Canonical Allele Identifier: CA2610239584

Gene: PLCE1

Linked Data

• gnomAD v4: 10-94298242-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298245_94298246del , CM000672.2:g.94298245_94298246del	GRCh38
NC_000010.10:g.96058002_96058003del , CM000672.1:g.96058002_96058003del	GRCh37
NC_000010.9:g.96047992_96047993del	NCBI36
NG_015799.1:g.309257_309258del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4244-134_4244-133del	ENSP00000360426.1:n.4244-134_4244-133del
ENST00000685253.1:c.*1711-134_*1711-133del	ENSP00000509405.1:n.*1711-134_*1711-133de...
ENST00000685889.1:n.1903-134_1903-133del
ENST00000686807.1:n.587-134_587-133del
ENST00000686954.1:c.*452-134_*452-133del	ENSP00000508416.1:n.*452-134_*452-133del
ENST00000688810.1:c.4196-134_4196-133del	ENSP00000509140.1:n.4196-134_4196-133del
ENST00000689233.1:n.9376-134_9376-133del
ENST00000690340.1:n.2841-134_2841-133del
ENST00000692286.1:c.5036-134_5036-133del	ENSP00000509490.1:n.5036-134_5036-133del
ENST00000692396.1:c.5120-134_5120-133del	ENSP00000508605.1:n.5120-134_5120-133del
ENST00000371380.8:c.5168-134_5168-133del MANE Select	ENSP00000360431.2:n.5168-134_5168-133del
ENST00000371385.8:c.4142-134_4142-133del	ENSP00000360438.4:n.4142-134_4142-133del
ENST00000674738.1:c.3723-134_3723-133del
ENST00000674827.1:c.3284-134_3284-133del	ENSP00000502523.1:n.3284-134_3284-133del
ENST00000675218.1:c.4244-134_4244-133del	ENSP00000501910.1:n.4244-134_4244-133del
ENST00000675487.1:c.*1101-134_*1101-133del	ENSP00000502340.1:n.*1101-134_*1101-133de...
ENST00000675718.1:c.4437-134_4437-133del
ENST00000676102.1:c.4013-134_4013-133del	ENSP00000502811.1:n.4013-134_4013-133del
ENST00000260766.7:c.5168-134_5168-133del	ENSP00000260766.3:n.5168-134_5168-133del
ENST00000371375.1:c.4244-134_4244-133del	ENSP00000360426.1:n.4244-134_4244-133del
ENST00000371380.7:c.5168-134_5168-133del	ENSP00000360431.2:n.5168-134_5168-133del
ENST00000371385.7:c.4244-134_4244-133del	ENSP00000360438.3:n.4244-134_4244-133del
NM_001165979.2:c.4244-134_4244-133del	NP_001159451.1:n.4244-134_4244-133del
NM_001288989.1:c.5120-134_5120-133del	NP_001275918.1:n.5120-134_5120-133del
NM_016341.3:c.5168-134_5168-133del	NP_057425.3:n.5168-134_5168-133del
XM_006717885.2:c.5210-134_5210-133del	XP_006717948.1:n.5210-134_5210-133del
XM_006717886.2:c.5210-134_5210-133del	XP_006717949.1:n.5210-134_5210-133del
XM_006717888.2:c.5207-134_5207-133del	XP_006717951.1:n.5207-134_5207-133del
XM_006717889.2:c.5162-134_5162-133del	XP_006717952.1:n.5162-134_5162-133del
XM_006717890.1:c.4286-134_4286-133del	XP_006717953.1:n.4286-134_4286-133del
XM_011539849.1:c.5210-134_5210-133del	XP_011538151.1:n.5210-134_5210-133del
XM_011539850.1:c.4055-134_4055-133del	XP_011538152.1:n.4055-134_4055-133del
XM_006717885.4:c.5210-134_5210-133del	XP_006717948.1:n.5210-134_5210-133del
XM_006717888.4:c.5207-134_5207-133del	XP_006717951.1:n.5207-134_5207-133del
XM_006717889.4:c.5162-134_5162-133del	XP_006717952.1:n.5162-134_5162-133del
XM_006717890.3:c.4286-134_4286-133del	XP_006717953.1:n.4286-134_4286-133del
XM_011539849.3:c.5210-134_5210-133del	XP_011538151.1:n.5210-134_5210-133del
XM_011539850.3:c.4055-134_4055-133del	XP_011538152.1:n.4055-134_4055-133del
XM_017016310.2:c.5210-134_5210-133del	XP_016871799.1:n.5210-134_5210-133del
XM_017016311.2:c.5210-134_5210-133del	XP_016871800.1:n.5210-134_5210-133del
XM_017016312.2:c.4196-134_4196-133del	XP_016871801.1:n.4196-134_4196-133del
NM_001288989.2:c.5120-134_5120-133del	NP_001275918.1:n.5120-134_5120-133del
NM_016341.4:c.5168-134_5168-133del MANE Select	NP_057425.3:n.5168-134_5168-133del