Canonical Allele Identifier: CA1929017112

Gene: PLCE1 NOC3L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94322060G= , CM000672.2:g.94322060G=	GRCh38
NC_000010.10:g.96081817G= , CM000672.1:g.96081817G=	GRCh37
NC_000010.9:g.96071807G=	NCBI36
NG_015799.1:g.333072G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.5577+1G= (PLCE1)	ENSP00000360426.1:n.5577+1G=
ENST00000685253.1:c.*3044+1G= (PLCE1)	ENSP00000509405.1:n.*3044+1G=
ENST00000685889.1:n.3236+1G= (PLCE1)
ENST00000686807.1:n.1920+1G= (PLCE1)
ENST00000686954.1:c.*1785+1G= (PLCE1)	ENSP00000508416.1:n.*1785+1G=
ENST00000688810.1:c.5529+1G= (PLCE1)	ENSP00000509140.1:n.5529+1G=
ENST00000689233.1:n.10709+1G= (PLCE1)
ENST00000690340.1:n.4174+1G= (PLCE1)
ENST00000692286.1:c.6369+1G= (PLCE1)	ENSP00000509490.1:n.6369+1G=
ENST00000692396.1:c.6453+1G= (PLCE1)	ENSP00000508605.1:n.6453+1G=
ENST00000371380.8:c.6501+1G= (PLCE1) MANE Select	ENSP00000360431.2:n.6501+1G=
ENST00000371385.8:c.5475+1G= (PLCE1)	ENSP00000360438.4:n.5475+1G=
ENST00000675218.1:c.5577+1G= (PLCE1)	ENSP00000501910.1:n.5577+1G=
ENST00000675487.1:c.*2434+1G= (PLCE1)	ENSP00000502340.1:n.*2434+1G=
ENST00000260766.7:c.6501+1G= (PLCE1)	ENSP00000260766.3:n.6501+1G=
ENST00000371375.1:c.5577+1G= (PLCE1)	ENSP00000360426.1:n.5577+1G=
ENST00000371380.7:c.6501+1G= (PLCE1)	ENSP00000360431.2:n.6501+1G=
ENST00000371385.7:c.5577+1G= (PLCE1)	ENSP00000360438.3:n.5577+1G=
NM_001165979.2:c.5577+1G= (PLCE1)	NP_001159451.1:n.5577+1G=
NM_001288989.1:c.6453+1G= (PLCE1)	NP_001275918.1:n.6453+1G=
NM_016341.3:c.6501+1G= (PLCE1)	NP_057425.3:n.6501+1G=
XM_006717885.2:c.6543+1G= (PLCE1)	XP_006717948.1:n.6543+1G=
XM_006717886.2:c.6543+1G= (PLCE1)	XP_006717949.1:n.6543+1G=
XM_006717888.2:c.6540+1G= (PLCE1)	XP_006717951.1:n.6540+1G=
XM_006717889.2:c.6495+1G= (PLCE1)	XP_006717952.1:n.6495+1G=
XM_006717890.1:c.5619+1G= (PLCE1)	XP_006717953.1:n.5619+1G=
XM_011539849.1:c.6543+1G= (PLCE1)	XP_011538151.1:n.6543+1G=
XM_011539850.1:c.5388+1G= (PLCE1)	XP_011538152.1:n.5388+1G=
XR_945799.1:n.3311-6596C= (NOC3L)
XM_006717885.4:c.6543+1G= (PLCE1)	XP_006717948.1:n.6543+1G=
XM_006717888.4:c.6540+1G= (PLCE1)	XP_006717951.1:n.6540+1G=
XM_006717889.4:c.6495+1G= (PLCE1)	XP_006717952.1:n.6495+1G=
XM_006717890.3:c.5619+1G= (PLCE1)	XP_006717953.1:n.5619+1G=
XM_011539849.3:c.6543+1G= (PLCE1)	XP_011538151.1:n.6543+1G=
XM_011539850.3:c.5388+1G= (PLCE1)	XP_011538152.1:n.5388+1G=
XM_017016310.2:c.6543+1G= (PLCE1)	XP_016871799.1:n.6543+1G=
XM_017016311.2:c.6543+1G= (PLCE1)	XP_016871800.1:n.6543+1G=
XM_017016312.2:c.5529+1G= (PLCE1)	XP_016871801.1:n.5529+1G=
XR_002957007.1:n.3312-6596C= (NOC3L)
NM_001288989.2:c.6453+1G= (PLCE1)	NP_001275918.1:n.6453+1G=
NM_016341.4:c.6501+1G= (PLCE1) MANE Select	NP_057425.3:n.6501+1G=