Canonical Allele Identifier: CA39626258

Gene: LYST

Linked Data

• dbSNP Id: rs547984434
• gnomAD v2: 1-236039834-A-G
• gnomAD v3: 1-235876534-A-G
• gnomAD v4: 1-235876534-A-G
• MyVariant Identifiers: chr1:g.236039834A>G (hg19) ; chr1:g.235876534A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235876534A>G , CM000663.2:g.235876534A>G	GRCh38
NC_000001.10:g.236039834A>G , CM000663.1:g.236039834A>G	GRCh37
NC_000001.9:g.234106457A>G	NCBI36
NG_007397.1:g.12107T>C , LRG_143:g.12107T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697178.1:c.-98+6653T>C	ENSP00000513163.1:n.-98+6653T>C
ENST00000697181.1:c.-98+6653T>C	ENSP00000513168.1:n.-98+6653T>C
ENST00000697182.1:c.-98+6653T>C	ENSP00000513169.1:n.-98+6653T>C
ENST00000697185.1:n.475-3505T>C
ENST00000697186.1:n.527-3509T>C
ENST00000697248.1:n.528-3505T>C
ENST00000697249.1:n.215-3509T>C
ENST00000465349.5:n.454+6653T>C
ENST00000468107.5:n.430+6653T>C
ENST00000489585.5:n.454+6653T>C
NM_001301365.1:c.-98+6653T>C , LRG_143t2:c.-98+6653T>C	NP_001288294.1:n.-98+6653T>C
NR_102436.2:n.522+6653T>C
XM_011544032.1:c.-98+6653T>C	XP_011542334.1:n.-98+6653T>C
NR_102436.3:n.527+6653T>C