Canonical Allele Identifier: CA377641832

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058222C>T (hg19) ; chr10:g.94298465C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298465C>T , CM000672.2:g.94298465C>T	GRCh38
NC_000010.10:g.96058222C>T , CM000672.1:g.96058222C>T	GRCh37
NC_000010.9:g.96048212C>T	NCBI36
NG_015799.1:g.309477C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4330C>T	ENSP00000360426.1:p.Pro1444Ser
ENST00000685253.1:c.*1797C>T	ENSP00000509405.1:n.*1797C>T
ENST00000685889.1:n.1989C>T
ENST00000686807.1:n.673C>T
ENST00000686954.1:c.*538C>T	ENSP00000508416.1:n.*538C>T
ENST00000688810.1:c.4282C>T	ENSP00000509140.1:p.Pro1428Ser
ENST00000689233.1:n.9462C>T
ENST00000690340.1:n.2927C>T
ENST00000692286.1:c.5122C>T	ENSP00000509490.1:p.Pro1708Ser
ENST00000692396.1:c.5206C>T	ENSP00000508605.1:p.Pro1736Ser
ENST00000371380.8:c.5254C>T MANE Select	ENSP00000360431.2:p.Pro1752Ser
ENST00000371385.8:c.4228C>T	ENSP00000360438.4:p.Pro1410Ser
ENST00000674738.1:c.3809C>T
ENST00000674827.1:c.3370C>T	ENSP00000502523.1:p.Pro1124Ser
ENST00000675218.1:c.4330C>T	ENSP00000501910.1:p.Pro1444Ser
ENST00000675487.1:c.*1187C>T	ENSP00000502340.1:n.*1187C>T
ENST00000675718.1:c.4523C>T
ENST00000676102.1:c.4099C>T	ENSP00000502811.1:p.Pro1367Ser
ENST00000260766.7:c.5254C>T	ENSP00000260766.3:p.Pro1752Ser
ENST00000371375.1:c.4330C>T	ENSP00000360426.1:p.Pro1444Ser
ENST00000371380.7:c.5254C>T	ENSP00000360431.2:p.Pro1752Ser
ENST00000371385.7:c.4330C>T	ENSP00000360438.3:p.Pro1444Ser
NM_001165979.2:c.4330C>T	NP_001159451.1:p.Pro1444Ser
NM_001288989.1:c.5206C>T	NP_001275918.1:p.Pro1736Ser
NM_016341.3:c.5254C>T	NP_057425.3:p.Pro1752Ser
XM_006717885.2:c.5296C>T	XP_006717948.1:p.Pro1766Ser
XM_006717886.2:c.5296C>T	XP_006717949.1:p.Pro1766Ser
XM_006717888.2:c.5293C>T	XP_006717951.1:p.Pro1765Ser
XM_006717889.2:c.5248C>T	XP_006717952.1:p.Pro1750Ser
XM_006717890.1:c.4372C>T	XP_006717953.1:p.Pro1458Ser
XM_011539849.1:c.5296C>T	XP_011538151.1:p.Pro1766Ser
XM_011539850.1:c.4141C>T	XP_011538152.1:p.Pro1381Ser
XM_006717885.4:c.5296C>T	XP_006717948.1:p.Pro1766Ser
XM_006717888.4:c.5293C>T	XP_006717951.1:p.Pro1765Ser
XM_006717889.4:c.5248C>T	XP_006717952.1:p.Pro1750Ser
XM_006717890.3:c.4372C>T	XP_006717953.1:p.Pro1458Ser
XM_011539849.3:c.5296C>T	XP_011538151.1:p.Pro1766Ser
XM_011539850.3:c.4141C>T	XP_011538152.1:p.Pro1381Ser
XM_017016310.2:c.5296C>T	XP_016871799.1:p.Pro1766Ser
XM_017016311.2:c.5296C>T	XP_016871800.1:p.Pro1766Ser
XM_017016312.2:c.4282C>T	XP_016871801.1:p.Pro1428Ser
NM_001288989.2:c.5206C>T	NP_001275918.1:p.Pro1736Ser
NM_016341.4:c.5254C>T MANE Select	NP_057425.3:p.Pro1752Ser