Canonical Allele Identifier: CA377641862

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058234C>G (hg19) ; chr10:g.94298477C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298477C>G , CM000672.2:g.94298477C>G	GRCh38
NC_000010.10:g.96058234C>G , CM000672.1:g.96058234C>G	GRCh37
NC_000010.9:g.96048224C>G	NCBI36
NG_015799.1:g.309489C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4342C>G	ENSP00000360426.1:p.His1448Asp
ENST00000685253.1:c.*1809C>G	ENSP00000509405.1:n.*1809C>G
ENST00000685889.1:n.2001C>G
ENST00000686807.1:n.685C>G
ENST00000686954.1:c.*550C>G	ENSP00000508416.1:n.*550C>G
ENST00000688810.1:c.4294C>G	ENSP00000509140.1:p.His1432Asp
ENST00000689233.1:n.9474C>G
ENST00000690340.1:n.2939C>G
ENST00000692286.1:c.5134C>G	ENSP00000509490.1:p.His1712Asp
ENST00000692396.1:c.5218C>G	ENSP00000508605.1:p.His1740Asp
ENST00000371380.8:c.5266C>G MANE Select	ENSP00000360431.2:p.His1756Asp
ENST00000371385.8:c.4240C>G	ENSP00000360438.4:p.His1414Asp
ENST00000674738.1:c.3821C>G
ENST00000674827.1:c.3382C>G	ENSP00000502523.1:p.His1128Asp
ENST00000675218.1:c.4342C>G	ENSP00000501910.1:p.His1448Asp
ENST00000675487.1:c.*1199C>G	ENSP00000502340.1:n.*1199C>G
ENST00000675718.1:c.4535C>G
ENST00000676102.1:c.4111C>G
ENST00000260766.7:c.5266C>G	ENSP00000260766.3:p.His1756Asp
ENST00000371375.1:c.4342C>G	ENSP00000360426.1:p.His1448Asp
ENST00000371380.7:c.5266C>G	ENSP00000360431.2:p.His1756Asp
ENST00000371385.7:c.4342C>G	ENSP00000360438.3:p.His1448Asp
NM_001165979.2:c.4342C>G	NP_001159451.1:p.His1448Asp
NM_001288989.1:c.5218C>G	NP_001275918.1:p.His1740Asp
NM_016341.3:c.5266C>G	NP_057425.3:p.His1756Asp
XM_006717885.2:c.5308C>G	XP_006717948.1:p.His1770Asp
XM_006717886.2:c.5308C>G	XP_006717949.1:p.His1770Asp
XM_006717888.2:c.5305C>G	XP_006717951.1:p.His1769Asp
XM_006717889.2:c.5260C>G	XP_006717952.1:p.His1754Asp
XM_006717890.1:c.4384C>G	XP_006717953.1:p.His1462Asp
XM_011539849.1:c.5308C>G	XP_011538151.1:p.His1770Asp
XM_011539850.1:c.4153C>G	XP_011538152.1:p.His1385Asp
XM_006717885.4:c.5308C>G	XP_006717948.1:p.His1770Asp
XM_006717888.4:c.5305C>G	XP_006717951.1:p.His1769Asp
XM_006717889.4:c.5260C>G	XP_006717952.1:p.His1754Asp
XM_006717890.3:c.4384C>G	XP_006717953.1:p.His1462Asp
XM_011539849.3:c.5308C>G	XP_011538151.1:p.His1770Asp
XM_011539850.3:c.4153C>G	XP_011538152.1:p.His1385Asp
XM_017016310.2:c.5308C>G	XP_016871799.1:p.His1770Asp
XM_017016311.2:c.5308C>G	XP_016871800.1:p.His1770Asp
XM_017016312.2:c.4294C>G	XP_016871801.1:p.His1432Asp
NM_001288989.2:c.5218C>G	NP_001275918.1:p.His1740Asp
NM_016341.4:c.5266C>G MANE Select	NP_057425.3:p.His1756Asp