Canonical Allele Identifier: CA377641774

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058195A>T (hg19) ; chr10:g.94298438A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298438A>T , CM000672.2:g.94298438A>T	GRCh38
NC_000010.10:g.96058195A>T , CM000672.1:g.96058195A>T	GRCh37
NC_000010.9:g.96048185A>T	NCBI36
NG_015799.1:g.309450A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4303A>T	ENSP00000360426.1:p.Thr1435Ser
ENST00000685253.1:c.*1770A>T	ENSP00000509405.1:n.*1770A>T
ENST00000685889.1:n.1962A>T
ENST00000686807.1:n.646A>T
ENST00000686954.1:c.*511A>T	ENSP00000508416.1:n.*511A>T
ENST00000688810.1:c.4255A>T	ENSP00000509140.1:p.Thr1419Ser
ENST00000689233.1:n.9435A>T
ENST00000690340.1:n.2900A>T
ENST00000692286.1:c.5095A>T	ENSP00000509490.1:p.Thr1699Ser
ENST00000692396.1:c.5179A>T	ENSP00000508605.1:p.Thr1727Ser
ENST00000371380.8:c.5227A>T MANE Select	ENSP00000360431.2:p.Thr1743Ser
ENST00000371385.8:c.4201A>T	ENSP00000360438.4:p.Thr1401Ser
ENST00000674738.1:c.3782A>T
ENST00000674827.1:c.3343A>T	ENSP00000502523.1:p.Thr1115Ser
ENST00000675218.1:c.4303A>T	ENSP00000501910.1:p.Thr1435Ser
ENST00000675487.1:c.*1160A>T	ENSP00000502340.1:n.*1160A>T
ENST00000675718.1:c.4496A>T
ENST00000676102.1:c.4072A>T	ENSP00000502811.1:p.Thr1358Ser
ENST00000260766.7:c.5227A>T	ENSP00000260766.3:p.Thr1743Ser
ENST00000371375.1:c.4303A>T	ENSP00000360426.1:p.Thr1435Ser
ENST00000371380.7:c.5227A>T	ENSP00000360431.2:p.Thr1743Ser
ENST00000371385.7:c.4303A>T	ENSP00000360438.3:p.Thr1435Ser
NM_001165979.2:c.4303A>T	NP_001159451.1:p.Thr1435Ser
NM_001288989.1:c.5179A>T	NP_001275918.1:p.Thr1727Ser
NM_016341.3:c.5227A>T	NP_057425.3:p.Thr1743Ser
XM_006717885.2:c.5269A>T	XP_006717948.1:p.Thr1757Ser
XM_006717886.2:c.5269A>T	XP_006717949.1:p.Thr1757Ser
XM_006717888.2:c.5266A>T	XP_006717951.1:p.Thr1756Ser
XM_006717889.2:c.5221A>T	XP_006717952.1:p.Thr1741Ser
XM_006717890.1:c.4345A>T	XP_006717953.1:p.Thr1449Ser
XM_011539849.1:c.5269A>T	XP_011538151.1:p.Thr1757Ser
XM_011539850.1:c.4114A>T	XP_011538152.1:p.Thr1372Ser
XM_006717885.4:c.5269A>T	XP_006717948.1:p.Thr1757Ser
XM_006717888.4:c.5266A>T	XP_006717951.1:p.Thr1756Ser
XM_006717889.4:c.5221A>T	XP_006717952.1:p.Thr1741Ser
XM_006717890.3:c.4345A>T	XP_006717953.1:p.Thr1449Ser
XM_011539849.3:c.5269A>T	XP_011538151.1:p.Thr1757Ser
XM_011539850.3:c.4114A>T	XP_011538152.1:p.Thr1372Ser
XM_017016310.2:c.5269A>T	XP_016871799.1:p.Thr1757Ser
XM_017016311.2:c.5269A>T	XP_016871800.1:p.Thr1757Ser
XM_017016312.2:c.4255A>T	XP_016871801.1:p.Thr1419Ser
NM_001288989.2:c.5179A>T	NP_001275918.1:p.Thr1727Ser
NM_016341.4:c.5227A>T MANE Select	NP_057425.3:p.Thr1743Ser