Canonical Allele Identifier: CA377641983

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058291A>G (hg19) ; chr10:g.94298534A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298534A>G , CM000672.2:g.94298534A>G	GRCh38
NC_000010.10:g.96058291A>G , CM000672.1:g.96058291A>G	GRCh37
NC_000010.9:g.96048281A>G	NCBI36
NG_015799.1:g.309546A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4399A>G	ENSP00000360426.1:p.Lys1467Glu
ENST00000685253.1:c.*1866A>G	ENSP00000509405.1:n.*1866A>G
ENST00000685889.1:n.2058A>G
ENST00000686807.1:n.742A>G
ENST00000686954.1:c.*607A>G	ENSP00000508416.1:n.*607A>G
ENST00000688810.1:c.4351A>G	ENSP00000509140.1:p.Lys1451Glu
ENST00000689233.1:n.9531A>G
ENST00000690340.1:n.2996A>G
ENST00000692286.1:c.5191A>G	ENSP00000509490.1:p.Lys1731Glu
ENST00000692396.1:c.5275A>G	ENSP00000508605.1:p.Lys1759Glu
ENST00000371380.8:c.5323A>G MANE Select	ENSP00000360431.2:p.Lys1775Glu
ENST00000371385.8:c.4297A>G	ENSP00000360438.4:p.Lys1433Glu
ENST00000674738.1:c.3878A>G
ENST00000674827.1:c.3439A>G	ENSP00000502523.1:p.Lys1147Glu
ENST00000675218.1:c.4399A>G	ENSP00000501910.1:p.Lys1467Glu
ENST00000675487.1:c.*1256A>G	ENSP00000502340.1:n.*1256A>G
ENST00000675718.1:c.4592A>G
ENST00000260766.7:c.5323A>G	ENSP00000260766.3:p.Lys1775Glu
ENST00000371375.1:c.4399A>G	ENSP00000360426.1:p.Lys1467Glu
ENST00000371380.7:c.5323A>G	ENSP00000360431.2:p.Lys1775Glu
ENST00000371385.7:c.4399A>G	ENSP00000360438.3:p.Lys1467Glu
NM_001165979.2:c.4399A>G	NP_001159451.1:p.Lys1467Glu
NM_001288989.1:c.5275A>G	NP_001275918.1:p.Lys1759Glu
NM_016341.3:c.5323A>G	NP_057425.3:p.Lys1775Glu
XM_006717885.2:c.5365A>G	XP_006717948.1:p.Lys1789Glu
XM_006717886.2:c.5365A>G	XP_006717949.1:p.Lys1789Glu
XM_006717888.2:c.5362A>G	XP_006717951.1:p.Lys1788Glu
XM_006717889.2:c.5317A>G	XP_006717952.1:p.Lys1773Glu
XM_006717890.1:c.4441A>G	XP_006717953.1:p.Lys1481Glu
XM_011539849.1:c.5365A>G	XP_011538151.1:p.Lys1789Glu
XM_011539850.1:c.4210A>G	XP_011538152.1:p.Lys1404Glu
XM_006717885.4:c.5365A>G	XP_006717948.1:p.Lys1789Glu
XM_006717888.4:c.5362A>G	XP_006717951.1:p.Lys1788Glu
XM_006717889.4:c.5317A>G	XP_006717952.1:p.Lys1773Glu
XM_006717890.3:c.4441A>G	XP_006717953.1:p.Lys1481Glu
XM_011539849.3:c.5365A>G	XP_011538151.1:p.Lys1789Glu
XM_011539850.3:c.4210A>G	XP_011538152.1:p.Lys1404Glu
XM_017016310.2:c.5365A>G	XP_016871799.1:p.Lys1789Glu
XM_017016311.2:c.5365A>G	XP_016871800.1:p.Lys1789Glu
XM_017016312.2:c.4351A>G	XP_016871801.1:p.Lys1451Glu
NM_001288989.2:c.5275A>G	NP_001275918.1:p.Lys1759Glu
NM_016341.4:c.5323A>G MANE Select	NP_057425.3:p.Lys1775Glu