Canonical Allele Identifier: CA344986870
Community Standard Title: NM_000081.4(LYST):c.11116T>A (p.Cys3706Ser)
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235664544A>T , CM000663.2:g.235664544A>T GRCh38
NC_000001.10:g.235827844A>T , CM000663.1:g.235827844A>T GRCh37
NC_000001.9:g.233894467A>T NCBI36
NG_007397.1:g.224097T>A , LRG_143:g.224097T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000081.4:c.11116T>A MANE Select NP_000072.2:p.Cys3706Ser
ENST00000389793.7:c.11116T>A MANE Select ENSP00000374443.2:p.Cys3706Ser
NM_000081.3:c.11116T>A , LRG_143t1:c.11116T>A NP_000072.2:p.Cys3706Ser
NM_001301365.1:c.11116T>A , LRG_143t2:c.11116T>A NP_001288294.1:p.Cys3706Ser
ENST00000389793.6:c.11116T>A ENSP00000374443.2:p.Cys3706Ser
ENST00000389794.7:c.*6540T>A ENSP00000374444.4:n.*6540T>A
ENST00000462376.2:n.2526T>A
ENST00000473037.5:n.6106T>A
ENST00000697178.1:c.*7102T>A ENSP00000513163.1:n.*7102T>A
ENST00000697235.1:c.1666T>A ENSP00000513202.1:p.Cys556Ser
ENST00000697236.1:c.4580T>A ENSP00000513203.1:n.4580T>A
ENST00000697237.1:c.1827T>A
ENST00000697238.1:n.270T>A
ENST00000697239.1:n.510T>A
ENST00000697240.1:c.3183T>A ENSP00000513205.1:p.Ser1061=
XM_011544031.1:c.11278T>A XP_011542333.1:p.Cys3760Ser
XM_011544032.1:c.11278T>A XP_011542334.1:p.Cys3760Ser
XM_011544033.1:c.11278T>A XP_011542335.1:p.Cys3760Ser
XM_011544033.2:c.11278T>A XP_011542335.1:p.Cys3760Ser
XM_011544034.1:c.11140T>A XP_011542336.1:p.Cys3714Ser
XM_011544036.1:c.8941T>A XP_011542338.1:p.Cys2981Ser
XM_011544036.2:c.8941T>A XP_011542338.1:p.Cys2981Ser
XM_017000150.1:c.11047T>A XP_016855639.1:p.Cys3683Ser