Canonical Allele Identifier: CA470986407

Gene: PLCE1

Linked Data

• gnomAD v4: 10-94298398-A-G
• MyVariant Identifiers: chr10:g.96058155A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298398A>G , CM000672.2:g.94298398A>G	GRCh38
NC_000010.10:g.96058155A>G , CM000672.1:g.96058155A>G	GRCh37
NC_000010.9:g.96048145A>G	NCBI36
NG_015799.1:g.309410A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4263A>G	ENSP00000360426.1:p.Arg1421=
ENST00000685253.1:c.*1730A>G	ENSP00000509405.1:n.*1730A>G
ENST00000685889.1:n.1922A>G
ENST00000686807.1:n.606A>G
ENST00000686954.1:c.*471A>G	ENSP00000508416.1:n.*471A>G
ENST00000688810.1:c.4215A>G	ENSP00000509140.1:p.Arg1405=
ENST00000689233.1:n.9395A>G
ENST00000690340.1:n.2860A>G
ENST00000692286.1:c.5055A>G	ENSP00000509490.1:p.Arg1685=
ENST00000692396.1:c.5139A>G	ENSP00000508605.1:p.Arg1713=
ENST00000371380.8:c.5187A>G MANE Select	ENSP00000360431.2:p.Arg1729=
ENST00000371385.8:c.4161A>G	ENSP00000360438.4:p.Arg1387=
ENST00000674738.1:c.3742A>G
ENST00000674827.1:c.3303A>G	ENSP00000502523.1:p.Arg1101=
ENST00000675218.1:c.4263A>G	ENSP00000501910.1:p.Arg1421=
ENST00000675487.1:c.*1120A>G	ENSP00000502340.1:n.*1120A>G
ENST00000675718.1:c.4456A>G
ENST00000676102.1:c.4032A>G	ENSP00000502811.1:p.Arg1344=
ENST00000260766.7:c.5187A>G	ENSP00000260766.3:p.Arg1729=
ENST00000371375.1:c.4263A>G	ENSP00000360426.1:p.Arg1421=
ENST00000371380.7:c.5187A>G	ENSP00000360431.2:p.Arg1729=
ENST00000371385.7:c.4263A>G	ENSP00000360438.3:p.Arg1421=
NM_001165979.2:c.4263A>G	NP_001159451.1:p.Arg1421=
NM_001288989.1:c.5139A>G	NP_001275918.1:p.Arg1713=
NM_016341.3:c.5187A>G	NP_057425.3:p.Arg1729=
XM_006717885.2:c.5229A>G	XP_006717948.1:p.Arg1743=
XM_006717886.2:c.5229A>G	XP_006717949.1:p.Arg1743=
XM_006717888.2:c.5226A>G	XP_006717951.1:p.Arg1742=
XM_006717889.2:c.5181A>G	XP_006717952.1:p.Arg1727=
XM_006717890.1:c.4305A>G	XP_006717953.1:p.Arg1435=
XM_011539849.1:c.5229A>G	XP_011538151.1:p.Arg1743=
XM_011539850.1:c.4074A>G	XP_011538152.1:p.Arg1358=
XM_006717885.4:c.5229A>G	XP_006717948.1:p.Arg1743=
XM_006717888.4:c.5226A>G	XP_006717951.1:p.Arg1742=
XM_006717889.4:c.5181A>G	XP_006717952.1:p.Arg1727=
XM_006717890.3:c.4305A>G	XP_006717953.1:p.Arg1435=
XM_011539849.3:c.5229A>G	XP_011538151.1:p.Arg1743=
XM_011539850.3:c.4074A>G	XP_011538152.1:p.Arg1358=
XM_017016310.2:c.5229A>G	XP_016871799.1:p.Arg1743=
XM_017016311.2:c.5229A>G	XP_016871800.1:p.Arg1743=
XM_017016312.2:c.4215A>G	XP_016871801.1:p.Arg1405=
NM_001288989.2:c.5139A>G	NP_001275918.1:p.Arg1713=
NM_016341.4:c.5187A>G MANE Select	NP_057425.3:p.Arg1729=