Canonical Allele Identifier: CA377641893

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058250A>C (hg19) ; chr10:g.94298493A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298493A>C , CM000672.2:g.94298493A>C	GRCh38
NC_000010.10:g.96058250A>C , CM000672.1:g.96058250A>C	GRCh37
NC_000010.9:g.96048240A>C	NCBI36
NG_015799.1:g.309505A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4358A>C	ENSP00000360426.1:p.Asn1453Thr
ENST00000685253.1:c.*1825A>C	ENSP00000509405.1:n.*1825A>C
ENST00000685889.1:n.2017A>C
ENST00000686807.1:n.701A>C
ENST00000686954.1:c.*566A>C	ENSP00000508416.1:n.*566A>C
ENST00000688810.1:c.4310A>C	ENSP00000509140.1:p.Asn1437Thr
ENST00000689233.1:n.9490A>C
ENST00000690340.1:n.2955A>C
ENST00000692286.1:c.5150A>C	ENSP00000509490.1:p.Asn1717Thr
ENST00000692396.1:c.5234A>C	ENSP00000508605.1:p.Asn1745Thr
ENST00000371380.8:c.5282A>C MANE Select	ENSP00000360431.2:p.Asn1761Thr
ENST00000371385.8:c.4256A>C	ENSP00000360438.4:p.Asn1419Thr
ENST00000674738.1:c.3837A>C
ENST00000674827.1:c.3398A>C	ENSP00000502523.1:p.Asn1133Thr
ENST00000675218.1:c.4358A>C	ENSP00000501910.1:p.Asn1453Thr
ENST00000675487.1:c.*1215A>C	ENSP00000502340.1:n.*1215A>C
ENST00000675718.1:c.4551A>C
ENST00000260766.7:c.5282A>C	ENSP00000260766.3:p.Asn1761Thr
ENST00000371375.1:c.4358A>C	ENSP00000360426.1:p.Asn1453Thr
ENST00000371380.7:c.5282A>C	ENSP00000360431.2:p.Asn1761Thr
ENST00000371385.7:c.4358A>C	ENSP00000360438.3:p.Asn1453Thr
NM_001165979.2:c.4358A>C	NP_001159451.1:p.Asn1453Thr
NM_001288989.1:c.5234A>C	NP_001275918.1:p.Asn1745Thr
NM_016341.3:c.5282A>C	NP_057425.3:p.Asn1761Thr
XM_006717885.2:c.5324A>C	XP_006717948.1:p.Asn1775Thr
XM_006717886.2:c.5324A>C	XP_006717949.1:p.Asn1775Thr
XM_006717888.2:c.5321A>C	XP_006717951.1:p.Asn1774Thr
XM_006717889.2:c.5276A>C	XP_006717952.1:p.Asn1759Thr
XM_006717890.1:c.4400A>C	XP_006717953.1:p.Asn1467Thr
XM_011539849.1:c.5324A>C	XP_011538151.1:p.Asn1775Thr
XM_011539850.1:c.4169A>C	XP_011538152.1:p.Asn1390Thr
XM_006717885.4:c.5324A>C	XP_006717948.1:p.Asn1775Thr
XM_006717888.4:c.5321A>C	XP_006717951.1:p.Asn1774Thr
XM_006717889.4:c.5276A>C	XP_006717952.1:p.Asn1759Thr
XM_006717890.3:c.4400A>C	XP_006717953.1:p.Asn1467Thr
XM_011539849.3:c.5324A>C	XP_011538151.1:p.Asn1775Thr
XM_011539850.3:c.4169A>C	XP_011538152.1:p.Asn1390Thr
XM_017016310.2:c.5324A>C	XP_016871799.1:p.Asn1775Thr
XM_017016311.2:c.5324A>C	XP_016871800.1:p.Asn1775Thr
XM_017016312.2:c.4310A>C	XP_016871801.1:p.Asn1437Thr
NM_001288989.2:c.5234A>C	NP_001275918.1:p.Asn1745Thr
NM_016341.4:c.5282A>C MANE Select	NP_057425.3:p.Asn1761Thr