Canonical Allele Identifier: CA377642185

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058379T>G (hg19) ; chr10:g.94298622T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298622T>G , CM000672.2:g.94298622T>G	GRCh38
NC_000010.10:g.96058379T>G , CM000672.1:g.96058379T>G	GRCh37
NC_000010.9:g.96048369T>G	NCBI36
NG_015799.1:g.309634T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4487T>G	ENSP00000360426.1:p.Phe1496Cys
ENST00000685253.1:c.*1954T>G	ENSP00000509405.1:n.*1954T>G
ENST00000685889.1:n.2146T>G
ENST00000686807.1:n.830T>G
ENST00000686954.1:c.*695T>G	ENSP00000508416.1:n.*695T>G
ENST00000688810.1:c.4439T>G	ENSP00000509140.1:p.Phe1480Cys
ENST00000689233.1:n.9619T>G
ENST00000690340.1:n.3084T>G
ENST00000692286.1:c.5279T>G	ENSP00000509490.1:p.Phe1760Cys
ENST00000692396.1:c.5363T>G	ENSP00000508605.1:p.Phe1788Cys
ENST00000371380.8:c.5411T>G MANE Select	ENSP00000360431.2:p.Phe1804Cys
ENST00000371385.8:c.4385T>G	ENSP00000360438.4:p.Phe1462Cys
ENST00000674738.1:c.3966T>G
ENST00000674827.1:c.3527T>G	ENSP00000502523.1:p.Phe1176Cys
ENST00000675218.1:c.4487T>G	ENSP00000501910.1:p.Phe1496Cys
ENST00000675487.1:c.*1344T>G	ENSP00000502340.1:n.*1344T>G
ENST00000675718.1:c.4680T>G
ENST00000260766.7:c.5411T>G	ENSP00000260766.3:p.Phe1804Cys
ENST00000371375.1:c.4487T>G	ENSP00000360426.1:p.Phe1496Cys
ENST00000371380.7:c.5411T>G	ENSP00000360431.2:p.Phe1804Cys
ENST00000371385.7:c.4487T>G	ENSP00000360438.3:p.Phe1496Cys
NM_001165979.2:c.4487T>G	NP_001159451.1:p.Phe1496Cys
NM_001288989.1:c.5363T>G	NP_001275918.1:p.Phe1788Cys
NM_016341.3:c.5411T>G	NP_057425.3:p.Phe1804Cys
XM_006717885.2:c.5453T>G	XP_006717948.1:p.Phe1818Cys
XM_006717886.2:c.5453T>G	XP_006717949.1:p.Phe1818Cys
XM_006717888.2:c.5450T>G	XP_006717951.1:p.Phe1817Cys
XM_006717889.2:c.5405T>G	XP_006717952.1:p.Phe1802Cys
XM_006717890.1:c.4529T>G	XP_006717953.1:p.Phe1510Cys
XM_011539849.1:c.5453T>G	XP_011538151.1:p.Phe1818Cys
XM_011539850.1:c.4298T>G	XP_011538152.1:p.Phe1433Cys
XM_006717885.4:c.5453T>G	XP_006717948.1:p.Phe1818Cys
XM_006717888.4:c.5450T>G	XP_006717951.1:p.Phe1817Cys
XM_006717889.4:c.5405T>G	XP_006717952.1:p.Phe1802Cys
XM_006717890.3:c.4529T>G	XP_006717953.1:p.Phe1510Cys
XM_011539849.3:c.5453T>G	XP_011538151.1:p.Phe1818Cys
XM_011539850.3:c.4298T>G	XP_011538152.1:p.Phe1433Cys
XM_017016310.2:c.5453T>G	XP_016871799.1:p.Phe1818Cys
XM_017016311.2:c.5453T>G	XP_016871800.1:p.Phe1818Cys
XM_017016312.2:c.4439T>G	XP_016871801.1:p.Phe1480Cys
NM_001288989.2:c.5363T>G	NP_001275918.1:p.Phe1788Cys
NM_016341.4:c.5411T>G MANE Select	NP_057425.3:p.Phe1804Cys