Canonical Allele Identifier: CA377641937

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058270C>A (hg19) ; chr10:g.94298513C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298513C>A , CM000672.2:g.94298513C>A	GRCh38
NC_000010.10:g.96058270C>A , CM000672.1:g.96058270C>A	GRCh37
NC_000010.9:g.96048260C>A	NCBI36
NG_015799.1:g.309525C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4378C>A	ENSP00000360426.1:p.Leu1460Met
ENST00000685253.1:c.*1845C>A	ENSP00000509405.1:n.*1845C>A
ENST00000685889.1:n.2037C>A
ENST00000686807.1:n.721C>A
ENST00000686954.1:c.*586C>A	ENSP00000508416.1:n.*586C>A
ENST00000688810.1:c.4330C>A	ENSP00000509140.1:p.Leu1444Met
ENST00000689233.1:n.9510C>A
ENST00000690340.1:n.2975C>A
ENST00000692286.1:c.5170C>A	ENSP00000509490.1:p.Leu1724Met
ENST00000692396.1:c.5254C>A	ENSP00000508605.1:p.Leu1752Met
ENST00000371380.8:c.5302C>A MANE Select	ENSP00000360431.2:p.Leu1768Met
ENST00000371385.8:c.4276C>A	ENSP00000360438.4:p.Leu1426Met
ENST00000674738.1:c.3857C>A
ENST00000674827.1:c.3418C>A	ENSP00000502523.1:p.Leu1140Met
ENST00000675218.1:c.4378C>A	ENSP00000501910.1:p.Leu1460Met
ENST00000675487.1:c.*1235C>A	ENSP00000502340.1:n.*1235C>A
ENST00000675718.1:c.4571C>A
ENST00000260766.7:c.5302C>A	ENSP00000260766.3:p.Leu1768Met
ENST00000371375.1:c.4378C>A	ENSP00000360426.1:p.Leu1460Met
ENST00000371380.7:c.5302C>A	ENSP00000360431.2:p.Leu1768Met
ENST00000371385.7:c.4378C>A	ENSP00000360438.3:p.Leu1460Met
NM_001165979.2:c.4378C>A	NP_001159451.1:p.Leu1460Met
NM_001288989.1:c.5254C>A	NP_001275918.1:p.Leu1752Met
NM_016341.3:c.5302C>A	NP_057425.3:p.Leu1768Met
XM_006717885.2:c.5344C>A	XP_006717948.1:p.Leu1782Met
XM_006717886.2:c.5344C>A	XP_006717949.1:p.Leu1782Met
XM_006717888.2:c.5341C>A	XP_006717951.1:p.Leu1781Met
XM_006717889.2:c.5296C>A	XP_006717952.1:p.Leu1766Met
XM_006717890.1:c.4420C>A	XP_006717953.1:p.Leu1474Met
XM_011539849.1:c.5344C>A	XP_011538151.1:p.Leu1782Met
XM_011539850.1:c.4189C>A	XP_011538152.1:p.Leu1397Met
XM_006717885.4:c.5344C>A	XP_006717948.1:p.Leu1782Met
XM_006717888.4:c.5341C>A	XP_006717951.1:p.Leu1781Met
XM_006717889.4:c.5296C>A	XP_006717952.1:p.Leu1766Met
XM_006717890.3:c.4420C>A	XP_006717953.1:p.Leu1474Met
XM_011539849.3:c.5344C>A	XP_011538151.1:p.Leu1782Met
XM_011539850.3:c.4189C>A	XP_011538152.1:p.Leu1397Met
XM_017016310.2:c.5344C>A	XP_016871799.1:p.Leu1782Met
XM_017016311.2:c.5344C>A	XP_016871800.1:p.Leu1782Met
XM_017016312.2:c.4330C>A	XP_016871801.1:p.Leu1444Met
NM_001288989.2:c.5254C>A	NP_001275918.1:p.Leu1752Met
NM_016341.4:c.5302C>A MANE Select	NP_057425.3:p.Leu1768Met