Canonical Allele Identifier: CA2698358165
Gene: LYST HGNC NCBI

Linked Data

dbSNP Id: rs2103237761

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235876610T>C , CM000663.2:g.235876610T>C GRCh38
NC_000001.10:g.236039910T>C , CM000663.1:g.236039910T>C GRCh37
NC_000001.9:g.234106533T>C NCBI36
NG_007397.1:g.12031A>G , LRG_143:g.12031A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697178.1:c.-98+6577A>G ENSP00000513163.1:n.-98+6577A>G
ENST00000697181.1:c.-98+6577A>G ENSP00000513168.1:n.-98+6577A>G
ENST00000697182.1:c.-98+6577A>G ENSP00000513169.1:n.-98+6577A>G
ENST00000697185.1:n.475-3581A>G
ENST00000697186.1:n.527-3585A>G
ENST00000697248.1:n.528-3581A>G
ENST00000697249.1:n.215-3585A>G
ENST00000465349.5:n.454+6577A>G
ENST00000468107.5:n.430+6577A>G
ENST00000489585.5:n.454+6577A>G
NM_001301365.1:c.-98+6577A>G , LRG_143t2:c.-98+6577A>G NP_001288294.1:n.-98+6577A>G
NR_102436.2:n.522+6577A>G
XM_011544032.1:c.-98+6577A>G XP_011542334.1:n.-98+6577A>G
NR_102436.3:n.527+6577A>G