Canonical Allele Identifier: CA1466004

Gene: LYST

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235746438G>A , CM000663.2:g.235746438G>A	GRCh38
NC_000001.10:g.235909738G>A , CM000663.1:g.235909738G>A	GRCh37
NC_000001.9:g.233976361G>A	NCBI36
NG_007397.1:g.142203C>T , LRG_143:g.142203C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.2545C>T	ENSP00000513165.1:p.Arg849Trp
ENST00000697178.1:c.*3294C>T	ENSP00000513163.1:n.*3294C>T
ENST00000697236.1:c.1579C>T	ENSP00000513203.1:p.Arg527Trp
ENST00000697240.1:c.4C>T	ENSP00000513205.1:p.Arg2Trp
ENST00000697241.1:c.2350C>T	ENSP00000513206.1:p.Arg784Trp
ENST00000389793.7:c.7870C>T MANE Select	ENSP00000374443.2:p.Arg2624Trp
ENST00000389793.6:c.7870C>T	ENSP00000374443.2:p.Arg2624Trp
ENST00000389794.7:c.*3294C>T	ENSP00000374444.4:n.*3294C>T
NM_000081.3:c.7870C>T , LRG_143t1:c.7870C>T	NP_000072.2:p.Arg2624Trp
NM_001301365.1:c.7870C>T , LRG_143t2:c.7870C>T	NP_001288294.1:p.Arg2624Trp
XM_011544031.1:c.8032C>T	XP_011542333.1:p.Arg2678Trp
XM_011544032.1:c.8032C>T	XP_011542334.1:p.Arg2678Trp
XM_011544033.1:c.8032C>T	XP_011542335.1:p.Arg2678Trp
XM_011544034.1:c.7894C>T	XP_011542336.1:p.Arg2632Trp
XM_011544035.1:c.8032C>T	XP_011542337.1:p.Arg2678Trp
XM_011544036.1:c.5695C>T	XP_011542338.1:p.Arg1899Trp
XM_011544037.1:c.8032C>T	XP_011542339.1:p.Arg2678Trp
XM_011544038.1:c.8032C>T	XP_011542340.1:p.Arg2678Trp
XM_011544033.2:c.8032C>T	XP_011542335.1:p.Arg2678Trp
XM_011544035.2:c.8032C>T	XP_011542337.1:p.Arg2678Trp
XM_011544036.2:c.5695C>T	XP_011542338.1:p.Arg1899Trp
XM_011544037.2:c.8032C>T	XP_011542339.1:p.Arg2678Trp
XM_017000150.1:c.8032C>T	XP_016855639.1:p.Arg2678Trp
XR_001736946.2:n.8214C>T
XR_001736947.1:n.8052C>T
XR_001736948.1:n.7501C>T
NM_000081.4:c.7870C>T MANE Select	NP_000072.2:p.Arg2624Trp