Canonical Allele Identifier: CA377640564

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053304A>C (hg19) ; chr10:g.94293547A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293547A>C , CM000672.2:g.94293547A>C	GRCh38
NC_000010.10:g.96053304A>C , CM000672.1:g.96053304A>C	GRCh37
NC_000010.9:g.96043294A>C	NCBI36
NG_015799.1:g.304559A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4151A>C	ENSP00000360426.1:p.Lys1384Thr
ENST00000685253.1:c.*1618A>C	ENSP00000509405.1:n.*1618A>C
ENST00000685889.1:n.1810A>C
ENST00000686807.1:n.494A>C
ENST00000686954.1:c.*359A>C	ENSP00000508416.1:n.*359A>C
ENST00000688810.1:c.4103A>C	ENSP00000509140.1:p.Lys1368Thr
ENST00000689233.1:n.9283A>C
ENST00000690340.1:n.2748A>C
ENST00000692286.1:c.5036-4832A>C	ENSP00000509490.1:n.5036-4832A>C
ENST00000692396.1:c.5027A>C	ENSP00000508605.1:p.Lys1676Thr
ENST00000371380.8:c.5075A>C MANE Select	ENSP00000360431.2:p.Lys1692Thr
ENST00000371385.8:c.4049A>C	ENSP00000360438.4:p.Lys1350Thr
ENST00000674738.1:c.3630A>C
ENST00000674827.1:c.3191A>C	ENSP00000502523.1:p.Lys1064Thr
ENST00000675218.1:c.4151A>C	ENSP00000501910.1:p.Lys1384Thr
ENST00000675487.1:c.*1008A>C	ENSP00000502340.1:n.*1008A>C
ENST00000675718.1:c.4344A>C
ENST00000676102.1:c.3920A>C	ENSP00000502811.1:p.Lys1307Thr
ENST00000260766.7:c.5075A>C	ENSP00000260766.3:p.Lys1692Thr
ENST00000371375.1:c.4151A>C	ENSP00000360426.1:p.Lys1384Thr
ENST00000371380.7:c.5075A>C	ENSP00000360431.2:p.Lys1692Thr
ENST00000371385.7:c.4151A>C	ENSP00000360438.3:p.Lys1384Thr
NM_001165979.2:c.4151A>C	NP_001159451.1:p.Lys1384Thr
NM_001288989.1:c.5027A>C	NP_001275918.1:p.Lys1676Thr
NM_016341.3:c.5075A>C	NP_057425.3:p.Lys1692Thr
XM_006717885.2:c.5117A>C	XP_006717948.1:p.Lys1706Thr
XM_006717886.2:c.5117A>C	XP_006717949.1:p.Lys1706Thr
XM_006717888.2:c.5114A>C	XP_006717951.1:p.Lys1705Thr
XM_006717889.2:c.5069A>C	XP_006717952.1:p.Lys1690Thr
XM_006717890.1:c.4193A>C	XP_006717953.1:p.Lys1398Thr
XM_011539849.1:c.5117A>C	XP_011538151.1:p.Lys1706Thr
XM_011539850.1:c.3962A>C	XP_011538152.1:p.Lys1321Thr
XM_006717885.4:c.5117A>C	XP_006717948.1:p.Lys1706Thr
XM_006717888.4:c.5114A>C	XP_006717951.1:p.Lys1705Thr
XM_006717889.4:c.5069A>C	XP_006717952.1:p.Lys1690Thr
XM_006717890.3:c.4193A>C	XP_006717953.1:p.Lys1398Thr
XM_011539849.3:c.5117A>C	XP_011538151.1:p.Lys1706Thr
XM_011539850.3:c.3962A>C	XP_011538152.1:p.Lys1321Thr
XM_017016310.2:c.5117A>C	XP_016871799.1:p.Lys1706Thr
XM_017016311.2:c.5117A>C	XP_016871800.1:p.Lys1706Thr
XM_017016312.2:c.4103A>C	XP_016871801.1:p.Lys1368Thr
NM_001288989.2:c.5027A>C	NP_001275918.1:p.Lys1676Thr
NM_016341.4:c.5075A>C MANE Select	NP_057425.3:p.Lys1692Thr