Canonical Allele Identifier: CA39626232

Gene: LYST

Linked Data

• dbSNP Id: rs954539996
• gnomAD v2: 1-236039743-A-C
• gnomAD v3: 1-235876443-A-C
• gnomAD v4: 1-235876443-A-C
• MyVariant Identifiers: chr1:g.236039743A>C (hg19) ; chr1:g.235876443A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235876443A>C , CM000663.2:g.235876443A>C	GRCh38
NC_000001.10:g.236039743A>C , CM000663.1:g.236039743A>C	GRCh37
NC_000001.9:g.234106366A>C	NCBI36
NG_007397.1:g.12198T>G , LRG_143:g.12198T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697178.1:c.-98+6744T>G	ENSP00000513163.1:n.-98+6744T>G
ENST00000697181.1:c.-98+6744T>G	ENSP00000513168.1:n.-98+6744T>G
ENST00000697182.1:c.-98+6744T>G	ENSP00000513169.1:n.-98+6744T>G
ENST00000697185.1:n.475-3414T>G
ENST00000697186.1:n.527-3418T>G
ENST00000697248.1:n.528-3414T>G
ENST00000697249.1:n.215-3418T>G
ENST00000465349.5:n.454+6744T>G
ENST00000468107.5:n.430+6744T>G
ENST00000489585.5:n.454+6744T>G
NM_001301365.1:c.-98+6744T>G , LRG_143t2:c.-98+6744T>G	NP_001288294.1:n.-98+6744T>G
NR_102436.2:n.522+6744T>G
XM_011544032.1:c.-98+6744T>G	XP_011542334.1:n.-98+6744T>G
NR_102436.3:n.527+6744T>G