Canonical Allele Identifier: CA2698358152
Gene: LYST HGNC NCBI

Linked Data

dbSNP Id: rs2103237345

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235876439C>A , CM000663.2:g.235876439C>A GRCh38
NC_000001.10:g.236039739C>A , CM000663.1:g.236039739C>A GRCh37
NC_000001.9:g.234106362C>A NCBI36
NG_007397.1:g.12202G>T , LRG_143:g.12202G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697178.1:c.-98+6748G>T ENSP00000513163.1:n.-98+6748G>T
ENST00000697181.1:c.-98+6748G>T ENSP00000513168.1:n.-98+6748G>T
ENST00000697182.1:c.-98+6748G>T ENSP00000513169.1:n.-98+6748G>T
ENST00000697185.1:n.475-3410G>T
ENST00000697186.1:n.527-3414G>T
ENST00000697248.1:n.528-3410G>T
ENST00000697249.1:n.215-3414G>T
ENST00000465349.5:n.454+6748G>T
ENST00000468107.5:n.430+6748G>T
ENST00000489585.5:n.454+6748G>T
NM_001301365.1:c.-98+6748G>T , LRG_143t2:c.-98+6748G>T NP_001288294.1:n.-98+6748G>T
NR_102436.2:n.522+6748G>T
XM_011544032.1:c.-98+6748G>T XP_011542334.1:n.-98+6748G>T
NR_102436.3:n.527+6748G>T