398A>G (PLCE1)	XP_006717948.1:p.Lys2133Arg
XM_006717888.4:c.6395A>G (PLCE1)	XP_006717951.1:p.Lys2132Arg
XM_006717889.4:c.6350A>G (PLCE1)	XP_006717952.1:p.Lys2117Arg
XM_006717890.3:c.5474A>G (PLCE1)	XP_006717953.1:p.Lys1825Arg
XM_011539849.3:c.6398A>G (PLCE1)	XP_011538151.1:p.Lys2133Arg
XM_011539850.3:c.5243A>G (PLCE1)	XP_011538152.1:p.Lys1748Arg
XM_017016310.2:c.6398A>G (PLCE1)	XP_016871799.1:p.Lys2133Arg
XM_017016311.2:c.6398A>G (PLCE1)	XP_016871800.1:p.Lys2133Arg
XM_017016312.2:c.5384A>G (PLCE1)	XP_016871801.1:p.Lys1795Arg
XR_002957007.1:n.3312-6450T>C (NOC3L)
NM_001288989.2:c.6308A>G (PLCE1)	NP_001275918.1:p.Lys2103Arg
NM_016341.4:c.6356A>G (PLCE1) MANE Select	NP_057425.3:p.Lys2119Arg