Canonical Allele Identifier: CA1928996223

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293667G= , CM000672.2:g.94293667G=	GRCh38
NC_000010.10:g.96053424G= , CM000672.1:g.96053424G=	GRCh37
NC_000010.9:g.96043414G=	NCBI36
NG_015799.1:g.304679G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4243+28G=	ENSP00000360426.1:n.4243+28G=
ENST00000685253.1:c.*1710+28G=	ENSP00000509405.1:n.*1710+28G=
ENST00000685889.1:n.1902+28G=
ENST00000686807.1:n.586+28G=
ENST00000686954.1:c.*451+28G=	ENSP00000508416.1:n.*451+28G=
ENST00000688810.1:c.4195+28G=	ENSP00000509140.1:n.4195+28G=
ENST00000689233.1:n.9375+28G=
ENST00000690340.1:n.2840+28G=
ENST00000692286.1:c.5036-4712G=	ENSP00000509490.1:n.5036-4712G=
ENST00000692396.1:c.5119+28G=	ENSP00000508605.1:n.5119+28G=
ENST00000371380.8:c.5167+28G= MANE Select	ENSP00000360431.2:n.5167+28G=
ENST00000371385.8:c.4141+28G=	ENSP00000360438.4:n.4141+28G=
ENST00000674738.1:c.3722+28G=
ENST00000674827.1:c.3283+28G=	ENSP00000502523.1:n.3283+28G=
ENST00000675218.1:c.4243+28G=	ENSP00000501910.1:n.4243+28G=
ENST00000675487.1:c.*1100+28G=	ENSP00000502340.1:n.*1100+28G=
ENST00000675718.1:c.4436+28G=
ENST00000676102.1:c.4012+28G=	ENSP00000502811.1:n.4012+28G=
ENST00000260766.7:c.5167+28G=	ENSP00000260766.3:n.5167+28G=
ENST00000371375.1:c.4243+28G=	ENSP00000360426.1:n.4243+28G=
ENST00000371380.7:c.5167+28G=	ENSP00000360431.2:n.5167+28G=
ENST00000371385.7:c.4243+28G=	ENSP00000360438.3:n.4243+28G=
NM_001165979.2:c.4243+28G=	NP_001159451.1:n.4243+28G=
NM_001288989.1:c.5119+28G=	NP_001275918.1:n.5119+28G=
NM_016341.3:c.5167+28G=	NP_057425.3:n.5167+28G=
XM_006717885.2:c.5209+28G=	XP_006717948.1:n.5209+28G=
XM_006717886.2:c.5209+28G=	XP_006717949.1:n.5209+28G=
XM_006717888.2:c.5206+28G=	XP_006717951.1:n.5206+28G=
XM_006717889.2:c.5161+28G=	XP_006717952.1:n.5161+28G=
XM_006717890.1:c.4285+28G=	XP_006717953.1:n.4285+28G=
XM_011539849.1:c.5209+28G=	XP_011538151.1:n.5209+28G=
XM_011539850.1:c.4054+28G=	XP_011538152.1:n.4054+28G=
XM_006717885.4:c.5209+28G=	XP_006717948.1:n.5209+28G=
XM_006717888.4:c.5206+28G=	XP_006717951.1:n.5206+28G=
XM_006717889.4:c.5161+28G=	XP_006717952.1:n.5161+28G=
XM_006717890.3:c.4285+28G=	XP_006717953.1:n.4285+28G=
XM_011539849.3:c.5209+28G=	XP_011538151.1:n.5209+28G=
XM_011539850.3:c.4054+28G=	XP_011538152.1:n.4054+28G=
XM_017016310.2:c.5209+28G=	XP_016871799.1:n.5209+28G=
XM_017016311.2:c.5209+28G=	XP_016871800.1:n.5209+28G=
XM_017016312.2:c.4195+28G=	XP_016871801.1:n.4195+28G=
NM_001288989.2:c.5119+28G=	NP_001275918.1:n.5119+28G=
NM_016341.4:c.5167+28G= MANE Select	NP_057425.3:n.5167+28G=