Canonical Allele Identifier: CA377641682

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058150A>G (hg19) ; chr10:g.94298393A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298393A>G , CM000672.2:g.94298393A>G	GRCh38
NC_000010.10:g.96058150A>G , CM000672.1:g.96058150A>G	GRCh37
NC_000010.9:g.96048140A>G	NCBI36
NG_015799.1:g.309405A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:n.4258A>G	ENSP00000360426.1:p.Ile1420Val
ENST00000685253.1:c.*1725A>G	ENSP00000509405.1:n.*1725A>G
ENST00000685889.1:n.1917A>G
ENST00000686807.1:n.601A>G
ENST00000686954.1:c.*466A>G	ENSP00000508416.1:n.*466A>G
ENST00000688810.1:n.4210A>G	ENSP00000509140.1:p.Ile1404Val
ENST00000689233.1:n.9390A>G
ENST00000690340.1:n.2855A>G
ENST00000692286.1:c.5050A>G	ENSP00000509490.1:p.Ile1684Val
ENST00000692396.1:c.5134A>G	ENSP00000508605.1:p.Ile1712Val
ENST00000371380.8:c.5182A>G MANE Select	ENSP00000360431.2:p.Ile1728Val
ENST00000371385.8:c.4156A>G	ENSP00000360438.4:p.Ile1386Val
ENST00000674738.1:n.3737A>G
ENST00000674827.1:n.3298A>G	ENSP00000502523.1:p.Ile1100Val
ENST00000675218.1:n.4258A>G	ENSP00000501910.1:p.Ile1420Val
ENST00000675487.1:c.*1115A>G	ENSP00000502340.1:n.*1115A>G
ENST00000675718.1:n.4451A>G
ENST00000676102.1:c.4027A>G	ENSP00000502811.1:p.Ile1343Val
ENST00000260766.7:c.5182A>G	ENSP00000260766.3:p.Ile1728Val
ENST00000371375.1:n.4258A>G	ENSP00000360426.1:p.Ile1420Val
ENST00000371380.7:c.5182A>G	ENSP00000360431.2:p.Ile1728Val
ENST00000371385.7:c.4258A>G	ENSP00000360438.3:p.Ile1420Val
NM_001165979.2:c.4258A>G	NP_001159451.1:p.Ile1420Val
NM_001288989.1:c.5134A>G	NP_001275918.1:p.Ile1712Val
NM_016341.3:c.5182A>G	NP_057425.3:p.Ile1728Val
XM_006717885.2:c.5224A>G	XP_006717948.1:p.Ile1742Val
XM_006717886.2:c.5224A>G	XP_006717949.1:p.Ile1742Val
XM_006717888.2:c.5221A>G	XP_006717951.1:p.Ile1741Val
XM_006717889.2:c.5176A>G	XP_006717952.1:p.Ile1726Val
XM_006717890.1:c.4300A>G	XP_006717953.1:p.Ile1434Val
XM_011539849.1:c.5224A>G	XP_011538151.1:p.Ile1742Val
XM_011539850.1:c.4069A>G	XP_011538152.1:p.Ile1357Val
XM_006717885.4:c.5224A>G	XP_006717948.1:p.Ile1742Val
XM_006717888.4:c.5221A>G	XP_006717951.1:p.Ile1741Val
XM_006717889.4:c.5176A>G	XP_006717952.1:p.Ile1726Val
XM_006717890.3:c.4300A>G	XP_006717953.1:p.Ile1434Val
XM_011539849.3:c.5224A>G	XP_011538151.1:p.Ile1742Val
XM_011539850.3:c.4069A>G	XP_011538152.1:p.Ile1357Val
XM_017016310.2:c.5224A>G	XP_016871799.1:p.Ile1742Val
XM_017016311.2:c.5224A>G	XP_016871800.1:p.Ile1742Val
XM_017016312.2:c.4210A>G	XP_016871801.1:p.Ile1404Val
NM_001288989.2:c.5134A>G	NP_001275918.1:p.Ile1712Val
NM_016341.4:c.5182A>G MANE Select	NP_057425.3:p.Ile1728Val