Canonical Allele Identifier: CA931349689

Gene: PLCE1 PLCE1-AS1

Linked Data

• dbSNP Id: rs2052126777

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94279782del , CM000672.2:g.94279782del	GRCh38
NC_000010.10:g.96039539del , CM000672.1:g.96039539del	GRCh37
NC_000010.9:g.96029529del	NCBI36
NG_015799.1:g.290794del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.3742del (PLCE1)
ENST00000685253.1:c.*1209del (PLCE1)
ENST00000685889.1:n.1401del (PLCE1)
ENST00000686954.1:c.4666del (PLCE1)
ENST00000688810.1:c.3694del (PLCE1)
ENST00000689233.1:n.4996del (PLCE1)
ENST00000692286.1:c.4666del (PLCE1)
ENST00000692396.1:c.4618del (PLCE1)
ENST00000371380.8:c.4666del (PLCE1)
ENST00000371385.8:c.3640del (PLCE1)
ENST00000674738.1:c.3071del (PLCE1)
ENST00000674827.1:c.2743del (PLCE1)
ENST00000675218.1:c.3742del (PLCE1)
ENST00000675487.1:c.*599del (PLCE1)
ENST00000675718.1:c.3893del (PLCE1)
ENST00000676102.1:c.3511del (PLCE1)
ENST00000260766.7:c.4666del (PLCE1)
ENST00000371375.1:c.3742del (PLCE1)
ENST00000371380.7:c.4666del (PLCE1)
ENST00000371385.7:c.3742del (PLCE1)
NM_001165979.2:c.3742del (PLCE1)
NM_001288989.1:c.4618del (PLCE1)
NM_016341.3:c.4666del (PLCE1)
NR_033969.1:n.917del (PLCE1-AS1)
XM_006717885.2:c.4666del (PLCE1)
XM_006717886.2:c.4666del (PLCE1)
XM_006717888.2:c.4666del (PLCE1)
XM_006717889.2:c.4618del (PLCE1)
XM_006717890.1:c.3742del (PLCE1)
XM_011539849.1:c.4666del (PLCE1)
XM_011539850.1:c.3511del (PLCE1)
XM_011539851.1:c.4666del (PLCE1)
XM_011539852.1:c.4666del (PLCE1)
XM_006717885.4:c.4666del (PLCE1)
XM_006717888.4:c.4666del (PLCE1)
XM_006717889.4:c.4618del (PLCE1)
XM_006717890.3:c.3742del (PLCE1)
XM_011539849.3:c.4666del (PLCE1)
XM_011539850.3:c.3511del (PLCE1)
XM_011539851.3:c.4666del (PLCE1)
XM_011539852.3:c.4666del (PLCE1)
XM_017016310.2:c.4666del (PLCE1)
XM_017016311.2:c.4666del (PLCE1)
XM_017016312.2:c.3694del (PLCE1)
NM_001288989.2:c.4618del (PLCE1)
NM_016341.4:c.4666del (PLCE1)