Canonical Allele Identifier: CA1465293
Community Standard Title: NM_000081.4(LYST):c.10758C>T (p.Cys3586=)
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235686991G>A , CM000663.2:g.235686991G>A GRCh38
NC_000001.10:g.235850291G>A , CM000663.1:g.235850291G>A GRCh37
NC_000001.9:g.233916914G>A NCBI36
NG_007397.1:g.201650C>T , LRG_143:g.201650C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000081.4:c.10758C>T MANE Select NP_000072.2:p.Cys3586=
ENST00000389793.7:c.10758C>T MANE Select ENSP00000374443.2:p.Cys3586=
NM_000081.3:c.10758C>T , LRG_143t1:c.10758C>T NP_000072.2:p.Cys3586=
NM_001301365.1:c.10758C>T , LRG_143t2:c.10758C>T NP_001288294.1:p.Cys3586=
ENST00000389793.6:c.10758C>T ENSP00000374443.2:p.Cys3586=
ENST00000389794.7:c.*6182C>T ENSP00000374444.4:n.*6182C>T
ENST00000462376.2:n.2168C>T
ENST00000473037.5:n.5748C>T
ENST00000697178.1:c.*6453C>T ENSP00000513163.1:n.*6453C>T
ENST00000697235.1:c.1308C>T ENSP00000513202.1:p.Cys436=
ENST00000697236.1:c.4222C>T ENSP00000513203.1:n.4222C>T
ENST00000697237.1:c.1469C>T
ENST00000697239.1:n.152C>T
ENST00000697240.1:c.2892C>T ENSP00000513205.1:p.Cys964=
XM_011544031.1:c.10920C>T XP_011542333.1:p.Cys3640=
XM_011544032.1:c.10920C>T XP_011542334.1:p.Cys3640=
XM_011544033.1:c.10920C>T XP_011542335.1:p.Cys3640=
XM_011544033.2:c.10920C>T XP_011542335.1:p.Cys3640=
XM_011544034.1:c.10782C>T XP_011542336.1:p.Cys3594=
XM_011544036.1:c.8583C>T XP_011542338.1:p.Cys2861=
XM_011544036.2:c.8583C>T XP_011542338.1:p.Cys2861=
XM_017000150.1:c.10689C>T XP_016855639.1:p.Cys3563=