Canonical Allele Identifier: CA1928998256

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298094_94298113delinsAGGCTGGTCTTGAACTTCTG , CM000672.2:g.94298094_94298113delinsAGGCTGGTCTTGAACTTCTG	GRCh38
NC_000010.10:g.96057851_96057870delinsAGGCTGGTCTTGAACTTCTG , CM000672.1:g.96057851_96057870delinsAGGCTGGTCTTGAACTTCTG	GRCh37
NC_000010.9:g.96047841_96047860delinsAGGCTGGTCTTGAACTTCTG	NCBI36
NG_015799.1:g.309106_309125delinsAGGCTGGTCTTGAACTTCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4244-285_4244-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000360426.1:n.4244-285_4244-266delinsAGGCTGGTCTTGAACTTC...
ENST00000685253.1:c.*1711-285_*1711-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000509405.1:n.*1711-285_*1711-266delinsAGGCTGGTCTTGAACT...
ENST00000685889.1:n.1903-285_1903-266delinsAGGCTGGTCTTGAACTTCTG
ENST00000686807.1:n.587-285_587-266delinsAGGCTGGTCTTGAACTTCTG
ENST00000686954.1:c.*452-285_*452-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000508416.1:n.*452-285_*452-266delinsAGGCTGGTCTTGAACTTC...
ENST00000688810.1:c.4196-285_4196-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000509140.1:n.4196-285_4196-266delinsAGGCTGGTCTTGAACTTC...
ENST00000689233.1:n.9376-285_9376-266delinsAGGCTGGTCTTGAACTTCTG
ENST00000690340.1:n.2841-285_2841-266delinsAGGCTGGTCTTGAACTTCTG
ENST00000692286.1:c.5036-285_5036-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000509490.1:n.5036-285_5036-266delinsAGGCTGGTCTTGAACTTC...
ENST00000692396.1:c.5120-285_5120-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000508605.1:n.5120-285_5120-266delinsAGGCTGGTCTTGAACTTC...
ENST00000371380.8:c.5168-285_5168-266delinsAGGCTGGTCTTGAACTTCTG MANE Select	ENSP00000360431.2:n.5168-285_5168-266delinsAGGCTGGTCTTGAACTTC...
ENST00000371385.8:c.4142-285_4142-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000360438.4:n.4142-285_4142-266delinsAGGCTGGTCTTGAACTTC...
ENST00000674738.1:c.3723-285_3723-266delinsAGGCTGGTCTTGAACTTCTG
ENST00000674827.1:c.3284-285_3284-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000502523.1:n.3284-285_3284-266delinsAGGCTGGTCTTGAACTTC...
ENST00000675218.1:c.4244-285_4244-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000501910.1:n.4244-285_4244-266delinsAGGCTGGTCTTGAACTTC...
ENST00000675487.1:c.*1101-285_*1101-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000502340.1:n.*1101-285_*1101-266delinsAGGCTGGTCTTGAACT...
ENST00000675718.1:c.4437-285_4437-266delinsAGGCTGGTCTTGAACTTCTG
ENST00000676102.1:c.4013-285_4013-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000502811.1:n.4013-285_4013-266delinsAGGCTGGTCTTGAACTTC...
ENST00000260766.7:c.5168-285_5168-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000260766.3:n.5168-285_5168-266delinsAGGCTGGTCTTGAACTTC...
ENST00000371375.1:c.4244-285_4244-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000360426.1:n.4244-285_4244-266delinsAGGCTGGTCTTGAACTTC...
ENST00000371380.7:c.5168-285_5168-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000360431.2:n.5168-285_5168-266delinsAGGCTGGTCTTGAACTTC...
ENST00000371385.7:c.4244-285_4244-266delinsAGGCTGGTCTTGAACTTCTG	ENSP00000360438.3:n.4244-285_4244-266delinsAGGCTGGTCTTGAACTTC...
NM_001165979.2:c.4244-285_4244-266delinsAGGCTGGTCTTGAACTTCTG	NP_001159451.1:n.4244-285_4244-266delinsAGGCTGGTCTTGAACTTCTG
NM_001288989.1:c.5120-285_5120-266delinsAGGCTGGTCTTGAACTTCTG	NP_001275918.1:n.5120-285_5120-266delinsAGGCTGGTCTTGAACTTCTG
NM_016341.3:c.5168-285_5168-266delinsAGGCTGGTCTTGAACTTCTG	NP_057425.3:n.5168-285_5168-266delinsAGGCTGGTCTTGAACTTCTG
XM_006717885.2:c.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG	XP_006717948.1:n.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG
XM_006717886.2:c.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG	XP_006717949.1:n.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG
XM_006717888.2:c.5207-285_5207-266delinsAGGCTGGTCTTGAACTTCTG	XP_006717951.1:n.5207-285_5207-266delinsAGGCTGGTCTTGAACTTCTG
XM_006717889.2:c.5162-285_5162-266delinsAGGCTGGTCTTGAACTTCTG	XP_006717952.1:n.5162-285_5162-266delinsAGGCTGGTCTTGAACTTCTG
XM_006717890.1:c.4286-285_4286-266delinsAGGCTGGTCTTGAACTTCTG	XP_006717953.1:n.4286-285_4286-266delinsAGGCTGGTCTTGAACTTCTG
XM_011539849.1:c.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG	XP_011538151.1:n.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG
XM_011539850.1:c.4055-285_4055-266delinsAGGCTGGTCTTGAACTTCTG	XP_011538152.1:n.4055-285_4055-266delinsAGGCTGGTCTTGAACTTCTG
XM_006717885.4:c.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG	XP_006717948.1:n.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG
XM_006717888.4:c.5207-285_5207-266delinsAGGCTGGTCTTGAACTTCTG	XP_006717951.1:n.5207-285_5207-266delinsAGGCTGGTCTTGAACTTCTG
XM_006717889.4:c.5162-285_5162-266delinsAGGCTGGTCTTGAACTTCTG	XP_006717952.1:n.5162-285_5162-266delinsAGGCTGGTCTTGAACTTCTG
XM_006717890.3:c.4286-285_4286-266delinsAGGCTGGTCTTGAACTTCTG	XP_006717953.1:n.4286-285_4286-266delinsAGGCTGGTCTTGAACTTCTG
XM_011539849.3:c.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG	XP_011538151.1:n.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG
XM_011539850.3:c.4055-285_4055-266delinsAGGCTGGTCTTGAACTTCTG	XP_011538152.1:n.4055-285_4055-266delinsAGGCTGGTCTTGAACTTCTG
XM_017016310.2:c.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG	XP_016871799.1:n.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG
XM_017016311.2:c.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG	XP_016871800.1:n.5210-285_5210-266delinsAGGCTGGTCTTGAACTTCTG
XM_017016312.2:c.4196-285_4196-266delinsAGGCTGGTCTTGAACTTCTG	XP_016871801.1:n.4196-285_4196-266delinsAGGCTGGTCTTGAACTTCTG
NM_001288989.2:c.5120-285_5120-266delinsAGGCTGGTCTTGAACTTCTG	NP_001275918.1:n.5120-285_5120-266delinsAGGCTGGTCTTGAACTTCTG
NM_016341.4:c.5168-285_5168-266delinsAGGCTGGTCTTGAACTTCTG MANE Select	NP_057425.3:n.5168-285_5168-266delinsAGGCTGGTCTTGAACTTCTG