Canonical Allele Identifier: CA1466736

Gene: LYST

Linked Data

• ClinVar Variation Id: 254922
• ClinVar RCV Id: RCV000248219 ; RCV001658132 ; RCV002057295
• dbSNP Id: rs150288597
• ExAC: 1:235945406 A / G
• gnomAD v2: 1-235945406-A-G
• gnomAD v3: 1-235782106-A-G
• gnomAD v4: 1-235782106-A-G
• MyVariant Identifiers: chr1:g.235945406A>G (hg19) ; chr1:g.235782106A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235782106A>G , CM000663.2:g.235782106A>G	GRCh38
NC_000001.10:g.235945406A>G , CM000663.1:g.235945406A>G	GRCh37
NC_000001.9:g.234012029A>G	NCBI36
NG_007397.1:g.106535T>C , LRG_143:g.106535T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697178.1:c.*287-19T>C	ENSP00000513163.1:n.*287-19T>C
ENST00000389793.7:c.4863-19T>C MANE Select	ENSP00000374443.2:n.4863-19T>C
ENST00000389793.6:c.4863-19T>C	ENSP00000374443.2:n.4863-19T>C
ENST00000389794.7:c.*287-19T>C	ENSP00000374444.4:n.*287-19T>C
ENST00000489585.5:n.5414-19T>C
NM_000081.3:c.4863-19T>C , LRG_143t1:c.4863-19T>C	NP_000072.2:n.4863-19T>C
NM_001301365.1:c.4863-19T>C , LRG_143t2:c.4863-19T>C	NP_001288294.1:n.4863-19T>C
XM_011544031.1:c.4863-19T>C	XP_011542333.1:n.4863-19T>C
XM_011544032.1:c.4863-19T>C	XP_011542334.1:n.4863-19T>C
XM_011544033.1:c.4863-19T>C	XP_011542335.1:n.4863-19T>C
XM_011544034.1:c.4863-19T>C	XP_011542336.1:n.4863-19T>C
XM_011544035.1:c.4863-19T>C	XP_011542337.1:n.4863-19T>C
XM_011544036.1:c.2526-19T>C	XP_011542338.1:n.2526-19T>C
XM_011544037.1:c.4863-19T>C	XP_011542339.1:n.4863-19T>C
XM_011544038.1:c.4863-19T>C	XP_011542340.1:n.4863-19T>C
XM_011544039.1:c.4863-19T>C	XP_011542341.1:n.4863-19T>C
XM_011544040.1:c.4863-19T>C	XP_011542342.1:n.4863-19T>C
XM_011544033.2:c.4863-19T>C	XP_011542335.1:n.4863-19T>C
XM_011544035.2:c.4863-19T>C	XP_011542337.1:n.4863-19T>C
XM_011544036.2:c.2526-19T>C	XP_011542338.1:n.2526-19T>C
XM_011544037.2:c.4863-19T>C	XP_011542339.1:n.4863-19T>C
XM_011544039.2:c.4863-19T>C	XP_011542341.1:n.4863-19T>C
XM_017000150.1:c.4863-19T>C	XP_016855639.1:n.4863-19T>C
XM_017000151.1:c.4863-19T>C	XP_016855640.1:n.4863-19T>C
XR_001736946.2:n.5045-19T>C
XR_001736947.1:n.5045-19T>C
XR_001736948.1:n.5045-19T>C
XR_002959252.1:n.5045-19T>C
NM_000081.4:c.4863-19T>C MANE Select	NP_000072.2:n.4863-19T>C