Canonical Allele Identifier: CA2486632357
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235759338T= , CM000663.2:g.235759338T= GRCh38
NC_000001.10:g.235922638T= , CM000663.1:g.235922638T= GRCh37
NC_000001.9:g.233989261T= NCBI36
NG_007397.1:g.129303A= , LRG_143:g.129303A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461526.2:c.1190A= ENSP00000513165.1:p.Lys397=
ENST00000697178.1:c.*1939A= ENSP00000513163.1:n.*1939A=
ENST00000697236.1:c.224A= ENSP00000513203.1:p.Lys75=
ENST00000697241.1:c.947A= ENSP00000513206.1:p.Lys316=
ENST00000389793.7:c.6515A= MANE Select ENSP00000374443.2:p.Lys2172=
ENST00000389793.6:c.6515A= ENSP00000374443.2:p.Lys2172=
ENST00000389794.7:c.*1939A= ENSP00000374444.4:n.*1939A=
ENST00000489585.5:n.6906A=
NM_000081.3:c.6515A= , LRG_143t1:c.6515A= NP_000072.2:p.Lys2172=
NM_001301365.1:c.6515A= , LRG_143t2:c.6515A= NP_001288294.1:p.Lys2172=
XM_011544031.1:c.6515A= XP_011542333.1:p.Lys2172=
XM_011544032.1:c.6515A= XP_011542334.1:p.Lys2172=
XM_011544033.1:c.6515A= XP_011542335.1:p.Lys2172=
XM_011544034.1:c.6377A= XP_011542336.1:p.Lys2126=
XM_011544035.1:c.6515A= XP_011542337.1:p.Lys2172=
XM_011544036.1:c.4178A= XP_011542338.1:p.Lys1393=
XM_011544037.1:c.6515A= XP_011542339.1:p.Lys2172=
XM_011544038.1:c.6515A= XP_011542340.1:p.Lys2172=
XM_011544039.1:c.6515A= XP_011542341.1:p.Lys2172=
XM_011544033.2:c.6515A= XP_011542335.1:p.Lys2172=
XM_011544035.2:c.6515A= XP_011542337.1:p.Lys2172=
XM_011544036.2:c.4178A= XP_011542338.1:p.Lys1393=
XM_011544037.2:c.6515A= XP_011542339.1:p.Lys2172=
XM_011544039.2:c.6515A= XP_011542341.1:p.Lys2172=
XM_017000150.1:c.6515A= XP_016855639.1:p.Lys2172=
XR_001736946.2:n.6697A=
XR_001736947.1:n.6697A=
XR_001736948.1:n.6697A=
NM_000081.4:c.6515A= MANE Select NP_000072.2:p.Lys2172=