Canonical Allele Identifier: CA670127795

Gene: PLCE1

Linked Data

• dbSNP Id: rs1268254044
• gnomAD v3: 10-94298007-TTTG-T
• gnomAD v4: 10-94298007-TTTG-T
• MyVariant Identifiers: chr10:g.96057765_96057767del (hg19) ; chr10:g.94298008_94298010del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298010_94298012del , CM000672.2:g.94298010_94298012del	GRCh38
NC_000010.10:g.96057767_96057769del , CM000672.1:g.96057767_96057769del	GRCh37
NC_000010.9:g.96047757_96047759del	NCBI36
NG_015799.1:g.309022_309024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4244-369_4244-367del	ENSP00000360426.1:n.4244-369_4244-367del
ENST00000685253.1:c.*1711-369_*1711-367del	ENSP00000509405.1:n.*1711-369_*1711-367del
ENST00000685889.1:n.1903-369_1903-367del
ENST00000686807.1:n.587-369_587-367del
ENST00000686954.1:c.*452-369_*452-367del	ENSP00000508416.1:n.*452-369_*452-367del
ENST00000688810.1:c.4196-369_4196-367del	ENSP00000509140.1:n.4196-369_4196-367del
ENST00000689233.1:n.9376-369_9376-367del
ENST00000690340.1:n.2841-369_2841-367del
ENST00000692286.1:c.5036-369_5036-367del	ENSP00000509490.1:n.5036-369_5036-367del
ENST00000692396.1:c.5120-369_5120-367del	ENSP00000508605.1:n.5120-369_5120-367del
ENST00000371380.8:c.5168-369_5168-367del MANE Select	ENSP00000360431.2:n.5168-369_5168-367del
ENST00000371385.8:c.4142-369_4142-367del	ENSP00000360438.4:n.4142-369_4142-367del
ENST00000674738.1:c.3723-369_3723-367del
ENST00000674827.1:c.3284-369_3284-367del	ENSP00000502523.1:n.3284-369_3284-367del
ENST00000675218.1:c.4244-369_4244-367del	ENSP00000501910.1:n.4244-369_4244-367del
ENST00000675487.1:c.*1101-369_*1101-367del	ENSP00000502340.1:n.*1101-369_*1101-367del
ENST00000675718.1:c.4437-369_4437-367del
ENST00000676102.1:c.4013-369_4013-367del	ENSP00000502811.1:n.4013-369_4013-367del
ENST00000260766.7:c.5168-369_5168-367del	ENSP00000260766.3:n.5168-369_5168-367del
ENST00000371375.1:c.4244-369_4244-367del	ENSP00000360426.1:n.4244-369_4244-367del
ENST00000371380.7:c.5168-369_5168-367del	ENSP00000360431.2:n.5168-369_5168-367del
ENST00000371385.7:c.4244-369_4244-367del	ENSP00000360438.3:n.4244-369_4244-367del
NM_001165979.2:c.4244-369_4244-367del	NP_001159451.1:n.4244-369_4244-367del
NM_001288989.1:c.5120-369_5120-367del	NP_001275918.1:n.5120-369_5120-367del
NM_016341.3:c.5168-369_5168-367del	NP_057425.3:n.5168-369_5168-367del
XM_006717885.2:c.5210-369_5210-367del	XP_006717948.1:n.5210-369_5210-367del
XM_006717886.2:c.5210-369_5210-367del	XP_006717949.1:n.5210-369_5210-367del
XM_006717888.2:c.5207-369_5207-367del	XP_006717951.1:n.5207-369_5207-367del
XM_006717889.2:c.5162-369_5162-367del	XP_006717952.1:n.5162-369_5162-367del
XM_006717890.1:c.4286-369_4286-367del	XP_006717953.1:n.4286-369_4286-367del
XM_011539849.1:c.5210-369_5210-367del	XP_011538151.1:n.5210-369_5210-367del
XM_011539850.1:c.4055-369_4055-367del	XP_011538152.1:n.4055-369_4055-367del
XM_006717885.4:c.5210-369_5210-367del	XP_006717948.1:n.5210-369_5210-367del
XM_006717888.4:c.5207-369_5207-367del	XP_006717951.1:n.5207-369_5207-367del
XM_006717889.4:c.5162-369_5162-367del	XP_006717952.1:n.5162-369_5162-367del
XM_006717890.3:c.4286-369_4286-367del	XP_006717953.1:n.4286-369_4286-367del
XM_011539849.3:c.5210-369_5210-367del	XP_011538151.1:n.5210-369_5210-367del
XM_011539850.3:c.4055-369_4055-367del	XP_011538152.1:n.4055-369_4055-367del
XM_017016310.2:c.5210-369_5210-367del	XP_016871799.1:n.5210-369_5210-367del
XM_017016311.2:c.5210-369_5210-367del	XP_016871800.1:n.5210-369_5210-367del
XM_017016312.2:c.4196-369_4196-367del	XP_016871801.1:n.4196-369_4196-367del
NM_001288989.2:c.5120-369_5120-367del	NP_001275918.1:n.5120-369_5120-367del
NM_016341.4:c.5168-369_5168-367del MANE Select	NP_057425.3:n.5168-369_5168-367del