Canonical Allele Identifier: CA2486634988
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235766214T= , CM000663.2:g.235766214T= GRCh38
NC_000001.10:g.235929514T= , CM000663.1:g.235929514T= GRCh37
NC_000001.9:g.233996137T= NCBI36
NG_007397.1:g.122427A= , LRG_143:g.122427A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461526.2:c.661A= ENSP00000513165.1:p.Ile221=
ENST00000697178.1:c.*1410A= ENSP00000513163.1:n.*1410A=
ENST00000697180.1:c.557+25A=
ENST00000697241.1:c.418A= ENSP00000513206.1:p.Ile140=
ENST00000389793.7:c.5986A= MANE Select ENSP00000374443.2:p.Ile1996=
ENST00000389793.6:c.5986A= ENSP00000374443.2:p.Ile1996=
ENST00000389794.7:c.*1410A= ENSP00000374444.4:n.*1410A=
ENST00000489585.5:n.6512+25A=
NM_000081.3:c.5986A= , LRG_143t1:c.5986A= NP_000072.2:p.Ile1996=
NM_001301365.1:c.5986A= , LRG_143t2:c.5986A= NP_001288294.1:p.Ile1996=
XM_011544031.1:c.5986A= XP_011542333.1:p.Ile1996=
XM_011544032.1:c.5986A= XP_011542334.1:p.Ile1996=
XM_011544033.1:c.5986A= XP_011542335.1:p.Ile1996=
XM_011544034.1:c.5848A= XP_011542336.1:p.Ile1950=
XM_011544035.1:c.5986A= XP_011542337.1:p.Ile1996=
XM_011544036.1:c.3649A= XP_011542338.1:p.Ile1217=
XM_011544037.1:c.5986A= XP_011542339.1:p.Ile1996=
XM_011544038.1:c.5986A= XP_011542340.1:p.Ile1996=
XM_011544039.1:c.5986A= XP_011542341.1:p.Ile1996=
XM_011544040.1:c.5961+25A= XP_011542342.1:n.5961+25A=
XM_011544033.2:c.5986A= XP_011542335.1:p.Ile1996=
XM_011544035.2:c.5986A= XP_011542337.1:p.Ile1996=
XM_011544036.2:c.3649A= XP_011542338.1:p.Ile1217=
XM_011544037.2:c.5986A= XP_011542339.1:p.Ile1996=
XM_011544039.2:c.5986A= XP_011542341.1:p.Ile1996=
XM_017000150.1:c.5986A= XP_016855639.1:p.Ile1996=
XM_017000151.1:c.5823+25A= XP_016855640.1:n.5823+25A=
XR_001736946.2:n.6168A=
XR_001736947.1:n.6168A=
XR_001736948.1:n.6168A=
XR_002959252.1:n.6143+25A=
NM_000081.4:c.5986A= MANE Select NP_000072.2:p.Ile1996=