Canonical Allele Identifier: CA377642126

Gene: PLCE1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4468A>G	ENSP00000360426.1:p.Asn1490Asp
ENST00000685253.1:c.*1935A>G	ENSP00000509405.1:n.*1935A>G
ENST00000685889.1:n.2127A>G
ENST00000686807.1:n.811A>G
ENST00000686954.1:c.*676A>G	ENSP00000508416.1:n.*676A>G
ENST00000688810.1:c.4420A>G	ENSP00000509140.1:p.Asn1474Asp
ENST00000689233.1:n.9600A>G
ENST00000690340.1:n.3065A>G
ENST00000692286.1:c.5260A>G	ENSP00000509490.1:p.Asn1754Asp
ENST00000692396.1:c.5344A>G	ENSP00000508605.1:p.Asn1782Asp
ENST00000371380.8:c.5392A>G MANE Select	ENSP00000360431.2:p.Asn1798Asp
ENST00000371385.8:c.4366A>G	ENSP00000360438.4:p.Asn1456Asp
ENST00000674738.1:c.3947A>G
ENST00000674827.1:c.3508A>G	ENSP00000502523.1:p.Asn1170Asp
ENST00000675218.1:c.4468A>G	ENSP00000501910.1:p.Asn1490Asp
ENST00000675487.1:c.*1325A>G	ENSP00000502340.1:n.*1325A>G
ENST00000675718.1:c.4661A>G
ENST00000260766.7:c.5392A>G	ENSP00000260766.3:p.Asn1798Asp
ENST00000371375.1:c.4468A>G	ENSP00000360426.1:p.Asn1490Asp
ENST00000371380.7:c.5392A>G	ENSP00000360431.2:p.Asn1798Asp
ENST00000371385.7:c.4468A>G	ENSP00000360438.3:p.Asn1490Asp
NM_001165979.2:c.4468A>G	NP_001159451.1:p.Asn1490Asp
NM_001288989.1:c.5344A>G	NP_001275918.1:p.Asn1782Asp
NM_016341.3:c.5392A>G	NP_057425.3:p.Asn1798Asp
XM_006717885.2:c.5434A>G	XP_006717948.1:p.Asn1812Asp
XM_006717886.2:c.5434A>G	XP_006717949.1:p.Asn1812Asp
XM_006717888.2:c.5431A>G	XP_006717951.1:p.Asn1811Asp
XM_006717889.2:c.5386A>G	XP_006717952.1:p.Asn1796Asp
XM_006717890.1:c.4510A>G	XP_006717953.1:p.Asn1504Asp
XM_011539849.1:c.5434A>G	XP_011538151.1:p.Asn1812Asp
XM_011539850.1:c.4279A>G	XP_011538152.1:p.Asn1427Asp
XM_006717885.4:c.5434A>G	XP_006717948.1:p.Asn1812Asp
XM_006717888.4:c.5431A>G	XP_006717951.1:p.Asn1811Asp
XM_006717889.4:c.5386A>G	XP_006717952.1:p.Asn1796Asp
XM_006717890.3:c.4510A>G	XP_006717953.1:p.Asn1504Asp
XM_011539849.3:c.5434A>G	XP_011538151.1:p.Asn1812Asp
XM_011539850.3:c.4279A>G	XP_011538152.1:p.Asn1427Asp
XM_017016310.2:c.5434A>G	XP_016871799.1:p.Asn1812Asp
XM_017016311.2:c.5434A>G	XP_016871800.1:p.Asn1812Asp
XM_017016312.2:c.4420A>G	XP_016871801.1:p.Asn1474Asp
NM_001288989.2:c.5344A>G	NP_001275918.1:p.Asn1782Asp
NM_016341.4:c.5392A>G MANE Select	NP_057425.3:p.Asn1798Asp