Canonical Allele Identifier: CA377642324

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058412A>C (hg19) ; chr10:g.94298655A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298655A>C , CM000672.2:g.94298655A>C	GRCh38
NC_000010.10:g.96058412A>C , CM000672.1:g.96058412A>C	GRCh37
NC_000010.9:g.96048402A>C	NCBI36
NG_015799.1:g.309667A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4520A>C	ENSP00000360426.1:p.Asn1507Thr
ENST00000685253.1:c.*1987A>C	ENSP00000509405.1:n.*1987A>C
ENST00000685889.1:n.2179A>C
ENST00000686807.1:n.863A>C
ENST00000686954.1:c.*728A>C	ENSP00000508416.1:n.*728A>C
ENST00000688810.1:c.4472A>C	ENSP00000509140.1:p.Asn1491Thr
ENST00000689233.1:n.9652A>C
ENST00000690340.1:n.3117A>C
ENST00000692286.1:c.5312A>C	ENSP00000509490.1:p.Asn1771Thr
ENST00000692396.1:c.5396A>C	ENSP00000508605.1:p.Asn1799Thr
ENST00000371380.8:c.5444A>C MANE Select	ENSP00000360431.2:p.Asn1815Thr
ENST00000371385.8:c.4418A>C	ENSP00000360438.4:p.Asn1473Thr
ENST00000674738.1:c.3999A>C
ENST00000674827.1:c.3560A>C	ENSP00000502523.1:p.Asn1187Thr
ENST00000675218.1:c.4520A>C	ENSP00000501910.1:p.Asn1507Thr
ENST00000675487.1:c.*1377A>C	ENSP00000502340.1:n.*1377A>C
ENST00000675718.1:c.4713A>C
ENST00000260766.7:c.5444A>C	ENSP00000260766.3:p.Asn1815Thr
ENST00000371375.1:c.4520A>C	ENSP00000360426.1:p.Asn1507Thr
ENST00000371380.7:c.5444A>C	ENSP00000360431.2:p.Asn1815Thr
ENST00000371385.7:c.4520A>C	ENSP00000360438.3:p.Asn1507Thr
NM_001165979.2:c.4520A>C	NP_001159451.1:p.Asn1507Thr
NM_001288989.1:c.5396A>C	NP_001275918.1:p.Asn1799Thr
NM_016341.3:c.5444A>C	NP_057425.3:p.Asn1815Thr
XM_006717885.2:c.5486A>C	XP_006717948.1:p.Asn1829Thr
XM_006717886.2:c.5486A>C	XP_006717949.1:p.Asn1829Thr
XM_006717888.2:c.5483A>C	XP_006717951.1:p.Asn1828Thr
XM_006717889.2:c.5438A>C	XP_006717952.1:p.Asn1813Thr
XM_006717890.1:c.4562A>C	XP_006717953.1:p.Asn1521Thr
XM_011539849.1:c.5486A>C	XP_011538151.1:p.Asn1829Thr
XM_011539850.1:c.4331A>C	XP_011538152.1:p.Asn1444Thr
XM_006717885.4:c.5486A>C	XP_006717948.1:p.Asn1829Thr
XM_006717888.4:c.5483A>C	XP_006717951.1:p.Asn1828Thr
XM_006717889.4:c.5438A>C	XP_006717952.1:p.Asn1813Thr
XM_006717890.3:c.4562A>C	XP_006717953.1:p.Asn1521Thr
XM_011539849.3:c.5486A>C	XP_011538151.1:p.Asn1829Thr
XM_011539850.3:c.4331A>C	XP_011538152.1:p.Asn1444Thr
XM_017016310.2:c.5486A>C	XP_016871799.1:p.Asn1829Thr
XM_017016311.2:c.5486A>C	XP_016871800.1:p.Asn1829Thr
XM_017016312.2:c.4472A>C	XP_016871801.1:p.Asn1491Thr
NM_001288989.2:c.5396A>C	NP_001275918.1:p.Asn1799Thr
NM_016341.4:c.5444A>C MANE Select	NP_057425.3:p.Asn1815Thr