Canonical Allele Identifier: CA377640904

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053378A>C (hg19) ; chr10:g.94293621A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293621A>C , CM000672.2:g.94293621A>C	GRCh38
NC_000010.10:g.96053378A>C , CM000672.1:g.96053378A>C	GRCh37
NC_000010.9:g.96043368A>C	NCBI36
NG_015799.1:g.304633A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4225A>C	ENSP00000360426.1:p.Asn1409His
ENST00000685253.1:c.*1692A>C	ENSP00000509405.1:n.*1692A>C
ENST00000685889.1:n.1884A>C
ENST00000686807.1:n.568A>C
ENST00000686954.1:c.*433A>C	ENSP00000508416.1:n.*433A>C
ENST00000688810.1:c.4177A>C	ENSP00000509140.1:p.Asn1393His
ENST00000689233.1:n.9357A>C
ENST00000690340.1:n.2822A>C
ENST00000692286.1:c.5036-4758A>C	ENSP00000509490.1:n.5036-4758A>C
ENST00000692396.1:c.5101A>C	ENSP00000508605.1:p.Asn1701His
ENST00000371380.8:c.5149A>C MANE Select	ENSP00000360431.2:p.Asn1717His
ENST00000371385.8:c.4123A>C	ENSP00000360438.4:p.Asn1375His
ENST00000674738.1:c.3704A>C
ENST00000674827.1:c.3265A>C	ENSP00000502523.1:p.Asn1089His
ENST00000675218.1:c.4225A>C	ENSP00000501910.1:p.Asn1409His
ENST00000675487.1:c.*1082A>C	ENSP00000502340.1:n.*1082A>C
ENST00000675718.1:c.4418A>C
ENST00000676102.1:c.3994A>C	ENSP00000502811.1:p.Asn1332His
ENST00000260766.7:c.5149A>C	ENSP00000260766.3:p.Asn1717His
ENST00000371375.1:c.4225A>C	ENSP00000360426.1:p.Asn1409His
ENST00000371380.7:c.5149A>C	ENSP00000360431.2:p.Asn1717His
ENST00000371385.7:c.4225A>C	ENSP00000360438.3:p.Asn1409His
NM_001165979.2:c.4225A>C	NP_001159451.1:p.Asn1409His
NM_001288989.1:c.5101A>C	NP_001275918.1:p.Asn1701His
NM_016341.3:c.5149A>C	NP_057425.3:p.Asn1717His
XM_006717885.2:c.5191A>C	XP_006717948.1:p.Asn1731His
XM_006717886.2:c.5191A>C	XP_006717949.1:p.Asn1731His
XM_006717888.2:c.5188A>C	XP_006717951.1:p.Asn1730His
XM_006717889.2:c.5143A>C	XP_006717952.1:p.Asn1715His
XM_006717890.1:c.4267A>C	XP_006717953.1:p.Asn1423His
XM_011539849.1:c.5191A>C	XP_011538151.1:p.Asn1731His
XM_011539850.1:c.4036A>C	XP_011538152.1:p.Asn1346His
XM_006717885.4:c.5191A>C	XP_006717948.1:p.Asn1731His
XM_006717888.4:c.5188A>C	XP_006717951.1:p.Asn1730His
XM_006717889.4:c.5143A>C	XP_006717952.1:p.Asn1715His
XM_006717890.3:c.4267A>C	XP_006717953.1:p.Asn1423His
XM_011539849.3:c.5191A>C	XP_011538151.1:p.Asn1731His
XM_011539850.3:c.4036A>C	XP_011538152.1:p.Asn1346His
XM_017016310.2:c.5191A>C	XP_016871799.1:p.Asn1731His
XM_017016311.2:c.5191A>C	XP_016871800.1:p.Asn1731His
XM_017016312.2:c.4177A>C	XP_016871801.1:p.Asn1393His
NM_001288989.2:c.5101A>C	NP_001275918.1:p.Asn1701His
NM_016341.4:c.5149A>C MANE Select	NP_057425.3:p.Asn1717His