Canonical Allele Identifier: CA2739273977

Gene: LYST

Linked Data

• ClinVar Variation Id: 2785056
• ClinVar RCV Id: RCV003636169

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235664072T>C , CM000663.2:g.235664072T>C	GRCh38
NC_000001.10:g.235827372T>C , CM000663.1:g.235827372T>C	GRCh37
NC_000001.9:g.233893995T>C	NCBI36
NG_007397.1:g.224569A>G , LRG_143:g.224569A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462376.2:n.2998A>G
ENST00000697178.1:c.*7182-17A>G	ENSP00000513163.1:n.*7182-17A>G
ENST00000697235.1:c.1746-17A>G	ENSP00000513202.1:n.1746-17A>G
ENST00000697236.1:c.4660-17A>G	ENSP00000513203.1:n.4660-17A>G
ENST00000697237.1:c.1907-17A>G
ENST00000697238.1:n.350-17A>G
ENST00000697239.1:n.590-17A>G
ENST00000697240.1:c.3263-17A>G	ENSP00000513205.1:n.3263-17A>G
ENST00000389793.7:c.11196-17A>G MANE Select	ENSP00000374443.2:n.11196-17A>G
ENST00000389793.6:c.11196-17A>G	ENSP00000374443.2:n.11196-17A>G
ENST00000389794.7:c.*6620-17A>G	ENSP00000374444.4:n.*6620-17A>G
ENST00000473037.5:n.6186-17A>G
NM_000081.3:c.11196-17A>G , LRG_143t1:c.11196-17A>G	NP_000072.2:n.11196-17A>G
NM_001301365.1:c.11196-17A>G , LRG_143t2:c.11196-17A>G	NP_001288294.1:n.11196-17A>G
XM_011544031.1:c.11358-17A>G	XP_011542333.1:n.11358-17A>G
XM_011544032.1:c.11358-17A>G	XP_011542334.1:n.11358-17A>G
XM_011544033.1:c.11358-17A>G	XP_011542335.1:n.11358-17A>G
XM_011544034.1:c.11220-17A>G	XP_011542336.1:n.11220-17A>G
XM_011544036.1:c.9021-17A>G	XP_011542338.1:n.9021-17A>G
XM_011544033.2:c.11358-17A>G	XP_011542335.1:n.11358-17A>G
XM_011544036.2:c.9021-17A>G	XP_011542338.1:n.9021-17A>G
XM_017000150.1:c.11127-17A>G	XP_016855639.1:n.11127-17A>G
NM_000081.4:c.11196-17A>G MANE Select	NP_000072.2:n.11196-17A>G