Canonical Allele Identifier: CA645550158

Gene: PLCE1

Linked Data

• COSMIC: COSM5831613 ; COSM5831614 ; COSM5831615 ; COSM5831616

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298389_94298390insCA , CM000672.2:g.94298389_94298390insCA	GRCh38
NC_000010.10:g.96058146_96058147insCA , CM000672.1:g.96058146_96058147insCA	GRCh37
NC_000010.9:g.96048136_96048137insCA	NCBI36
NG_015799.1:g.309401_309402insCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4254_4255insCA	ENSP00000360426.1:p.Gly1419GlnfsTer?
ENST00000685253.1:c.*1721_*1722insCA	ENSP00000509405.1:n.*1721_*1722insCA
ENST00000685889.1:n.1913_1914insCA
ENST00000686807.1:n.597_598insCA
ENST00000686954.1:c.*462_*463insCA	ENSP00000508416.1:n.*462_*463insCA
ENST00000688810.1:c.4206_4207insCA	ENSP00000509140.1:p.Gly1403GlnfsTer?
ENST00000689233.1:n.9386_9387insCA
ENST00000690340.1:n.2851_2852insCA
ENST00000692286.1:c.5046_5047insCA	ENSP00000509490.1:p.Gly1683GlnfsTer?
ENST00000692396.1:c.5130_5131insCA	ENSP00000508605.1:p.Gly1711GlnfsTer?
ENST00000371380.8:c.5178_5179insCA MANE Select	ENSP00000360431.2:p.Gly1727GlnfsTer?
ENST00000371385.8:c.4152_4153insCA	ENSP00000360438.4:p.Gly1385GlnfsTer?
ENST00000674738.1:c.3733_3734insCA
ENST00000674827.1:c.3294_3295insCA	ENSP00000502523.1:p.Gly1099GlnfsTer?
ENST00000675218.1:c.4254_4255insCA	ENSP00000501910.1:p.Gly1419GlnfsTer?
ENST00000675487.1:c.*1111_*1112insCA	ENSP00000502340.1:n.*1111_*1112insCA
ENST00000675718.1:c.4447_4448insCA
ENST00000676102.1:c.4023_4024insCA	ENSP00000502811.1:p.Gly1342GlnfsTer?
ENST00000260766.7:c.5178_5179insCA	ENSP00000260766.3:p.Gly1727GlnfsTer?
ENST00000371375.1:c.4254_4255insCA	ENSP00000360426.1:p.Gly1419GlnfsTer?
ENST00000371380.7:c.5178_5179insCA	ENSP00000360431.2:p.Gly1727GlnfsTer?
ENST00000371385.7:c.4254_4255insCA	ENSP00000360438.3:p.Gly1419GlnfsTer?
NM_001165979.2:c.4254_4255insCA	NP_001159451.1:p.Gly1419GlnfsTer?
NM_001288989.1:c.5130_5131insCA	NP_001275918.1:p.Gly1711GlnfsTer?
NM_016341.3:c.5178_5179insCA	NP_057425.3:p.Gly1727GlnfsTer?
XM_006717885.2:c.5220_5221insCA	XP_006717948.1:p.Gly1741GlnfsTer?
XM_006717886.2:c.5220_5221insCA	XP_006717949.1:p.Gly1741GlnfsTer?
XM_006717888.2:c.5217_5218insCA	XP_006717951.1:p.Gly1740GlnfsTer?
XM_006717889.2:c.5172_5173insCA	XP_006717952.1:p.Gly1725GlnfsTer?
XM_006717890.1:c.4296_4297insCA	XP_006717953.1:p.Gly1433GlnfsTer?
XM_011539849.1:c.5220_5221insCA	XP_011538151.1:p.Gly1741GlnfsTer?
XM_011539850.1:c.4065_4066insCA	XP_011538152.1:p.Gly1356GlnfsTer?
XM_006717885.4:c.5220_5221insCA	XP_006717948.1:p.Gly1741GlnfsTer?
XM_006717888.4:c.5217_5218insCA	XP_006717951.1:p.Gly1740GlnfsTer?
XM_006717889.4:c.5172_5173insCA	XP_006717952.1:p.Gly1725GlnfsTer?
XM_006717890.3:c.4296_4297insCA	XP_006717953.1:p.Gly1433GlnfsTer?
XM_011539849.3:c.5220_5221insCA	XP_011538151.1:p.Gly1741GlnfsTer?
XM_011539850.3:c.4065_4066insCA	XP_011538152.1:p.Gly1356GlnfsTer?
XM_017016310.2:c.5220_5221insCA	XP_016871799.1:p.Gly1741GlnfsTer?
XM_017016311.2:c.5220_5221insCA	XP_016871800.1:p.Gly1741GlnfsTer?
XM_017016312.2:c.4206_4207insCA	XP_016871801.1:p.Gly1403GlnfsTer?
NM_001288989.2:c.5130_5131insCA	NP_001275918.1:p.Gly1711GlnfsTer?
NM_016341.4:c.5178_5179insCA MANE Select	NP_057425.3:p.Gly1727GlnfsTer?