Canonical Allele Identifier: CA344946949
Gene: LYST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235766112T>G , CM000663.2:g.235766112T>G GRCh38
NC_000001.10:g.235929412T>G , CM000663.1:g.235929412T>G GRCh37
NC_000001.9:g.233996035T>G NCBI36
NG_007397.1:g.122529A>C , LRG_143:g.122529A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000461526.2:c.763A>C ENSP00000513165.1:p.Asn255His
ENST00000697178.1:c.*1512A>C ENSP00000513163.1:n.*1512A>C
ENST00000697180.1:c.593A>C
ENST00000697241.1:c.520A>C ENSP00000513206.1:p.Asn174His
ENST00000389793.7:c.6088A>C MANE Select ENSP00000374443.2:p.Asn2030His
ENST00000389793.6:c.6088A>C ENSP00000374443.2:p.Asn2030His
ENST00000389794.7:c.*1512A>C ENSP00000374444.4:n.*1512A>C
ENST00000489585.5:n.6512+127A>C
NM_000081.3:c.6088A>C , LRG_143t1:c.6088A>C NP_000072.2:p.Asn2030His
NM_001301365.1:c.6088A>C , LRG_143t2:c.6088A>C NP_001288294.1:p.Asn2030His
XM_011544031.1:c.6088A>C XP_011542333.1:p.Asn2030His
XM_011544032.1:c.6088A>C XP_011542334.1:p.Asn2030His
XM_011544033.1:c.6088A>C XP_011542335.1:p.Asn2030His
XM_011544034.1:c.5950A>C XP_011542336.1:p.Asn1984His
XM_011544035.1:c.6088A>C XP_011542337.1:p.Asn2030His
XM_011544036.1:c.3751A>C XP_011542338.1:p.Asn1251His
XM_011544037.1:c.6088A>C XP_011542339.1:p.Asn2030His
XM_011544038.1:c.6088A>C XP_011542340.1:p.Asn2030His
XM_011544039.1:c.6088A>C XP_011542341.1:p.Asn2030His
XM_011544040.1:c.5997A>C XP_011542342.1:p.Thr1999=
XM_011544033.2:c.6088A>C XP_011542335.1:p.Asn2030His
XM_011544035.2:c.6088A>C XP_011542337.1:p.Asn2030His
XM_011544036.2:c.3751A>C XP_011542338.1:p.Asn1251His
XM_011544037.2:c.6088A>C XP_011542339.1:p.Asn2030His
XM_011544039.2:c.6088A>C XP_011542341.1:p.Asn2030His
XM_017000150.1:c.6088A>C XP_016855639.1:p.Asn2030His
XM_017000151.1:c.5859A>C XP_016855640.1:p.Thr1953=
XR_001736946.2:n.6270A>C
XR_001736947.1:n.6270A>C
XR_001736948.1:n.6270A>C
XR_002959252.1:n.6179A>C
NM_000081.4:c.6088A>C MANE Select NP_000072.2:p.Asn2030His