Canonical Allele Identifier: CA646721282
Gene: LYST HGNC NCBI

Linked Data

dbSNP Id: rs1681145567

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235876558A>G , CM000663.2:g.235876558A>G GRCh38
NC_000001.10:g.236039858A>G , CM000663.1:g.236039858A>G GRCh37
NC_000001.9:g.234106481A>G NCBI36
NG_007397.1:g.12083T>C , LRG_143:g.12083T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697178.1:c.-98+6629T>C ENSP00000513163.1:n.-98+6629T>C
ENST00000697181.1:c.-98+6629T>C ENSP00000513168.1:n.-98+6629T>C
ENST00000697182.1:c.-98+6629T>C ENSP00000513169.1:n.-98+6629T>C
ENST00000697185.1:n.475-3529T>C
ENST00000697186.1:n.527-3533T>C
ENST00000697248.1:n.528-3529T>C
ENST00000697249.1:n.215-3533T>C
ENST00000465349.5:n.454+6629T>C
ENST00000468107.5:n.430+6629T>C
ENST00000489585.5:n.454+6629T>C
NM_001301365.1:c.-98+6629T>C , LRG_143t2:c.-98+6629T>C NP_001288294.1:n.-98+6629T>C
NR_102436.2:n.522+6629T>C
XM_011544032.1:c.-98+6629T>C XP_011542334.1:n.-98+6629T>C
NR_102436.3:n.527+6629T>C