Canonical Allele Identifier: CA470815911

Gene: PLCE1 PLCE1-AS1

Linked Data

• MyVariant Identifiers: chr10:g.96039562A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94279805A>G , CM000672.2:g.94279805A>G	GRCh38
NC_000010.10:g.96039562A>G , CM000672.1:g.96039562A>G	GRCh37
NC_000010.9:g.96029552A>G	NCBI36
NG_015799.1:g.290817A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.3765A>G (PLCE1)	ENSP00000360426.1:p.Gln1255=
ENST00000685253.1:c.*1232A>G (PLCE1)	ENSP00000509405.1:n.*1232A>G
ENST00000685889.1:n.1424A>G (PLCE1)
ENST00000686954.1:c.4689A>G (PLCE1)	ENSP00000508416.1:p.Gln1563=
ENST00000688810.1:c.3717A>G (PLCE1)	ENSP00000509140.1:p.Gln1239=
ENST00000689233.1:n.5019A>G (PLCE1)
ENST00000692286.1:c.4689A>G (PLCE1)	ENSP00000509490.1:p.Gln1563=
ENST00000692396.1:c.4641A>G (PLCE1)	ENSP00000508605.1:p.Gln1547=
ENST00000371380.8:c.4689A>G (PLCE1) MANE Select	ENSP00000360431.2:p.Gln1563=
ENST00000371385.8:c.3663A>G (PLCE1)	ENSP00000360438.4:p.Gln1221=
ENST00000674738.1:c.3094A>G (PLCE1)
ENST00000674827.1:c.2766A>G (PLCE1)	ENSP00000502523.1:p.Gln922=
ENST00000675218.1:c.3765A>G (PLCE1)	ENSP00000501910.1:p.Gln1255=
ENST00000675487.1:c.*622A>G (PLCE1)	ENSP00000502340.1:n.*622A>G
ENST00000675718.1:c.3916A>G (PLCE1)
ENST00000676102.1:c.3534A>G (PLCE1)	ENSP00000502811.1:p.Gln1178=
ENST00000260766.7:c.4689A>G (PLCE1)	ENSP00000260766.3:p.Gln1563=
ENST00000371375.1:c.3765A>G (PLCE1)	ENSP00000360426.1:p.Gln1255=
ENST00000371380.7:c.4689A>G (PLCE1)	ENSP00000360431.2:p.Gln1563=
ENST00000371385.7:c.3765A>G (PLCE1)	ENSP00000360438.3:p.Gln1255=
NM_001165979.2:c.3765A>G (PLCE1)	NP_001159451.1:p.Gln1255=
NM_001288989.1:c.4641A>G (PLCE1)	NP_001275918.1:p.Gln1547=
NM_016341.3:c.4689A>G (PLCE1)	NP_057425.3:p.Gln1563=
NR_033969.1:n.893T>C (PLCE1-AS1)
XM_006717885.2:c.4689A>G (PLCE1)	XP_006717948.1:p.Gln1563=
XM_006717886.2:c.4689A>G (PLCE1)	XP_006717949.1:p.Gln1563=
XM_006717888.2:c.4689A>G (PLCE1)	XP_006717951.1:p.Gln1563=
XM_006717889.2:c.4641A>G (PLCE1)	XP_006717952.1:p.Gln1547=
XM_006717890.1:c.3765A>G (PLCE1)	XP_006717953.1:p.Gln1255=
XM_011539849.1:c.4689A>G (PLCE1)	XP_011538151.1:p.Gln1563=
XM_011539850.1:c.3534A>G (PLCE1)	XP_011538152.1:p.Gln1178=
XM_011539851.1:c.4689A>G (PLCE1)	XP_011538153.1:p.Gln1563=
XM_011539852.1:c.4689A>G (PLCE1)	XP_011538154.1:p.Gln1563=
XM_006717885.4:c.4689A>G (PLCE1)	XP_006717948.1:p.Gln1563=
XM_006717888.4:c.4689A>G (PLCE1)	XP_006717951.1:p.Gln1563=
XM_006717889.4:c.4641A>G (PLCE1)	XP_006717952.1:p.Gln1547=
XM_006717890.3:c.3765A>G (PLCE1)	XP_006717953.1:p.Gln1255=
XM_011539849.3:c.4689A>G (PLCE1)	XP_011538151.1:p.Gln1563=
XM_011539850.3:c.3534A>G (PLCE1)	XP_011538152.1:p.Gln1178=
XM_011539851.3:c.4689A>G (PLCE1)	XP_011538153.1:p.Gln1563=
XM_011539852.3:c.4689A>G (PLCE1)	XP_011538154.1:p.Gln1563=
XM_017016310.2:c.4689A>G (PLCE1)	XP_016871799.1:p.Gln1563=
XM_017016311.2:c.4689A>G (PLCE1)	XP_016871800.1:p.Gln1563=
XM_017016312.2:c.3717A>G (PLCE1)	XP_016871801.1:p.Gln1239=
NM_001288989.2:c.4641A>G (PLCE1)	NP_001275918.1:p.Gln1547=
NM_016341.4:c.4689A>G (PLCE1) MANE Select	NP_057425.3:p.Gln1563=