Canonical Allele Identifier: CA344946906
Gene: LYST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235766106T>A , CM000663.2:g.235766106T>A GRCh38
NC_000001.10:g.235929406T>A , CM000663.1:g.235929406T>A GRCh37
NC_000001.9:g.233996029T>A NCBI36
NG_007397.1:g.122535A>T , LRG_143:g.122535A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000461526.2:c.769A>T ENSP00000513165.1:p.Thr257Ser
ENST00000697178.1:c.*1518A>T ENSP00000513163.1:n.*1518A>T
ENST00000697180.1:c.599A>T
ENST00000697241.1:c.526A>T ENSP00000513206.1:p.Thr176Ser
ENST00000389793.7:c.6094A>T MANE Select ENSP00000374443.2:p.Thr2032Ser
ENST00000389793.6:c.6094A>T ENSP00000374443.2:p.Thr2032Ser
ENST00000389794.7:c.*1518A>T ENSP00000374444.4:n.*1518A>T
ENST00000489585.5:n.6512+133A>T
NM_000081.3:c.6094A>T , LRG_143t1:c.6094A>T NP_000072.2:p.Thr2032Ser
NM_001301365.1:c.6094A>T , LRG_143t2:c.6094A>T NP_001288294.1:p.Thr2032Ser
XM_011544031.1:c.6094A>T XP_011542333.1:p.Thr2032Ser
XM_011544032.1:c.6094A>T XP_011542334.1:p.Thr2032Ser
XM_011544033.1:c.6094A>T XP_011542335.1:p.Thr2032Ser
XM_011544034.1:c.5956A>T XP_011542336.1:p.Thr1986Ser
XM_011544035.1:c.6094A>T XP_011542337.1:p.Thr2032Ser
XM_011544036.1:c.3757A>T XP_011542338.1:p.Thr1253Ser
XM_011544037.1:c.6094A>T XP_011542339.1:p.Thr2032Ser
XM_011544038.1:c.6094A>T XP_011542340.1:p.Thr2032Ser
XM_011544039.1:c.6094A>T XP_011542341.1:p.Thr2032Ser
XM_011544040.1:c.6003A>T XP_011542342.1:p.Pro2001=
XM_011544033.2:c.6094A>T XP_011542335.1:p.Thr2032Ser
XM_011544035.2:c.6094A>T XP_011542337.1:p.Thr2032Ser
XM_011544036.2:c.3757A>T XP_011542338.1:p.Thr1253Ser
XM_011544037.2:c.6094A>T XP_011542339.1:p.Thr2032Ser
XM_011544039.2:c.6094A>T XP_011542341.1:p.Thr2032Ser
XM_017000150.1:c.6094A>T XP_016855639.1:p.Thr2032Ser
XM_017000151.1:c.5865A>T XP_016855640.1:p.Pro1955=
XR_001736946.2:n.6276A>T
XR_001736947.1:n.6276A>T
XR_001736948.1:n.6276A>T
XR_002959252.1:n.6185A>T
NM_000081.4:c.6094A>T MANE Select NP_000072.2:p.Thr2032Ser