Canonical Allele Identifier: CA2486677508
Gene: LYST HGNC NCBI

Linked Data

dbSNP Id: rs1681147346

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235876587dup , CM000663.2:g.235876587dup GRCh38
NC_000001.10:g.236039887dup , CM000663.1:g.236039887dup GRCh37
NC_000001.9:g.234106510dup NCBI36
NG_007397.1:g.12057dup , LRG_143:g.12057dup

Transcript Alleles

HGVS Amino-acid change
ENST00000697178.1:c.-98+6603dup ENSP00000513163.1:n.-98+6603dup
ENST00000697181.1:c.-98+6603dup ENSP00000513168.1:n.-98+6603dup
ENST00000697182.1:c.-98+6603dup ENSP00000513169.1:n.-98+6603dup
ENST00000697185.1:n.475-3555dup
ENST00000697186.1:n.527-3559dup
ENST00000697248.1:n.528-3555dup
ENST00000697249.1:n.215-3559dup
ENST00000465349.5:n.454+6603dup
ENST00000468107.5:n.430+6603dup
ENST00000489585.5:n.454+6603dup
NM_001301365.1:c.-98+6603dup , LRG_143t2:c.-98+6603dup NP_001288294.1:n.-98+6603dup
NR_102436.2:n.522+6603dup
XM_011544032.1:c.-98+6603dup XP_011542334.1:n.-98+6603dup
NR_102436.3:n.527+6603dup