Canonical Allele Identifier: CA2574455539

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293732_94293735del , CM000672.2:g.94293732_94293735del	GRCh38
NC_000010.10:g.96053489_96053492del , CM000672.1:g.96053489_96053492del	GRCh37
NC_000010.9:g.96043479_96043482del	NCBI36
NG_015799.1:g.304744_304747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4243+93_4243+96del	ENSP00000360426.1:n.4243+93_4243+96del
ENST00000685253.1:c.*1710+93_*1710+96del	ENSP00000509405.1:n.*1710+93_*1710+96del
ENST00000685889.1:n.1902+93_1902+96del
ENST00000686807.1:n.586+93_586+96del
ENST00000686954.1:c.*451+93_*451+96del	ENSP00000508416.1:n.*451+93_*451+96del
ENST00000688810.1:c.4195+93_4195+96del	ENSP00000509140.1:n.4195+93_4195+96del
ENST00000689233.1:n.9375+93_9375+96del
ENST00000690340.1:n.2840+93_2840+96del
ENST00000692286.1:c.5036-4647_5036-4644del	ENSP00000509490.1:n.5036-4647_5036-4644del
ENST00000692396.1:c.5119+93_5119+96del	ENSP00000508605.1:n.5119+93_5119+96del
ENST00000371380.8:c.5167+93_5167+96del MANE Select	ENSP00000360431.2:n.5167+93_5167+96del
ENST00000371385.8:c.4141+93_4141+96del	ENSP00000360438.4:n.4141+93_4141+96del
ENST00000674738.1:c.3722+93_3722+96del
ENST00000674827.1:c.3283+93_3283+96del	ENSP00000502523.1:n.3283+93_3283+96del
ENST00000675218.1:c.4243+93_4243+96del	ENSP00000501910.1:n.4243+93_4243+96del
ENST00000675487.1:c.*1100+93_*1100+96del	ENSP00000502340.1:n.*1100+93_*1100+96del
ENST00000675718.1:c.4436+93_4436+96del
ENST00000676102.1:c.4012+93_4012+96del	ENSP00000502811.1:n.4012+93_4012+96del
ENST00000260766.7:c.5167+93_5167+96del	ENSP00000260766.3:n.5167+93_5167+96del
ENST00000371375.1:c.4243+93_4243+96del	ENSP00000360426.1:n.4243+93_4243+96del
ENST00000371380.7:c.5167+93_5167+96del	ENSP00000360431.2:n.5167+93_5167+96del
ENST00000371385.7:c.4243+93_4243+96del	ENSP00000360438.3:n.4243+93_4243+96del
NM_001165979.2:c.4243+93_4243+96del	NP_001159451.1:n.4243+93_4243+96del
NM_001288989.1:c.5119+93_5119+96del	NP_001275918.1:n.5119+93_5119+96del
NM_016341.3:c.5167+93_5167+96del	NP_057425.3:n.5167+93_5167+96del
XM_006717885.2:c.5209+93_5209+96del	XP_006717948.1:n.5209+93_5209+96del
XM_006717886.2:c.5209+93_5209+96del	XP_006717949.1:n.5209+93_5209+96del
XM_006717888.2:c.5206+93_5206+96del	XP_006717951.1:n.5206+93_5206+96del
XM_006717889.2:c.5161+93_5161+96del	XP_006717952.1:n.5161+93_5161+96del
XM_006717890.1:c.4285+93_4285+96del	XP_006717953.1:n.4285+93_4285+96del
XM_011539849.1:c.5209+93_5209+96del	XP_011538151.1:n.5209+93_5209+96del
XM_011539850.1:c.4054+93_4054+96del	XP_011538152.1:n.4054+93_4054+96del
XM_006717885.4:c.5209+93_5209+96del	XP_006717948.1:n.5209+93_5209+96del
XM_006717888.4:c.5206+93_5206+96del	XP_006717951.1:n.5206+93_5206+96del
XM_006717889.4:c.5161+93_5161+96del	XP_006717952.1:n.5161+93_5161+96del
XM_006717890.3:c.4285+93_4285+96del	XP_006717953.1:n.4285+93_4285+96del
XM_011539849.3:c.5209+93_5209+96del	XP_011538151.1:n.5209+93_5209+96del
XM_011539850.3:c.4054+93_4054+96del	XP_011538152.1:n.4054+93_4054+96del
XM_017016310.2:c.5209+93_5209+96del	XP_016871799.1:n.5209+93_5209+96del
XM_017016311.2:c.5209+93_5209+96del	XP_016871800.1:n.5209+93_5209+96del
XM_017016312.2:c.4195+93_4195+96del	XP_016871801.1:n.4195+93_4195+96del
NM_001288989.2:c.5119+93_5119+96del	NP_001275918.1:n.5119+93_5119+96del
NM_016341.4:c.5167+93_5167+96del MANE Select	NP_057425.3:n.5167+93_5167+96del