Canonical Allele Identifier: CA377641763

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058189C>T (hg19) ; chr10:g.94298432C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298432C>T , CM000672.2:g.94298432C>T	GRCh38
NC_000010.10:g.96058189C>T , CM000672.1:g.96058189C>T	GRCh37
NC_000010.9:g.96048179C>T	NCBI36
NG_015799.1:g.309444C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4297C>T	ENSP00000360426.1:p.Pro1433Ser
ENST00000685253.1:c.*1764C>T	ENSP00000509405.1:n.*1764C>T
ENST00000685889.1:n.1956C>T
ENST00000686807.1:n.640C>T
ENST00000686954.1:c.*505C>T	ENSP00000508416.1:n.*505C>T
ENST00000688810.1:c.4249C>T	ENSP00000509140.1:p.Pro1417Ser
ENST00000689233.1:n.9429C>T
ENST00000690340.1:n.2894C>T
ENST00000692286.1:c.5089C>T	ENSP00000509490.1:p.Pro1697Ser
ENST00000692396.1:c.5173C>T	ENSP00000508605.1:p.Pro1725Ser
ENST00000371380.8:c.5221C>T MANE Select	ENSP00000360431.2:p.Pro1741Ser
ENST00000371385.8:c.4195C>T	ENSP00000360438.4:p.Pro1399Ser
ENST00000674738.1:c.3776C>T
ENST00000674827.1:c.3337C>T	ENSP00000502523.1:p.Pro1113Ser
ENST00000675218.1:c.4297C>T	ENSP00000501910.1:p.Pro1433Ser
ENST00000675487.1:c.*1154C>T	ENSP00000502340.1:n.*1154C>T
ENST00000675718.1:c.4490C>T
ENST00000676102.1:c.4066C>T	ENSP00000502811.1:p.Pro1356Ser
ENST00000260766.7:c.5221C>T	ENSP00000260766.3:p.Pro1741Ser
ENST00000371375.1:c.4297C>T	ENSP00000360426.1:p.Pro1433Ser
ENST00000371380.7:c.5221C>T	ENSP00000360431.2:p.Pro1741Ser
ENST00000371385.7:c.4297C>T	ENSP00000360438.3:p.Pro1433Ser
NM_001165979.2:c.4297C>T	NP_001159451.1:p.Pro1433Ser
NM_001288989.1:c.5173C>T	NP_001275918.1:p.Pro1725Ser
NM_016341.3:c.5221C>T	NP_057425.3:p.Pro1741Ser
XM_006717885.2:c.5263C>T	XP_006717948.1:p.Pro1755Ser
XM_006717886.2:c.5263C>T	XP_006717949.1:p.Pro1755Ser
XM_006717888.2:c.5260C>T	XP_006717951.1:p.Pro1754Ser
XM_006717889.2:c.5215C>T	XP_006717952.1:p.Pro1739Ser
XM_006717890.1:c.4339C>T	XP_006717953.1:p.Pro1447Ser
XM_011539849.1:c.5263C>T	XP_011538151.1:p.Pro1755Ser
XM_011539850.1:c.4108C>T	XP_011538152.1:p.Pro1370Ser
XM_006717885.4:c.5263C>T	XP_006717948.1:p.Pro1755Ser
XM_006717888.4:c.5260C>T	XP_006717951.1:p.Pro1754Ser
XM_006717889.4:c.5215C>T	XP_006717952.1:p.Pro1739Ser
XM_006717890.3:c.4339C>T	XP_006717953.1:p.Pro1447Ser
XM_011539849.3:c.5263C>T	XP_011538151.1:p.Pro1755Ser
XM_011539850.3:c.4108C>T	XP_011538152.1:p.Pro1370Ser
XM_017016310.2:c.5263C>T	XP_016871799.1:p.Pro1755Ser
XM_017016311.2:c.5263C>T	XP_016871800.1:p.Pro1755Ser
XM_017016312.2:c.4249C>T	XP_016871801.1:p.Pro1417Ser
NM_001288989.2:c.5173C>T	NP_001275918.1:p.Pro1725Ser
NM_016341.4:c.5221C>T MANE Select	NP_057425.3:p.Pro1741Ser