Canonical Allele Identifier: CA377642004
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298544A>G , CM000672.2:g.94298544A>G GRCh38
NC_000010.10:g.96058301A>G , CM000672.1:g.96058301A>G GRCh37
NC_000010.9:g.96048291A>G NCBI36
NG_015799.1:g.309556A>G

Transcript Alleles

HGVS Amino-acid change
NM_001165979.2:c.4409A>G NP_001159451.1:p.Gln1470Arg
NM_001288989.1:c.5285A>G NP_001275918.1:p.Gln1762Arg
NM_016341.3:c.5333A>G NP_057425.3:p.Gln1778Arg
XM_006717885.2:c.5375A>G XP_006717948.1:p.Gln1792Arg
XM_006717886.2:c.5375A>G XP_006717949.1:p.Gln1792Arg
XM_006717888.2:c.5372A>G XP_006717951.1:p.Gln1791Arg
XM_006717889.2:c.5327A>G XP_006717952.1:p.Gln1776Arg
XM_006717890.1:c.4451A>G XP_006717953.1:p.Gln1484Arg
XM_011539849.1:c.5375A>G XP_011538151.1:p.Gln1792Arg
XM_011539850.1:c.4220A>G XP_011538152.1:p.Gln1407Arg
XM_006717885.4:c.5375A>G XP_006717948.1:p.Gln1792Arg
XM_006717888.4:c.5372A>G XP_006717951.1:p.Gln1791Arg
XM_006717889.4:c.5327A>G XP_006717952.1:p.Gln1776Arg
XM_006717890.3:c.4451A>G XP_006717953.1:p.Gln1484Arg
XM_011539849.3:c.5375A>G XP_011538151.1:p.Gln1792Arg
XM_011539850.3:c.4220A>G XP_011538152.1:p.Gln1407Arg
XM_017016310.2:c.5375A>G XP_016871799.1:p.Gln1792Arg
XM_017016311.2:c.5375A>G XP_016871800.1:p.Gln1792Arg
XM_017016312.2:c.4361A>G XP_016871801.1:p.Gln1454Arg
NM_001288989.2:c.5285A>G NP_001275918.1:p.Gln1762Arg
NM_016341.4:c.5333A>G MANE Select NP_057425.3:p.Gln1778Arg
ENST00000260766.7:c.5333A>G ENSP00000260766.3:p.Gln1778Arg
ENST00000371375.1:n.4409A>G ENSP00000360426.1:p.Gln1470Arg
ENST00000371380.7:c.5333A>G ENSP00000360431.2:p.Gln1778Arg
ENST00000371385.7:c.4409A>G ENSP00000360438.3:p.Gln1470Arg