Canonical Allele Identifier: CA344946952

Gene: LYST

Linked Data

• MyVariant Identifiers: chr1:g.235929413G>C (hg19) ; chr1:g.235766113G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235766113G>C , CM000663.2:g.235766113G>C	GRCh38
NC_000001.10:g.235929413G>C , CM000663.1:g.235929413G>C	GRCh37
NC_000001.9:g.233996036G>C	NCBI36
NG_007397.1:g.122528C>G , LRG_143:g.122528C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461526.2:c.762C>G	ENSP00000513165.1:p.His254Gln
ENST00000697178.1:c.*1511C>G	ENSP00000513163.1:n.*1511C>G
ENST00000697180.1:c.592C>G
ENST00000697241.1:c.519C>G	ENSP00000513206.1:p.His173Gln
ENST00000389793.7:c.6087C>G MANE Select	ENSP00000374443.2:p.His2029Gln
ENST00000389793.6:c.6087C>G	ENSP00000374443.2:p.His2029Gln
ENST00000389794.7:c.*1511C>G	ENSP00000374444.4:n.*1511C>G
ENST00000489585.5:n.6512+126C>G
NM_000081.3:c.6087C>G , LRG_143t1:c.6087C>G	NP_000072.2:p.His2029Gln
NM_001301365.1:c.6087C>G , LRG_143t2:c.6087C>G	NP_001288294.1:p.His2029Gln
XM_011544031.1:c.6087C>G	XP_011542333.1:p.His2029Gln
XM_011544032.1:c.6087C>G	XP_011542334.1:p.His2029Gln
XM_011544033.1:c.6087C>G	XP_011542335.1:p.His2029Gln
XM_011544034.1:c.5949C>G	XP_011542336.1:p.His1983Gln
XM_011544035.1:c.6087C>G	XP_011542337.1:p.His2029Gln
XM_011544036.1:c.3750C>G	XP_011542338.1:p.His1250Gln
XM_011544037.1:c.6087C>G	XP_011542339.1:p.His2029Gln
XM_011544038.1:c.6087C>G	XP_011542340.1:p.His2029Gln
XM_011544039.1:c.6087C>G	XP_011542341.1:p.His2029Gln
XM_011544040.1:c.5996C>G	XP_011542342.1:p.Thr1999Arg
XM_011544033.2:c.6087C>G	XP_011542335.1:p.His2029Gln
XM_011544035.2:c.6087C>G	XP_011542337.1:p.His2029Gln
XM_011544036.2:c.3750C>G	XP_011542338.1:p.His1250Gln
XM_011544037.2:c.6087C>G	XP_011542339.1:p.His2029Gln
XM_011544039.2:c.6087C>G	XP_011542341.1:p.His2029Gln
XM_017000150.1:c.6087C>G	XP_016855639.1:p.His2029Gln
XM_017000151.1:c.5858C>G	XP_016855640.1:p.Thr1953Arg
XR_001736946.2:n.6269C>G
XR_001736947.1:n.6269C>G
XR_001736948.1:n.6269C>G
XR_002959252.1:n.6178C>G
NM_000081.4:c.6087C>G MANE Select	NP_000072.2:p.His2029Gln