Canonical Allele Identifier: CA470986455

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058203C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298446C>G , CM000672.2:g.94298446C>G	GRCh38
NC_000010.10:g.96058203C>G , CM000672.1:g.96058203C>G	GRCh37
NC_000010.9:g.96048193C>G	NCBI36
NG_015799.1:g.309458C>G

Transcript Alleles

HGVS	Amino-acid change
NM_001165979.2:c.4311C>G	NP_001159451.1:p.Leu1437=
NM_001288989.1:c.5187C>G	NP_001275918.1:p.Leu1729=
NM_016341.3:c.5235C>G	NP_057425.3:p.Leu1745=
XM_006717885.2:c.5277C>G	XP_006717948.1:p.Leu1759=
XM_006717886.2:c.5277C>G	XP_006717949.1:p.Leu1759=
XM_006717888.2:c.5274C>G	XP_006717951.1:p.Leu1758=
XM_006717889.2:c.5229C>G	XP_006717952.1:p.Leu1743=
XM_006717890.1:c.4353C>G	XP_006717953.1:p.Leu1451=
XM_011539849.1:c.5277C>G	XP_011538151.1:p.Leu1759=
XM_011539850.1:c.4122C>G	XP_011538152.1:p.Leu1374=
XM_006717885.4:c.5277C>G	XP_006717948.1:p.Leu1759=
XM_006717888.4:c.5274C>G	XP_006717951.1:p.Leu1758=
XM_006717889.4:c.5229C>G	XP_006717952.1:p.Leu1743=
XM_006717890.3:c.4353C>G	XP_006717953.1:p.Leu1451=
XM_011539849.3:c.5277C>G	XP_011538151.1:p.Leu1759=
XM_011539850.3:c.4122C>G	XP_011538152.1:p.Leu1374=
XM_017016310.2:c.5277C>G	XP_016871799.1:p.Leu1759=
XM_017016311.2:c.5277C>G	XP_016871800.1:p.Leu1759=
XM_017016312.2:c.4263C>G	XP_016871801.1:p.Leu1421=
NM_001288989.2:c.5187C>G	NP_001275918.1:p.Leu1729=
NM_016341.4:c.5235C>G MANE Select	NP_057425.3:p.Leu1745=
ENST00000260766.7:c.5235C>G	ENSP00000260766.3:p.Leu1745=
ENST00000371375.1:n.4311C>G	ENSP00000360426.1:p.Leu1437=
ENST00000371380.7:c.5235C>G	ENSP00000360431.2:p.Leu1745=
ENST00000371385.7:c.4311C>G	ENSP00000360438.3:p.Leu1437=