Canonical Allele Identifier: CA377641811

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058213A>G (hg19) ; chr10:g.94298456A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298456A>G , CM000672.2:g.94298456A>G	GRCh38
NC_000010.10:g.96058213A>G , CM000672.1:g.96058213A>G	GRCh37
NC_000010.9:g.96048203A>G	NCBI36
NG_015799.1:g.309468A>G

Transcript Alleles

HGVS	Amino-acid change
NM_001165979.2:c.4321A>G	NP_001159451.1:p.Ile1441Val
NM_001288989.1:c.5197A>G	NP_001275918.1:p.Ile1733Val
NM_016341.3:c.5245A>G	NP_057425.3:p.Ile1749Val
XM_006717885.2:c.5287A>G	XP_006717948.1:p.Ile1763Val
XM_006717886.2:c.5287A>G	XP_006717949.1:p.Ile1763Val
XM_006717888.2:c.5284A>G	XP_006717951.1:p.Ile1762Val
XM_006717889.2:c.5239A>G	XP_006717952.1:p.Ile1747Val
XM_006717890.1:c.4363A>G	XP_006717953.1:p.Ile1455Val
XM_011539849.1:c.5287A>G	XP_011538151.1:p.Ile1763Val
XM_011539850.1:c.4132A>G	XP_011538152.1:p.Ile1378Val
XM_006717885.4:c.5287A>G	XP_006717948.1:p.Ile1763Val
XM_006717888.4:c.5284A>G	XP_006717951.1:p.Ile1762Val
XM_006717889.4:c.5239A>G	XP_006717952.1:p.Ile1747Val
XM_006717890.3:c.4363A>G	XP_006717953.1:p.Ile1455Val
XM_011539849.3:c.5287A>G	XP_011538151.1:p.Ile1763Val
XM_011539850.3:c.4132A>G	XP_011538152.1:p.Ile1378Val
XM_017016310.2:c.5287A>G	XP_016871799.1:p.Ile1763Val
XM_017016311.2:c.5287A>G	XP_016871800.1:p.Ile1763Val
XM_017016312.2:c.4273A>G	XP_016871801.1:p.Ile1425Val
NM_001288989.2:c.5197A>G	NP_001275918.1:p.Ile1733Val
NM_016341.4:c.5245A>G MANE Select	NP_057425.3:p.Ile1749Val
ENST00000260766.7:c.5245A>G	ENSP00000260766.3:p.Ile1749Val
ENST00000371375.1:n.4321A>G	ENSP00000360426.1:p.Ile1441Val
ENST00000371380.7:c.5245A>G	ENSP00000360431.2:p.Ile1749Val
ENST00000371385.7:c.4321A>G	ENSP00000360438.3:p.Ile1441Val