Canonical Allele Identifier: CA377651597

Gene: PLCE1 PLCE1-AS1

Linked Data

• MyVariant Identifiers: chr10:g.96039578G>C (hg19) ; chr10:g.94279821G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94279821G>C , CM000672.2:g.94279821G>C	GRCh38
NC_000010.10:g.96039578G>C , CM000672.1:g.96039578G>C	GRCh37
NC_000010.9:g.96029568G>C	NCBI36
NG_015799.1:g.290833G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.3781G>C (PLCE1)	ENSP00000360426.1:p.Gly1261Arg
ENST00000685253.1:c.*1248G>C (PLCE1)	ENSP00000509405.1:n.*1248G>C
ENST00000685889.1:n.1440G>C (PLCE1)
ENST00000686954.1:c.4705G>C (PLCE1)	ENSP00000508416.1:p.Gly1569Arg
ENST00000688810.1:c.3733G>C (PLCE1)	ENSP00000509140.1:p.Gly1245Arg
ENST00000689233.1:n.5035G>C (PLCE1)
ENST00000692286.1:c.4705G>C (PLCE1)	ENSP00000509490.1:p.Gly1569Arg
ENST00000692396.1:c.4657G>C (PLCE1)	ENSP00000508605.1:p.Gly1553Arg
ENST00000371380.8:c.4705G>C (PLCE1) MANE Select	ENSP00000360431.2:p.Gly1569Arg
ENST00000371385.8:c.3679G>C (PLCE1)	ENSP00000360438.4:p.Gly1227Arg
ENST00000674738.1:c.3110G>C (PLCE1)
ENST00000674827.1:c.2782G>C (PLCE1)	ENSP00000502523.1:p.Gly928Arg
ENST00000675218.1:c.3781G>C (PLCE1)	ENSP00000501910.1:p.Gly1261Arg
ENST00000675487.1:c.*638G>C (PLCE1)	ENSP00000502340.1:n.*638G>C
ENST00000675718.1:c.3932G>C (PLCE1)
ENST00000676102.1:c.3550G>C (PLCE1)	ENSP00000502811.1:p.Gly1184Arg
ENST00000260766.7:c.4705G>C (PLCE1)	ENSP00000260766.3:p.Gly1569Arg
ENST00000371375.1:c.3781G>C (PLCE1)	ENSP00000360426.1:p.Gly1261Arg
ENST00000371380.7:c.4705G>C (PLCE1)	ENSP00000360431.2:p.Gly1569Arg
ENST00000371385.7:c.3781G>C (PLCE1)	ENSP00000360438.3:p.Gly1261Arg
NM_001165979.2:c.3781G>C (PLCE1)	NP_001159451.1:p.Gly1261Arg
NM_001288989.1:c.4657G>C (PLCE1)	NP_001275918.1:p.Gly1553Arg
NM_016341.3:c.4705G>C (PLCE1)	NP_057425.3:p.Gly1569Arg
NR_033969.1:n.877C>G (PLCE1-AS1)
XM_006717885.2:c.4705G>C (PLCE1)	XP_006717948.1:p.Gly1569Arg
XM_006717886.2:c.4705G>C (PLCE1)	XP_006717949.1:p.Gly1569Arg
XM_006717888.2:c.4705G>C (PLCE1)	XP_006717951.1:p.Gly1569Arg
XM_006717889.2:c.4657G>C (PLCE1)	XP_006717952.1:p.Gly1553Arg
XM_006717890.1:c.3781G>C (PLCE1)	XP_006717953.1:p.Gly1261Arg
XM_011539849.1:c.4705G>C (PLCE1)	XP_011538151.1:p.Gly1569Arg
XM_011539850.1:c.3550G>C (PLCE1)	XP_011538152.1:p.Gly1184Arg
XM_011539851.1:c.4705G>C (PLCE1)	XP_011538153.1:p.Gly1569Arg
XM_011539852.1:c.4705G>C (PLCE1)	XP_011538154.1:p.Gly1569Arg
XM_006717885.4:c.4705G>C (PLCE1)	XP_006717948.1:p.Gly1569Arg
XM_006717888.4:c.4705G>C (PLCE1)	XP_006717951.1:p.Gly1569Arg
XM_006717889.4:c.4657G>C (PLCE1)	XP_006717952.1:p.Gly1553Arg
XM_006717890.3:c.3781G>C (PLCE1)	XP_006717953.1:p.Gly1261Arg
XM_011539849.3:c.4705G>C (PLCE1)	XP_011538151.1:p.Gly1569Arg
XM_011539850.3:c.3550G>C (PLCE1)	XP_011538152.1:p.Gly1184Arg
XM_011539851.3:c.4705G>C (PLCE1)	XP_011538153.1:p.Gly1569Arg
XM_011539852.3:c.4705G>C (PLCE1)	XP_011538154.1:p.Gly1569Arg
XM_017016310.2:c.4705G>C (PLCE1)	XP_016871799.1:p.Gly1569Arg
XM_017016311.2:c.4705G>C (PLCE1)	XP_016871800.1:p.Gly1569Arg
XM_017016312.2:c.3733G>C (PLCE1)	XP_016871801.1:p.Gly1245Arg
NM_001288989.2:c.4657G>C (PLCE1)	NP_001275918.1:p.Gly1553Arg
NM_016341.4:c.4705G>C (PLCE1) MANE Select	NP_057425.3:p.Gly1569Arg