Canonical Allele Identifier: CA116441
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235809351del , CM000663.2:g.235809351del GRCh38
NC_000001.10:g.235972651del , CM000663.1:g.235972651del GRCh37
NC_000001.9:g.234039274del NCBI36
NG_007397.1:g.79290del , LRG_143:g.79290del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697178.1:c.1467del ENSP00000513163.1:p.Glu489AspfsTer?
ENST00000697242.1:c.870del ENSP00000513207.1:p.Glu290AspfsTer?
ENST00000389793.7:c.1467del MANE Select ENSP00000374443.2:p.Glu489AspfsTer?
ENST00000389793.6:c.1467del ENSP00000374443.2:p.Glu489AspfsTer?
ENST00000389794.7:c.1467del ENSP00000374444.4:p.Glu489AspfsTer?
ENST00000465349.5:n.2018del
ENST00000489585.5:n.2018del
NM_000081.3:c.1467del , LRG_143t1:c.1467del NP_000072.2:p.Glu489AspfsTer?
NM_001301365.1:c.1467del , LRG_143t2:c.1467del NP_001288294.1:p.Glu489AspfsTer?
XM_011544031.1:c.1467del XP_011542333.1:p.Glu489AspfsTer?
XM_011544032.1:c.1467del XP_011542334.1:p.Glu489AspfsTer?
XM_011544033.1:c.1467del XP_011542335.1:p.Glu489AspfsTer?
XM_011544034.1:c.1467del XP_011542336.1:p.Glu489AspfsTer?
XM_011544035.1:c.1467del XP_011542337.1:p.Glu489AspfsTer?
XM_011544037.1:c.1467del XP_011542339.1:p.Glu489AspfsTer?
XM_011544038.1:c.1467del XP_011542340.1:p.Glu489AspfsTer?
XM_011544039.1:c.1467del XP_011542341.1:p.Glu489AspfsTer?
XM_011544040.1:c.1467del XP_011542342.1:p.Glu489AspfsTer?
XM_011544033.2:c.1467del XP_011542335.1:p.Glu489AspfsTer?
XM_011544035.2:c.1467del XP_011542337.1:p.Glu489AspfsTer?
XM_011544037.2:c.1467del XP_011542339.1:p.Glu489AspfsTer?
XM_011544039.2:c.1467del XP_011542341.1:p.Glu489AspfsTer?
XM_017000150.1:c.1467del XP_016855639.1:p.Glu489AspfsTer?
XM_017000151.1:c.1467del XP_016855640.1:p.Glu489AspfsTer?
XR_001736946.2:n.1649del
XR_001736947.1:n.1649del
XR_001736948.1:n.1649del
XR_002959252.1:n.1649del
NM_000081.4:c.1467del MANE Select NP_000072.2:p.Glu489AspfsTer?