Canonical Allele Identifier: CA377642386

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058424A>T (hg19) ; chr10:g.94298667A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298667A>T , CM000672.2:g.94298667A>T	GRCh38
NC_000010.10:g.96058424A>T , CM000672.1:g.96058424A>T	GRCh37
NC_000010.9:g.96048414A>T	NCBI36
NG_015799.1:g.309679A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4532A>T	ENSP00000360426.1:p.Asp1511Val
ENST00000685253.1:c.*1999A>T	ENSP00000509405.1:n.*1999A>T
ENST00000685889.1:n.2191A>T
ENST00000686807.1:n.875A>T
ENST00000686954.1:c.*740A>T	ENSP00000508416.1:n.*740A>T
ENST00000688810.1:c.4484A>T	ENSP00000509140.1:p.Asp1495Val
ENST00000689233.1:n.9664A>T
ENST00000690340.1:n.3129A>T
ENST00000692286.1:c.5324A>T	ENSP00000509490.1:p.Asp1775Val
ENST00000692396.1:c.5408A>T	ENSP00000508605.1:p.Asp1803Val
ENST00000371380.8:c.5456A>T MANE Select	ENSP00000360431.2:p.Asp1819Val
ENST00000371385.8:c.4430A>T	ENSP00000360438.4:p.Asp1477Val
ENST00000674738.1:c.4011A>T
ENST00000674827.1:c.3572A>T	ENSP00000502523.1:p.Asp1191Val
ENST00000675218.1:c.4532A>T	ENSP00000501910.1:p.Asp1511Val
ENST00000675487.1:c.*1389A>T	ENSP00000502340.1:n.*1389A>T
ENST00000675718.1:c.4725A>T
ENST00000260766.7:c.5456A>T	ENSP00000260766.3:p.Asp1819Val
ENST00000371375.1:c.4532A>T	ENSP00000360426.1:p.Asp1511Val
ENST00000371380.7:c.5456A>T	ENSP00000360431.2:p.Asp1819Val
ENST00000371385.7:c.4532A>T	ENSP00000360438.3:p.Asp1511Val
NM_001165979.2:c.4532A>T	NP_001159451.1:p.Asp1511Val
NM_001288989.1:c.5408A>T	NP_001275918.1:p.Asp1803Val
NM_016341.3:c.5456A>T	NP_057425.3:p.Asp1819Val
XM_006717885.2:c.5498A>T	XP_006717948.1:p.Asp1833Val
XM_006717886.2:c.5498A>T	XP_006717949.1:p.Asp1833Val
XM_006717888.2:c.5495A>T	XP_006717951.1:p.Asp1832Val
XM_006717889.2:c.5450A>T	XP_006717952.1:p.Asp1817Val
XM_006717890.1:c.4574A>T	XP_006717953.1:p.Asp1525Val
XM_011539849.1:c.5498A>T	XP_011538151.1:p.Asp1833Val
XM_011539850.1:c.4343A>T	XP_011538152.1:p.Asp1448Val
XM_006717885.4:c.5498A>T	XP_006717948.1:p.Asp1833Val
XM_006717888.4:c.5495A>T	XP_006717951.1:p.Asp1832Val
XM_006717889.4:c.5450A>T	XP_006717952.1:p.Asp1817Val
XM_006717890.3:c.4574A>T	XP_006717953.1:p.Asp1525Val
XM_011539849.3:c.5498A>T	XP_011538151.1:p.Asp1833Val
XM_011539850.3:c.4343A>T	XP_011538152.1:p.Asp1448Val
XM_017016310.2:c.5498A>T	XP_016871799.1:p.Asp1833Val
XM_017016311.2:c.5498A>T	XP_016871800.1:p.Asp1833Val
XM_017016312.2:c.4484A>T	XP_016871801.1:p.Asp1495Val
NM_001288989.2:c.5408A>T	NP_001275918.1:p.Asp1803Val
NM_016341.4:c.5456A>T MANE Select	NP_057425.3:p.Asp1819Val