Canonical Allele Identifier: CA470812279

Gene: PLCE1 NOC3L

Linked Data

• MyVariant Identifiers: chr10:g.96081732C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94321975C>A , CM000672.2:g.94321975C>A	GRCh38
NC_000010.10:g.96081732C>A , CM000672.1:g.96081732C>A	GRCh37
NC_000010.9:g.96071722C>A	NCBI36
NG_015799.1:g.332987C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.5493C>A (PLCE1)	ENSP00000360426.1:p.Val1831=
ENST00000685132.1:n.3816C>A (PLCE1)
ENST00000685253.1:c.*2960C>A (PLCE1)	ENSP00000509405.1:n.*2960C>A
ENST00000685889.1:n.3152C>A (PLCE1)
ENST00000686807.1:n.1836C>A (PLCE1)
ENST00000686954.1:c.*1701C>A (PLCE1)	ENSP00000508416.1:n.*1701C>A
ENST00000688810.1:c.5445C>A (PLCE1)	ENSP00000509140.1:p.Val1815=
ENST00000689233.1:n.10625C>A (PLCE1)
ENST00000690340.1:n.4090C>A (PLCE1)
ENST00000692286.1:c.6285C>A (PLCE1)	ENSP00000509490.1:p.Val2095=
ENST00000692396.1:c.6369C>A (PLCE1)	ENSP00000508605.1:p.Val2123=
ENST00000371380.8:c.6417C>A (PLCE1) MANE Select	ENSP00000360431.2:p.Val2139=
ENST00000371385.8:c.5391C>A (PLCE1)	ENSP00000360438.4:p.Val1797=
ENST00000674738.1:c.4972C>A (PLCE1)
ENST00000674827.1:c.4533C>A (PLCE1)	ENSP00000502523.1:p.Val1511=
ENST00000675218.1:c.5493C>A (PLCE1)	ENSP00000501910.1:p.Val1831=
ENST00000675487.1:c.*2350C>A (PLCE1)	ENSP00000502340.1:n.*2350C>A
ENST00000675718.1:c.5686C>A (PLCE1)
ENST00000260766.7:c.6417C>A (PLCE1)	ENSP00000260766.3:p.Val2139=
ENST00000371375.1:c.5493C>A (PLCE1)	ENSP00000360426.1:p.Val1831=
ENST00000371380.7:c.6417C>A (PLCE1)	ENSP00000360431.2:p.Val2139=
ENST00000371385.7:c.5493C>A (PLCE1)	ENSP00000360438.3:p.Val1831=
NM_001165979.2:c.5493C>A (PLCE1)	NP_001159451.1:p.Val1831=
NM_001288989.1:c.6369C>A (PLCE1)	NP_001275918.1:p.Val2123=
NM_016341.3:c.6417C>A (PLCE1)	NP_057425.3:p.Val2139=
XM_006717885.2:c.6459C>A (PLCE1)	XP_006717948.1:p.Val2153=
XM_006717886.2:c.6459C>A (PLCE1)	XP_006717949.1:p.Val2153=
XM_006717888.2:c.6456C>A (PLCE1)	XP_006717951.1:p.Val2152=
XM_006717889.2:c.6411C>A (PLCE1)	XP_006717952.1:p.Val2137=
XM_006717890.1:c.5535C>A (PLCE1)	XP_006717953.1:p.Val1845=
XM_011539849.1:c.6459C>A (PLCE1)	XP_011538151.1:p.Val2153=
XM_011539850.1:c.5304C>A (PLCE1)	XP_011538152.1:p.Val1768=
XR_945799.1:n.3311-6511G>T (NOC3L)
XM_006717885.4:c.6459C>A (PLCE1)	XP_006717948.1:p.Val2153=
XM_006717888.4:c.6456C>A (PLCE1)	XP_006717951.1:p.Val2152=
XM_006717889.4:c.6411C>A (PLCE1)	XP_006717952.1:p.Val2137=
XM_006717890.3:c.5535C>A (PLCE1)	XP_006717953.1:p.Val1845=
XM_011539849.3:c.6459C>A (PLCE1)	XP_011538151.1:p.Val2153=
XM_011539850.3:c.5304C>A (PLCE1)	XP_011538152.1:p.Val1768=
XM_017016310.2:c.6459C>A (PLCE1)	XP_016871799.1:p.Val2153=
XM_017016311.2:c.6459C>A (PLCE1)	XP_016871800.1:p.Val2153=
XM_017016312.2:c.5445C>A (PLCE1)	XP_016871801.1:p.Val1815=
XR_002957007.1:n.3312-6511G>T (NOC3L)
NM_001288989.2:c.6369C>A (PLCE1)	NP_001275918.1:p.Val2123=
NM_016341.4:c.6417C>A (PLCE1) MANE Select	NP_057425.3:p.Val2139=