Canonical Allele Identifier: CA733149113

Gene: LYST

Linked Data

• dbSNP Id: rs1263999403
• gnomAD v3: 1-235876414-G-A
• gnomAD v4: 1-235876414-G-A
• MyVariant Identifiers: chr1:g.236039714G>A (hg19) ; chr1:g.235876414G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235876414G>A , CM000663.2:g.235876414G>A	GRCh38
NC_000001.10:g.236039714G>A , CM000663.1:g.236039714G>A	GRCh37
NC_000001.9:g.234106337G>A	NCBI36
NG_007397.1:g.12227C>T , LRG_143:g.12227C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697178.1:c.-98+6773C>T	ENSP00000513163.1:n.-98+6773C>T
ENST00000697181.1:c.-98+6773C>T	ENSP00000513168.1:n.-98+6773C>T
ENST00000697182.1:c.-98+6773C>T	ENSP00000513169.1:n.-98+6773C>T
ENST00000697185.1:n.475-3385C>T
ENST00000697186.1:n.527-3389C>T
ENST00000697248.1:n.528-3385C>T
ENST00000697249.1:n.215-3389C>T
ENST00000465349.5:n.454+6773C>T
ENST00000468107.5:n.430+6773C>T
ENST00000489585.5:n.454+6773C>T
NM_001301365.1:c.-98+6773C>T , LRG_143t2:c.-98+6773C>T	NP_001288294.1:n.-98+6773C>T
NR_102436.2:n.522+6773C>T
XM_011544032.1:c.-98+6773C>T	XP_011542334.1:n.-98+6773C>T
NR_102436.3:n.527+6773C>T