Canonical Allele Identifier: CA377642125

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058360A>C (hg19) ; chr10:g.94298603A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298603A>C , CM000672.2:g.94298603A>C	GRCh38
NC_000010.10:g.96058360A>C , CM000672.1:g.96058360A>C	GRCh37
NC_000010.9:g.96048350A>C	NCBI36
NG_015799.1:g.309615A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4468A>C	ENSP00000360426.1:p.Asn1490His
ENST00000685253.1:c.*1935A>C	ENSP00000509405.1:n.*1935A>C
ENST00000685889.1:n.2127A>C
ENST00000686807.1:n.811A>C
ENST00000686954.1:c.*676A>C	ENSP00000508416.1:n.*676A>C
ENST00000688810.1:c.4420A>C	ENSP00000509140.1:p.Asn1474His
ENST00000689233.1:n.9600A>C
ENST00000690340.1:n.3065A>C
ENST00000692286.1:c.5260A>C	ENSP00000509490.1:p.Asn1754His
ENST00000692396.1:c.5344A>C	ENSP00000508605.1:p.Asn1782His
ENST00000371380.8:c.5392A>C MANE Select	ENSP00000360431.2:p.Asn1798His
ENST00000371385.8:c.4366A>C	ENSP00000360438.4:p.Asn1456His
ENST00000674738.1:c.3947A>C
ENST00000674827.1:c.3508A>C	ENSP00000502523.1:p.Asn1170His
ENST00000675218.1:c.4468A>C	ENSP00000501910.1:p.Asn1490His
ENST00000675487.1:c.*1325A>C	ENSP00000502340.1:n.*1325A>C
ENST00000675718.1:c.4661A>C
ENST00000260766.7:c.5392A>C	ENSP00000260766.3:p.Asn1798His
ENST00000371375.1:c.4468A>C	ENSP00000360426.1:p.Asn1490His
ENST00000371380.7:c.5392A>C	ENSP00000360431.2:p.Asn1798His
ENST00000371385.7:c.4468A>C	ENSP00000360438.3:p.Asn1490His
NM_001165979.2:c.4468A>C	NP_001159451.1:p.Asn1490His
NM_001288989.1:c.5344A>C	NP_001275918.1:p.Asn1782His
NM_016341.3:c.5392A>C	NP_057425.3:p.Asn1798His
XM_006717885.2:c.5434A>C	XP_006717948.1:p.Asn1812His
XM_006717886.2:c.5434A>C	XP_006717949.1:p.Asn1812His
XM_006717888.2:c.5431A>C	XP_006717951.1:p.Asn1811His
XM_006717889.2:c.5386A>C	XP_006717952.1:p.Asn1796His
XM_006717890.1:c.4510A>C	XP_006717953.1:p.Asn1504His
XM_011539849.1:c.5434A>C	XP_011538151.1:p.Asn1812His
XM_011539850.1:c.4279A>C	XP_011538152.1:p.Asn1427His
XM_006717885.4:c.5434A>C	XP_006717948.1:p.Asn1812His
XM_006717888.4:c.5431A>C	XP_006717951.1:p.Asn1811His
XM_006717889.4:c.5386A>C	XP_006717952.1:p.Asn1796His
XM_006717890.3:c.4510A>C	XP_006717953.1:p.Asn1504His
XM_011539849.3:c.5434A>C	XP_011538151.1:p.Asn1812His
XM_011539850.3:c.4279A>C	XP_011538152.1:p.Asn1427His
XM_017016310.2:c.5434A>C	XP_016871799.1:p.Asn1812His
XM_017016311.2:c.5434A>C	XP_016871800.1:p.Asn1812His
XM_017016312.2:c.4420A>C	XP_016871801.1:p.Asn1474His
NM_001288989.2:c.5344A>C	NP_001275918.1:p.Asn1782His
NM_016341.4:c.5392A>C MANE Select	NP_057425.3:p.Asn1798His