Canonical Allele Identifier: CA423772783
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235741572A>G , CM000663.2:g.235741572A>G GRCh38
NC_000001.10:g.235904872A>G , CM000663.1:g.235904872A>G GRCh37
NC_000001.9:g.233971495A>G NCBI36
NG_007397.1:g.147069T>C , LRG_143:g.147069T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000461526.2:c.2883T>C ENSP00000513165.1:p.Cys961=
ENST00000475277.2:c.303T>C ENSP00000513164.1:p.Cys101=
ENST00000697178.1:c.*3632T>C ENSP00000513163.1:n.*3632T>C
ENST00000697236.1:c.1917T>C ENSP00000513203.1:p.Cys639=
ENST00000697240.1:c.342T>C ENSP00000513205.1:p.Cys114=
ENST00000697241.1:c.2688T>C ENSP00000513206.1:p.Cys896=
ENST00000389793.7:c.8208T>C MANE Select ENSP00000374443.2:p.Cys2736=
ENST00000389793.6:c.8208T>C ENSP00000374443.2:p.Cys2736=
ENST00000389794.7:c.*3632T>C ENSP00000374444.4:n.*3632T>C
ENST00000461526.1:n.111T>C
NM_000081.3:c.8208T>C , LRG_143t1:c.8208T>C NP_000072.2:p.Cys2736=
NM_001301365.1:c.8208T>C , LRG_143t2:c.8208T>C NP_001288294.1:p.Cys2736=
XM_011544031.1:c.8370T>C XP_011542333.1:p.Cys2790=
XM_011544032.1:c.8370T>C XP_011542334.1:p.Cys2790=
XM_011544033.1:c.8370T>C XP_011542335.1:p.Cys2790=
XM_011544034.1:c.8232T>C XP_011542336.1:p.Cys2744=
XM_011544035.1:c.8370T>C XP_011542337.1:p.Cys2790=
XM_011544036.1:c.6033T>C XP_011542338.1:p.Cys2011=
XM_011544037.1:c.8370T>C XP_011542339.1:p.Cys2790=
XM_011544038.1:c.8370T>C XP_011542340.1:p.Cys2790=
XM_011544033.2:c.8370T>C XP_011542335.1:p.Cys2790=
XM_011544035.2:c.8370T>C XP_011542337.1:p.Cys2790=
XM_011544036.2:c.6033T>C XP_011542338.1:p.Cys2011=
XM_011544037.2:c.8370T>C XP_011542339.1:p.Cys2790=
XM_017000150.1:c.8370T>C XP_016855639.1:p.Cys2790=
XR_001736946.2:n.8552T>C
XR_001736947.1:n.8390T>C
XR_001736948.1:n.7839T>C
NM_000081.4:c.8208T>C MANE Select NP_000072.2:p.Cys2736=