Canonical Allele Identifier: CA377641653

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058137T>A (hg19) ; chr10:g.94298380T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298380T>A , CM000672.2:g.94298380T>A	GRCh38
NC_000010.10:g.96058137T>A , CM000672.1:g.96058137T>A	GRCh37
NC_000010.9:g.96048127T>A	NCBI36
NG_015799.1:g.309392T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4245T>A	ENSP00000360426.1:p.Ser1415Arg
ENST00000685253.1:c.*1712T>A	ENSP00000509405.1:n.*1712T>A
ENST00000685889.1:n.1904T>A
ENST00000686807.1:n.588T>A
ENST00000686954.1:c.*453T>A	ENSP00000508416.1:n.*453T>A
ENST00000688810.1:c.4197T>A	ENSP00000509140.1:p.Ser1399Arg
ENST00000689233.1:n.9377T>A
ENST00000690340.1:n.2842T>A
ENST00000692286.1:c.5037T>A	ENSP00000509490.1:p.Gly1679=
ENST00000692396.1:c.5121T>A	ENSP00000508605.1:p.Ser1707Arg
ENST00000371380.8:c.5169T>A MANE Select	ENSP00000360431.2:p.Ser1723Arg
ENST00000371385.8:c.4143T>A	ENSP00000360438.4:p.Ser1381Arg
ENST00000674738.1:c.3724T>A
ENST00000674827.1:c.3285T>A	ENSP00000502523.1:p.Ser1095Arg
ENST00000675218.1:c.4245T>A	ENSP00000501910.1:p.Ser1415Arg
ENST00000675487.1:c.*1102T>A	ENSP00000502340.1:n.*1102T>A
ENST00000675718.1:c.4438T>A
ENST00000676102.1:c.4014T>A	ENSP00000502811.1:p.Ser1338Arg
ENST00000260766.7:c.5169T>A	ENSP00000260766.3:p.Ser1723Arg
ENST00000371375.1:c.4245T>A	ENSP00000360426.1:p.Ser1415Arg
ENST00000371380.7:c.5169T>A	ENSP00000360431.2:p.Ser1723Arg
ENST00000371385.7:c.4245T>A	ENSP00000360438.3:p.Ser1415Arg
NM_001165979.2:c.4245T>A	NP_001159451.1:p.Ser1415Arg
NM_001288989.1:c.5121T>A	NP_001275918.1:p.Ser1707Arg
NM_016341.3:c.5169T>A	NP_057425.3:p.Ser1723Arg
XM_006717885.2:c.5211T>A	XP_006717948.1:p.Ser1737Arg
XM_006717886.2:c.5211T>A	XP_006717949.1:p.Ser1737Arg
XM_006717888.2:c.5208T>A	XP_006717951.1:p.Ser1736Arg
XM_006717889.2:c.5163T>A	XP_006717952.1:p.Ser1721Arg
XM_006717890.1:c.4287T>A	XP_006717953.1:p.Ser1429Arg
XM_011539849.1:c.5211T>A	XP_011538151.1:p.Ser1737Arg
XM_011539850.1:c.4056T>A	XP_011538152.1:p.Ser1352Arg
XM_006717885.4:c.5211T>A	XP_006717948.1:p.Ser1737Arg
XM_006717888.4:c.5208T>A	XP_006717951.1:p.Ser1736Arg
XM_006717889.4:c.5163T>A	XP_006717952.1:p.Ser1721Arg
XM_006717890.3:c.4287T>A	XP_006717953.1:p.Ser1429Arg
XM_011539849.3:c.5211T>A	XP_011538151.1:p.Ser1737Arg
XM_011539850.3:c.4056T>A	XP_011538152.1:p.Ser1352Arg
XM_017016310.2:c.5211T>A	XP_016871799.1:p.Ser1737Arg
XM_017016311.2:c.5211T>A	XP_016871800.1:p.Ser1737Arg
XM_017016312.2:c.4197T>A	XP_016871801.1:p.Ser1399Arg
NM_001288989.2:c.5121T>A	NP_001275918.1:p.Ser1707Arg
NM_016341.4:c.5169T>A MANE Select	NP_057425.3:p.Ser1723Arg