Canonical Allele Identifier: CA2486626464
Community Standard Title: NM_000081.4(LYST):c.7982C= (p.Ser2661=)
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235744148G= , CM000663.2:g.235744148G= GRCh38
NC_000001.10:g.235907448G= , CM000663.1:g.235907448G= GRCh37
NC_000001.9:g.233974071G= NCBI36
NG_007397.1:g.144493C= , LRG_143:g.144493C=

Transcript Alleles

HGVS Amino-acid Change
NM_000081.4:c.7982C= MANE Select NP_000072.2:p.Ser2661=
ENST00000389793.7:c.7982C= MANE Select ENSP00000374443.2:p.Ser2661=
NM_000081.3:c.7982C= , LRG_143t1:c.7982C= NP_000072.2:p.Ser2661=
NM_001301365.1:c.7982C= , LRG_143t2:c.7982C= NP_001288294.1:p.Ser2661=
ENST00000389793.6:c.7982C= ENSP00000374443.2:p.Ser2661=
ENST00000389794.7:c.*3406C= ENSP00000374444.4:n.*3406C=
ENST00000461526.2:c.2657C= ENSP00000513165.1:p.Ser886=
ENST00000475277.2:c.77C= ENSP00000513164.1:p.Ser26=
ENST00000697178.1:c.*3406C= ENSP00000513163.1:n.*3406C=
ENST00000697236.1:c.1691C= ENSP00000513203.1:p.Ser564=
ENST00000697240.1:c.116C= ENSP00000513205.1:p.Ser39=
ENST00000697241.1:c.2462C= ENSP00000513206.1:p.Ser821=
XM_011544031.1:c.8144C= XP_011542333.1:p.Ser2715=
XM_011544032.1:c.8144C= XP_011542334.1:p.Ser2715=
XM_011544033.1:c.8144C= XP_011542335.1:p.Ser2715=
XM_011544033.2:c.8144C= XP_011542335.1:p.Ser2715=
XM_011544034.1:c.8006C= XP_011542336.1:p.Ser2669=
XM_011544035.1:c.8144C= XP_011542337.1:p.Ser2715=
XM_011544035.2:c.8144C= XP_011542337.1:p.Ser2715=
XM_011544036.1:c.5807C= XP_011542338.1:p.Ser1936=
XM_011544036.2:c.5807C= XP_011542338.1:p.Ser1936=
XM_011544037.1:c.8144C= XP_011542339.1:p.Ser2715=
XM_011544037.2:c.8144C= XP_011542339.1:p.Ser2715=
XM_011544038.1:c.8144C= XP_011542340.1:p.Ser2715=
XM_017000150.1:c.8144C= XP_016855639.1:p.Ser2715=
XR_001736946.2:n.8326C=
XR_001736947.1:n.8164C=
XR_001736948.1:n.7613C=