Canonical Allele Identifier: CA1466003

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235746437C>T , CM000663.2:g.235746437C>T	GRCh38
NC_000001.10:g.235909737C>T , CM000663.1:g.235909737C>T	GRCh37
NC_000001.9:g.233976360C>T	NCBI36
NG_007397.1:g.142204G>A , LRG_143:g.142204G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.2546G>A	ENSP00000513165.1:p.Arg849Gln
ENST00000697178.1:c.*3295G>A	ENSP00000513163.1:n.*3295G>A
ENST00000697236.1:c.1580G>A	ENSP00000513203.1:p.Arg527Gln
ENST00000697240.1:c.5G>A	ENSP00000513205.1:p.Arg2Gln
ENST00000697241.1:c.2351G>A	ENSP00000513206.1:p.Arg784Gln
ENST00000389793.7:c.7871G>A MANE Select	ENSP00000374443.2:p.Arg2624Gln
ENST00000389793.6:c.7871G>A	ENSP00000374443.2:p.Arg2624Gln
ENST00000389794.7:c.*3295G>A	ENSP00000374444.4:n.*3295G>A
NM_000081.3:c.7871G>A , LRG_143t1:c.7871G>A	NP_000072.2:p.Arg2624Gln
NM_001301365.1:c.7871G>A , LRG_143t2:c.7871G>A	NP_001288294.1:p.Arg2624Gln
XM_011544031.1:c.8033G>A	XP_011542333.1:p.Arg2678Gln
XM_011544032.1:c.8033G>A	XP_011542334.1:p.Arg2678Gln
XM_011544033.1:c.8033G>A	XP_011542335.1:p.Arg2678Gln
XM_011544034.1:c.7895G>A	XP_011542336.1:p.Arg2632Gln
XM_011544035.1:c.8033G>A	XP_011542337.1:p.Arg2678Gln
XM_011544036.1:c.5696G>A	XP_011542338.1:p.Arg1899Gln
XM_011544037.1:c.8033G>A	XP_011542339.1:p.Arg2678Gln
XM_011544038.1:c.8033G>A	XP_011542340.1:p.Arg2678Gln
XM_011544033.2:c.8033G>A	XP_011542335.1:p.Arg2678Gln
XM_011544035.2:c.8033G>A	XP_011542337.1:p.Arg2678Gln
XM_011544036.2:c.5696G>A	XP_011542338.1:p.Arg1899Gln
XM_011544037.2:c.8033G>A	XP_011542339.1:p.Arg2678Gln
XM_017000150.1:c.8033G>A	XP_016855639.1:p.Arg2678Gln
XR_001736946.2:n.8215G>A
XR_001736947.1:n.8053G>A
XR_001736948.1:n.7502G>A
NM_000081.4:c.7871G>A MANE Select	NP_000072.2:p.Arg2624Gln