Canonical Allele Identifier: CA344987039
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235664583C>G , CM000663.2:g.235664583C>G GRCh38
NC_000001.10:g.235827883C>G , CM000663.1:g.235827883C>G GRCh37
NC_000001.9:g.233894506C>G NCBI36
NG_007397.1:g.224058G>C , LRG_143:g.224058G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000462376.2:n.2487G>C
ENST00000697178.1:c.*7063G>C ENSP00000513163.1:n.*7063G>C
ENST00000697235.1:c.1627G>C ENSP00000513202.1:p.Gly543Arg
ENST00000697236.1:c.4541G>C ENSP00000513203.1:n.4541G>C
ENST00000697237.1:c.1788G>C
ENST00000697238.1:n.231G>C
ENST00000697239.1:n.471G>C
ENST00000697240.1:c.3173-29G>C ENSP00000513205.1:n.3173-29G>C
ENST00000389793.7:c.11077G>C MANE Select ENSP00000374443.2:p.Gly3693Arg
ENST00000389793.6:c.11077G>C ENSP00000374443.2:p.Gly3693Arg
ENST00000389794.7:c.*6501G>C ENSP00000374444.4:n.*6501G>C
ENST00000473037.5:n.6067G>C
NM_000081.3:c.11077G>C , LRG_143t1:c.11077G>C NP_000072.2:p.Gly3693Arg
NM_001301365.1:c.11077G>C , LRG_143t2:c.11077G>C NP_001288294.1:p.Gly3693Arg
XM_011544031.1:c.11239G>C XP_011542333.1:p.Gly3747Arg
XM_011544032.1:c.11239G>C XP_011542334.1:p.Gly3747Arg
XM_011544033.1:c.11239G>C XP_011542335.1:p.Gly3747Arg
XM_011544034.1:c.11101G>C XP_011542336.1:p.Gly3701Arg
XM_011544036.1:c.8902G>C XP_011542338.1:p.Gly2968Arg
XM_011544033.2:c.11239G>C XP_011542335.1:p.Gly3747Arg
XM_011544036.2:c.8902G>C XP_011542338.1:p.Gly2968Arg
XM_017000150.1:c.11008G>C XP_016855639.1:p.Gly3670Arg
NM_000081.4:c.11077G>C MANE Select NP_000072.2:p.Gly3693Arg