Canonical Allele Identifier: CA344864
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235777208del , CM000663.2:g.235777208del GRCh38
NC_000001.10:g.235940508del , CM000663.1:g.235940508del GRCh37
NC_000001.9:g.234007131del NCBI36
NG_007397.1:g.111435del , LRG_143:g.111435del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697178.1:c.*741del ENSP00000513163.1:n.*741del
ENST00000389793.7:c.5317del MANE Select ENSP00000374443.2:p.Arg1773AspfsTer13
ENST00000389793.6:c.5317del ENSP00000374443.2:p.Arg1773AspfsTer13
ENST00000389794.7:c.*741del ENSP00000374444.4:n.*741del
ENST00000489585.5:n.5868del
NM_000081.3:c.5317del , LRG_143t1:c.5317del NP_000072.2:p.Arg1773AspfsTer13
NM_001301365.1:c.5317del , LRG_143t2:c.5317del NP_001288294.1:p.Arg1773AspfsTer13
XM_011544031.1:c.5317del XP_011542333.1:p.Arg1773AspfsTer13
XM_011544032.1:c.5317del XP_011542334.1:p.Arg1773AspfsTer13
XM_011544033.1:c.5317del XP_011542335.1:p.Arg1773AspfsTer13
XM_011544034.1:c.5317del XP_011542336.1:p.Arg1773AspfsTer13
XM_011544035.1:c.5317del XP_011542337.1:p.Arg1773AspfsTer13
XM_011544036.1:c.2980del XP_011542338.1:p.Arg994AspfsTer13
XM_011544037.1:c.5317del XP_011542339.1:p.Arg1773AspfsTer13
XM_011544038.1:c.5317del XP_011542340.1:p.Arg1773AspfsTer13
XM_011544039.1:c.5317del XP_011542341.1:p.Arg1773AspfsTer13
XM_011544040.1:c.5317del XP_011542342.1:p.Arg1773AspfsTer13
XM_011544033.2:c.5317del XP_011542335.1:p.Arg1773AspfsTer13
XM_011544035.2:c.5317del XP_011542337.1:p.Arg1773AspfsTer13
XM_011544036.2:c.2980del XP_011542338.1:p.Arg994AspfsTer13
XM_011544037.2:c.5317del XP_011542339.1:p.Arg1773AspfsTer13
XM_011544039.2:c.5317del XP_011542341.1:p.Arg1773AspfsTer13
XM_017000150.1:c.5317del XP_016855639.1:p.Arg1773AspfsTer13
XM_017000151.1:c.5317del XP_016855640.1:p.Arg1773AspfsTer13
XR_001736946.2:n.5499del
XR_001736947.1:n.5499del
XR_001736948.1:n.5499del
XR_002959252.1:n.5499del
NM_000081.4:c.5317del MANE Select NP_000072.2:p.Arg1773AspfsTer13