Canonical Allele Identifier: CA733149208

Gene: LYST

Linked Data

• dbSNP Id: rs1294532733
• MyVariant Identifiers: chr1:g.236039950C>T (hg19) ; chr1:g.235876650C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235876650C>T , CM000663.2:g.235876650C>T	GRCh38
NC_000001.10:g.236039950C>T , CM000663.1:g.236039950C>T	GRCh37
NC_000001.9:g.234106573C>T	NCBI36
NG_007397.1:g.11991G>A , LRG_143:g.11991G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697178.1:c.-98+6537G>A	ENSP00000513163.1:n.-98+6537G>A
ENST00000697181.1:c.-98+6537G>A	ENSP00000513168.1:n.-98+6537G>A
ENST00000697182.1:c.-98+6537G>A	ENSP00000513169.1:n.-98+6537G>A
ENST00000697185.1:n.475-3621G>A
ENST00000697186.1:n.527-3625G>A
ENST00000697248.1:n.528-3621G>A
ENST00000697249.1:n.215-3625G>A
ENST00000465349.5:n.454+6537G>A
ENST00000468107.5:n.430+6537G>A
ENST00000489585.5:n.454+6537G>A
NM_001301365.1:c.-98+6537G>A , LRG_143t2:c.-98+6537G>A	NP_001288294.1:n.-98+6537G>A
NR_102436.2:n.522+6537G>A
XM_011544032.1:c.-98+6537G>A	XP_011542334.1:n.-98+6537G>A
NR_102436.3:n.527+6537G>A