Canonical Allele Identifier: CA645550159

Gene: PLCE1

Linked Data

• COSMIC: COSM5831618 ; COSM5831619 ; COSM5831620 ; COSM5831621

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298535_94298536insT , CM000672.2:g.94298535_94298536insT	GRCh38
NC_000010.10:g.96058292_96058293insT , CM000672.1:g.96058292_96058293insT	GRCh37
NC_000010.9:g.96048282_96048283insT	NCBI36
NG_015799.1:g.309547_309548insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4400_4401insT	ENSP00000360426.1:p.Lys1467AsnfsTer?
ENST00000685253.1:c.*1867_*1868insT	ENSP00000509405.1:n.*1867_*1868insT
ENST00000685889.1:n.2059_2060insT
ENST00000686807.1:n.743_744insT
ENST00000686954.1:c.*608_*609insT	ENSP00000508416.1:n.*608_*609insT
ENST00000688810.1:c.4352_4353insT	ENSP00000509140.1:p.Lys1451AsnfsTer?
ENST00000689233.1:n.9532_9533insT
ENST00000690340.1:n.2997_2998insT
ENST00000692286.1:c.5192_5193insT	ENSP00000509490.1:p.Lys1731AsnfsTer?
ENST00000692396.1:c.5276_5277insT	ENSP00000508605.1:p.Lys1759AsnfsTer?
ENST00000371380.8:c.5324_5325insT MANE Select	ENSP00000360431.2:p.Lys1775AsnfsTer?
ENST00000371385.8:c.4298_4299insT	ENSP00000360438.4:p.Lys1433AsnfsTer?
ENST00000674738.1:c.3879_3880insT
ENST00000674827.1:c.3440_3441insT	ENSP00000502523.1:p.Lys1147AsnfsTer?
ENST00000675218.1:c.4400_4401insT	ENSP00000501910.1:p.Lys1467AsnfsTer?
ENST00000675487.1:c.*1257_*1258insT	ENSP00000502340.1:n.*1257_*1258insT
ENST00000675718.1:c.4593_4594insT
ENST00000260766.7:c.5324_5325insT	ENSP00000260766.3:p.Lys1775AsnfsTer?
ENST00000371375.1:c.4400_4401insT	ENSP00000360426.1:p.Lys1467AsnfsTer?
ENST00000371380.7:c.5324_5325insT	ENSP00000360431.2:p.Lys1775AsnfsTer?
ENST00000371385.7:c.4400_4401insT	ENSP00000360438.3:p.Lys1467AsnfsTer?
NM_001165979.2:c.4400_4401insT	NP_001159451.1:p.Lys1467AsnfsTer?
NM_001288989.1:c.5276_5277insT	NP_001275918.1:p.Lys1759AsnfsTer?
NM_016341.3:c.5324_5325insT	NP_057425.3:p.Lys1775AsnfsTer?
XM_006717885.2:c.5366_5367insT	XP_006717948.1:p.Lys1789AsnfsTer?
XM_006717886.2:c.5366_5367insT	XP_006717949.1:p.Lys1789AsnfsTer?
XM_006717888.2:c.5363_5364insT	XP_006717951.1:p.Lys1788AsnfsTer?
XM_006717889.2:c.5318_5319insT	XP_006717952.1:p.Lys1773AsnfsTer?
XM_006717890.1:c.4442_4443insT	XP_006717953.1:p.Lys1481AsnfsTer?
XM_011539849.1:c.5366_5367insT	XP_011538151.1:p.Lys1789AsnfsTer?
XM_011539850.1:c.4211_4212insT	XP_011538152.1:p.Lys1404AsnfsTer?
XM_006717885.4:c.5366_5367insT	XP_006717948.1:p.Lys1789AsnfsTer?
XM_006717888.4:c.5363_5364insT	XP_006717951.1:p.Lys1788AsnfsTer?
XM_006717889.4:c.5318_5319insT	XP_006717952.1:p.Lys1773AsnfsTer?
XM_006717890.3:c.4442_4443insT	XP_006717953.1:p.Lys1481AsnfsTer?
XM_011539849.3:c.5366_5367insT	XP_011538151.1:p.Lys1789AsnfsTer?
XM_011539850.3:c.4211_4212insT	XP_011538152.1:p.Lys1404AsnfsTer?
XM_017016310.2:c.5366_5367insT	XP_016871799.1:p.Lys1789AsnfsTer?
XM_017016311.2:c.5366_5367insT	XP_016871800.1:p.Lys1789AsnfsTer?
XM_017016312.2:c.4352_4353insT	XP_016871801.1:p.Lys1451AsnfsTer?
NM_001288989.2:c.5276_5277insT	NP_001275918.1:p.Lys1759AsnfsTer?
NM_016341.4:c.5324_5325insT MANE Select	NP_057425.3:p.Lys1775AsnfsTer?