Canonical Allele Identifier: CA470807584

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053347C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293590C>G , CM000672.2:g.94293590C>G	GRCh38
NC_000010.10:g.96053347C>G , CM000672.1:g.96053347C>G	GRCh37
NC_000010.9:g.96043337C>G	NCBI36
NG_015799.1:g.304602C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4194C>G	ENSP00000360426.1:p.Gly1398=
ENST00000685253.1:c.*1661C>G	ENSP00000509405.1:n.*1661C>G
ENST00000685889.1:n.1853C>G
ENST00000686807.1:n.537C>G
ENST00000686954.1:c.*402C>G	ENSP00000508416.1:n.*402C>G
ENST00000688810.1:c.4146C>G	ENSP00000509140.1:p.Gly1382=
ENST00000689233.1:n.9326C>G
ENST00000690340.1:n.2791C>G
ENST00000692286.1:c.5036-4789C>G	ENSP00000509490.1:n.5036-4789C>G
ENST00000692396.1:c.5070C>G	ENSP00000508605.1:p.Gly1690=
ENST00000371380.8:c.5118C>G MANE Select	ENSP00000360431.2:p.Gly1706=
ENST00000371385.8:c.4092C>G	ENSP00000360438.4:p.Gly1364=
ENST00000674738.1:c.3673C>G
ENST00000674827.1:c.3234C>G	ENSP00000502523.1:p.Gly1078=
ENST00000675218.1:c.4194C>G	ENSP00000501910.1:p.Gly1398=
ENST00000675487.1:c.*1051C>G	ENSP00000502340.1:n.*1051C>G
ENST00000675718.1:c.4387C>G
ENST00000676102.1:c.3963C>G	ENSP00000502811.1:p.Gly1321=
ENST00000260766.7:c.5118C>G	ENSP00000260766.3:p.Gly1706=
ENST00000371375.1:c.4194C>G	ENSP00000360426.1:p.Gly1398=
ENST00000371380.7:c.5118C>G	ENSP00000360431.2:p.Gly1706=
ENST00000371385.7:c.4194C>G	ENSP00000360438.3:p.Gly1398=
NM_001165979.2:c.4194C>G	NP_001159451.1:p.Gly1398=
NM_001288989.1:c.5070C>G	NP_001275918.1:p.Gly1690=
NM_016341.3:c.5118C>G	NP_057425.3:p.Gly1706=
XM_006717885.2:c.5160C>G	XP_006717948.1:p.Gly1720=
XM_006717886.2:c.5160C>G	XP_006717949.1:p.Gly1720=
XM_006717888.2:c.5157C>G	XP_006717951.1:p.Gly1719=
XM_006717889.2:c.5112C>G	XP_006717952.1:p.Gly1704=
XM_006717890.1:c.4236C>G	XP_006717953.1:p.Gly1412=
XM_011539849.1:c.5160C>G	XP_011538151.1:p.Gly1720=
XM_011539850.1:c.4005C>G	XP_011538152.1:p.Gly1335=
XM_006717885.4:c.5160C>G	XP_006717948.1:p.Gly1720=
XM_006717888.4:c.5157C>G	XP_006717951.1:p.Gly1719=
XM_006717889.4:c.5112C>G	XP_006717952.1:p.Gly1704=
XM_006717890.3:c.4236C>G	XP_006717953.1:p.Gly1412=
XM_011539849.3:c.5160C>G	XP_011538151.1:p.Gly1720=
XM_011539850.3:c.4005C>G	XP_011538152.1:p.Gly1335=
XM_017016310.2:c.5160C>G	XP_016871799.1:p.Gly1720=
XM_017016311.2:c.5160C>G	XP_016871800.1:p.Gly1720=
XM_017016312.2:c.4146C>G	XP_016871801.1:p.Gly1382=
NM_001288989.2:c.5070C>G	NP_001275918.1:p.Gly1690=
NM_016341.4:c.5118C>G MANE Select	NP_057425.3:p.Gly1706=