Canonical Allele Identifier: CA1929002225
Community Standard Title: NM_016341.4(PLCE1):c.5885-391A=
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94308190A= , CM000672.2:g.94308190A= GRCh38
NC_000010.10:g.96067947A= , CM000672.1:g.96067947A= GRCh37
NC_000010.9:g.96057937A= NCBI36
NG_015799.1:g.319202A=

Transcript Alleles

HGVS Amino-acid Change
NM_016341.4:c.5885-391A= MANE Select NP_057425.3:n.5885-391A=
ENST00000371380.8:c.5885-391A= MANE Select ENSP00000360431.2:n.5885-391A=
NM_001165979.2:c.4961-391A= NP_001159451.1:n.4961-391A=
NM_001288989.1:c.5837-391A= NP_001275918.1:n.5837-391A=
NM_001288989.2:c.5837-391A= NP_001275918.1:n.5837-391A=
NM_016341.3:c.5885-391A= NP_057425.3:n.5885-391A=
ENST00000260766.7:c.5885-391A= ENSP00000260766.3:n.5885-391A=
ENST00000371375.1:c.4961-391A= ENSP00000360426.1:n.4961-391A=
ENST00000371375.2:c.4961-391A= ENSP00000360426.1:n.4961-391A=
ENST00000371380.7:c.5885-391A= ENSP00000360431.2:n.5885-391A=
ENST00000371385.7:c.4961-391A= ENSP00000360438.3:n.4961-391A=
ENST00000371385.8:c.4859-391A= ENSP00000360438.4:n.4859-391A=
ENST00000674738.1:c.4440-391A=
ENST00000674827.1:c.4001-391A= ENSP00000502523.1:n.4001-391A=
ENST00000675218.1:c.4961-391A= ENSP00000501910.1:n.4961-391A=
ENST00000675487.1:c.*1818-391A= ENSP00000502340.1:n.*1818-391A=
ENST00000675718.1:c.5154-391A=
ENST00000685253.1:c.*2428-391A= ENSP00000509405.1:n.*2428-391A=
ENST00000685889.1:n.2620-391A=
ENST00000686807.1:n.1304-391A=
ENST00000686954.1:c.*1169-391A= ENSP00000508416.1:n.*1169-391A=
ENST00000688810.1:c.4913-391A= ENSP00000509140.1:n.4913-391A=
ENST00000689233.1:n.10093-391A=
ENST00000690340.1:n.3558-391A=
ENST00000692286.1:c.5753-391A= ENSP00000509490.1:n.5753-391A=
ENST00000692396.1:c.5837-391A= ENSP00000508605.1:n.5837-391A=
XM_006717885.2:c.5927-391A= XP_006717948.1:n.5927-391A=
XM_006717885.4:c.5927-391A= XP_006717948.1:n.5927-391A=
XM_006717886.2:c.5927-391A= XP_006717949.1:n.5927-391A=
XM_006717888.2:c.5924-391A= XP_006717951.1:n.5924-391A=
XM_006717888.4:c.5924-391A= XP_006717951.1:n.5924-391A=
XM_006717889.2:c.5879-391A= XP_006717952.1:n.5879-391A=
XM_006717889.4:c.5879-391A= XP_006717952.1:n.5879-391A=
XM_006717890.1:c.5003-391A= XP_006717953.1:n.5003-391A=
XM_006717890.3:c.5003-391A= XP_006717953.1:n.5003-391A=
XM_011539849.1:c.5927-391A= XP_011538151.1:n.5927-391A=
XM_011539849.3:c.5927-391A= XP_011538151.1:n.5927-391A=
XM_011539850.1:c.4772-391A= XP_011538152.1:n.4772-391A=
XM_011539850.3:c.4772-391A= XP_011538152.1:n.4772-391A=
XM_017016310.2:c.5927-391A= XP_016871799.1:n.5927-391A=
XM_017016311.2:c.5927-391A= XP_016871800.1:n.5927-391A=
XM_017016312.2:c.4913-391A= XP_016871801.1:n.4913-391A=