Canonical Allele Identifier: CA645550160

Gene: PLCE1

Linked Data

• COSMIC: COSM3665975 ; COSM3665976 ; COSM3665977

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298672A>G , CM000672.2:g.94298672A>G	GRCh38
NC_000010.10:g.96058429A>G , CM000672.1:g.96058429A>G	GRCh37
NC_000010.9:g.96048419A>G	NCBI36
NG_015799.1:g.309684A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4534+3A>G	ENSP00000360426.1:n.4534+3A>G
ENST00000685253.1:c.*2001+3A>G	ENSP00000509405.1:n.*2001+3A>G
ENST00000685889.1:n.2193+3A>G
ENST00000686807.1:n.877+3A>G
ENST00000686954.1:c.*742+3A>G	ENSP00000508416.1:n.*742+3A>G
ENST00000688810.1:c.4486+3A>G	ENSP00000509140.1:n.4486+3A>G
ENST00000689233.1:n.9666+3A>G
ENST00000690340.1:n.3131+3A>G
ENST00000692286.1:c.5326+3A>G	ENSP00000509490.1:n.5326+3A>G
ENST00000692396.1:c.5410+3A>G	ENSP00000508605.1:n.5410+3A>G
ENST00000371380.8:c.5458+3A>G MANE Select	ENSP00000360431.2:n.5458+3A>G
ENST00000371385.8:c.4432+3A>G	ENSP00000360438.4:n.4432+3A>G
ENST00000674738.1:c.4013+3A>G
ENST00000674827.1:c.3574+3A>G	ENSP00000502523.1:n.3574+3A>G
ENST00000675218.1:c.4534+3A>G	ENSP00000501910.1:n.4534+3A>G
ENST00000675487.1:c.*1391+3A>G	ENSP00000502340.1:n.*1391+3A>G
ENST00000675718.1:c.4727+3A>G
ENST00000260766.7:c.5458+3A>G	ENSP00000260766.3:n.5458+3A>G
ENST00000371375.1:c.4534+3A>G	ENSP00000360426.1:n.4534+3A>G
ENST00000371380.7:c.5458+3A>G	ENSP00000360431.2:n.5458+3A>G
ENST00000371385.7:c.4534+3A>G	ENSP00000360438.3:n.4534+3A>G
NM_001165979.2:c.4534+3A>G	NP_001159451.1:n.4534+3A>G
NM_001288989.1:c.5410+3A>G	NP_001275918.1:n.5410+3A>G
NM_016341.3:c.5458+3A>G	NP_057425.3:n.5458+3A>G
XM_006717885.2:c.5500+3A>G	XP_006717948.1:n.5500+3A>G
XM_006717886.2:c.5500+3A>G	XP_006717949.1:n.5500+3A>G
XM_006717888.2:c.5497+3A>G	XP_006717951.1:n.5497+3A>G
XM_006717889.2:c.5452+3A>G	XP_006717952.1:n.5452+3A>G
XM_006717890.1:c.4576+3A>G	XP_006717953.1:n.4576+3A>G
XM_011539849.1:c.5500+3A>G	XP_011538151.1:n.5500+3A>G
XM_011539850.1:c.4345+3A>G	XP_011538152.1:n.4345+3A>G
XM_006717885.4:c.5500+3A>G	XP_006717948.1:n.5500+3A>G
XM_006717888.4:c.5497+3A>G	XP_006717951.1:n.5497+3A>G
XM_006717889.4:c.5452+3A>G	XP_006717952.1:n.5452+3A>G
XM_006717890.3:c.4576+3A>G	XP_006717953.1:n.4576+3A>G
XM_011539849.3:c.5500+3A>G	XP_011538151.1:n.5500+3A>G
XM_011539850.3:c.4345+3A>G	XP_011538152.1:n.4345+3A>G
XM_017016310.2:c.5500+3A>G	XP_016871799.1:n.5500+3A>G
XM_017016311.2:c.5500+3A>G	XP_016871800.1:n.5500+3A>G
XM_017016312.2:c.4486+3A>G	XP_016871801.1:n.4486+3A>G
NM_001288989.2:c.5410+3A>G	NP_001275918.1:n.5410+3A>G
NM_016341.4:c.5458+3A>G MANE Select	NP_057425.3:n.5458+3A>G