Canonical Allele Identifier: CA377641932

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058267C>A (hg19) ; chr10:g.94298510C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298510C>A , CM000672.2:g.94298510C>A	GRCh38
NC_000010.10:g.96058267C>A , CM000672.1:g.96058267C>A	GRCh37
NC_000010.9:g.96048257C>A	NCBI36
NG_015799.1:g.309522C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4375C>A	ENSP00000360426.1:p.Arg1459Ser
ENST00000685253.1:c.*1842C>A	ENSP00000509405.1:n.*1842C>A
ENST00000685889.1:n.2034C>A
ENST00000686807.1:n.718C>A
ENST00000686954.1:c.*583C>A	ENSP00000508416.1:n.*583C>A
ENST00000688810.1:c.4327C>A	ENSP00000509140.1:p.Arg1443Ser
ENST00000689233.1:n.9507C>A
ENST00000690340.1:n.2972C>A
ENST00000692286.1:c.5167C>A	ENSP00000509490.1:p.Arg1723Ser
ENST00000692396.1:c.5251C>A	ENSP00000508605.1:p.Arg1751Ser
ENST00000371380.8:c.5299C>A MANE Select	ENSP00000360431.2:p.Arg1767Ser
ENST00000371385.8:c.4273C>A	ENSP00000360438.4:p.Arg1425Ser
ENST00000674738.1:c.3854C>A
ENST00000674827.1:c.3415C>A	ENSP00000502523.1:p.Arg1139Ser
ENST00000675218.1:c.4375C>A	ENSP00000501910.1:p.Arg1459Ser
ENST00000675487.1:c.*1232C>A	ENSP00000502340.1:n.*1232C>A
ENST00000675718.1:c.4568C>A
ENST00000260766.7:c.5299C>A	ENSP00000260766.3:p.Arg1767Ser
ENST00000371375.1:c.4375C>A	ENSP00000360426.1:p.Arg1459Ser
ENST00000371380.7:c.5299C>A	ENSP00000360431.2:p.Arg1767Ser
ENST00000371385.7:c.4375C>A	ENSP00000360438.3:p.Arg1459Ser
NM_001165979.2:c.4375C>A	NP_001159451.1:p.Arg1459Ser
NM_001288989.1:c.5251C>A	NP_001275918.1:p.Arg1751Ser
NM_016341.3:c.5299C>A	NP_057425.3:p.Arg1767Ser
XM_006717885.2:c.5341C>A	XP_006717948.1:p.Arg1781Ser
XM_006717886.2:c.5341C>A	XP_006717949.1:p.Arg1781Ser
XM_006717888.2:c.5338C>A	XP_006717951.1:p.Arg1780Ser
XM_006717889.2:c.5293C>A	XP_006717952.1:p.Arg1765Ser
XM_006717890.1:c.4417C>A	XP_006717953.1:p.Arg1473Ser
XM_011539849.1:c.5341C>A	XP_011538151.1:p.Arg1781Ser
XM_011539850.1:c.4186C>A	XP_011538152.1:p.Arg1396Ser
XM_006717885.4:c.5341C>A	XP_006717948.1:p.Arg1781Ser
XM_006717888.4:c.5338C>A	XP_006717951.1:p.Arg1780Ser
XM_006717889.4:c.5293C>A	XP_006717952.1:p.Arg1765Ser
XM_006717890.3:c.4417C>A	XP_006717953.1:p.Arg1473Ser
XM_011539849.3:c.5341C>A	XP_011538151.1:p.Arg1781Ser
XM_011539850.3:c.4186C>A	XP_011538152.1:p.Arg1396Ser
XM_017016310.2:c.5341C>A	XP_016871799.1:p.Arg1781Ser
XM_017016311.2:c.5341C>A	XP_016871800.1:p.Arg1781Ser
XM_017016312.2:c.4327C>A	XP_016871801.1:p.Arg1443Ser
NM_001288989.2:c.5251C>A	NP_001275918.1:p.Arg1751Ser
NM_016341.4:c.5299C>A MANE Select	NP_057425.3:p.Arg1767Ser