Canonical Allele Identifier: CA344946970

Gene: LYST

Linked Data

• gnomAD v4: 1-235766115-G-C
• MyVariant Identifiers: chr1:g.235929415G>C (hg19) ; chr1:g.235766115G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235766115G>C , CM000663.2:g.235766115G>C	GRCh38
NC_000001.10:g.235929415G>C , CM000663.1:g.235929415G>C	GRCh37
NC_000001.9:g.233996038G>C	NCBI36
NG_007397.1:g.122526C>G , LRG_143:g.122526C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461526.2:c.760C>G	ENSP00000513165.1:p.His254Asp
ENST00000697178.1:c.*1509C>G	ENSP00000513163.1:n.*1509C>G
ENST00000697180.1:c.590C>G
ENST00000697241.1:c.517C>G	ENSP00000513206.1:p.His173Asp
ENST00000389793.7:c.6085C>G MANE Select	ENSP00000374443.2:p.His2029Asp
ENST00000389793.6:c.6085C>G	ENSP00000374443.2:p.His2029Asp
ENST00000389794.7:c.*1509C>G	ENSP00000374444.4:n.*1509C>G
ENST00000489585.5:n.6512+124C>G
NM_000081.3:c.6085C>G , LRG_143t1:c.6085C>G	NP_000072.2:p.His2029Asp
NM_001301365.1:c.6085C>G , LRG_143t2:c.6085C>G	NP_001288294.1:p.His2029Asp
XM_011544031.1:c.6085C>G	XP_011542333.1:p.His2029Asp
XM_011544032.1:c.6085C>G	XP_011542334.1:p.His2029Asp
XM_011544033.1:c.6085C>G	XP_011542335.1:p.His2029Asp
XM_011544034.1:c.5947C>G	XP_011542336.1:p.His1983Asp
XM_011544035.1:c.6085C>G	XP_011542337.1:p.His2029Asp
XM_011544036.1:c.3748C>G	XP_011542338.1:p.His1250Asp
XM_011544037.1:c.6085C>G	XP_011542339.1:p.His2029Asp
XM_011544038.1:c.6085C>G	XP_011542340.1:p.His2029Asp
XM_011544039.1:c.6085C>G	XP_011542341.1:p.His2029Asp
XM_011544040.1:c.5994C>G	XP_011542342.1:p.Val1998=
XM_011544033.2:c.6085C>G	XP_011542335.1:p.His2029Asp
XM_011544035.2:c.6085C>G	XP_011542337.1:p.His2029Asp
XM_011544036.2:c.3748C>G	XP_011542338.1:p.His1250Asp
XM_011544037.2:c.6085C>G	XP_011542339.1:p.His2029Asp
XM_011544039.2:c.6085C>G	XP_011542341.1:p.His2029Asp
XM_017000150.1:c.6085C>G	XP_016855639.1:p.His2029Asp
XM_017000151.1:c.5856C>G	XP_016855640.1:p.Val1952=
XR_001736946.2:n.6267C>G
XR_001736947.1:n.6267C>G
XR_001736948.1:n.6267C>G
XR_002959252.1:n.6176C>G
NM_000081.4:c.6085C>G MANE Select	NP_000072.2:p.His2029Asp