Canonical Allele Identifier: CA344946931
Gene: LYST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235766109G>C , CM000663.2:g.235766109G>C GRCh38
NC_000001.10:g.235929409G>C , CM000663.1:g.235929409G>C GRCh37
NC_000001.9:g.233996032G>C NCBI36
NG_007397.1:g.122532C>G , LRG_143:g.122532C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000461526.2:c.766C>G ENSP00000513165.1:p.Pro256Ala
ENST00000697178.1:c.*1515C>G ENSP00000513163.1:n.*1515C>G
ENST00000697180.1:c.596C>G
ENST00000697241.1:c.523C>G ENSP00000513206.1:p.Pro175Ala
ENST00000389793.7:c.6091C>G MANE Select ENSP00000374443.2:p.Pro2031Ala
ENST00000389793.6:c.6091C>G ENSP00000374443.2:p.Pro2031Ala
ENST00000389794.7:c.*1515C>G ENSP00000374444.4:n.*1515C>G
ENST00000489585.5:n.6512+130C>G
NM_000081.3:c.6091C>G , LRG_143t1:c.6091C>G NP_000072.2:p.Pro2031Ala
NM_001301365.1:c.6091C>G , LRG_143t2:c.6091C>G NP_001288294.1:p.Pro2031Ala
XM_011544031.1:c.6091C>G XP_011542333.1:p.Pro2031Ala
XM_011544032.1:c.6091C>G XP_011542334.1:p.Pro2031Ala
XM_011544033.1:c.6091C>G XP_011542335.1:p.Pro2031Ala
XM_011544034.1:c.5953C>G XP_011542336.1:p.Pro1985Ala
XM_011544035.1:c.6091C>G XP_011542337.1:p.Pro2031Ala
XM_011544036.1:c.3754C>G XP_011542338.1:p.Pro1252Ala
XM_011544037.1:c.6091C>G XP_011542339.1:p.Pro2031Ala
XM_011544038.1:c.6091C>G XP_011542340.1:p.Pro2031Ala
XM_011544039.1:c.6091C>G XP_011542341.1:p.Pro2031Ala
XM_011544040.1:c.6000C>G XP_011542342.1:p.Ile2000Met
XM_011544033.2:c.6091C>G XP_011542335.1:p.Pro2031Ala
XM_011544035.2:c.6091C>G XP_011542337.1:p.Pro2031Ala
XM_011544036.2:c.3754C>G XP_011542338.1:p.Pro1252Ala
XM_011544037.2:c.6091C>G XP_011542339.1:p.Pro2031Ala
XM_011544039.2:c.6091C>G XP_011542341.1:p.Pro2031Ala
XM_017000150.1:c.6091C>G XP_016855639.1:p.Pro2031Ala
XM_017000151.1:c.5862C>G XP_016855640.1:p.Ile1954Met
XR_001736946.2:n.6273C>G
XR_001736947.1:n.6273C>G
XR_001736948.1:n.6273C>G
XR_002959252.1:n.6182C>G
NM_000081.4:c.6091C>G MANE Select NP_000072.2:p.Pro2031Ala