Canonical Allele Identifier: CA1466885

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235791976G>T , CM000663.2:g.235791976G>T	GRCh38
NC_000001.10:g.235955276G>T , CM000663.1:g.235955276G>T	GRCh37
NC_000001.9:g.234021899G>T	NCBI36
NG_007397.1:g.96665C>A , LRG_143:g.96665C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.4266C>A MANE Select	NP_000072.2:p.Ala1422=
ENST00000389793.7:c.4266C>A MANE Select	ENSP00000374443.2:p.Ala1422=
NM_000081.3:c.4266C>A , LRG_143t1:c.4266C>A	NP_000072.2:p.Ala1422=
NM_001301365.1:c.4266C>A , LRG_143t2:c.4266C>A	NP_001288294.1:p.Ala1422=
ENST00000389793.6:c.4266C>A	ENSP00000374443.2:p.Ala1422=
ENST00000389794.7:c.4116+1527C>A	ENSP00000374444.4:n.4116+1527C>A
ENST00000465349.5:n.4817C>A
ENST00000489585.5:n.4817C>A
ENST00000697178.1:c.4116+1527C>A	ENSP00000513163.1:n.4116+1527C>A
ENST00000697242.1:c.3669C>A	ENSP00000513207.1:p.Ala1223=
XM_011544031.1:c.4266C>A	XP_011542333.1:p.Ala1422=
XM_011544032.1:c.4266C>A	XP_011542334.1:p.Ala1422=
XM_011544033.1:c.4266C>A	XP_011542335.1:p.Ala1422=
XM_011544033.2:c.4266C>A	XP_011542335.1:p.Ala1422=
XM_011544034.1:c.4266C>A	XP_011542336.1:p.Ala1422=
XM_011544035.1:c.4266C>A	XP_011542337.1:p.Ala1422=
XM_011544035.2:c.4266C>A	XP_011542337.1:p.Ala1422=
XM_011544036.1:c.1929C>A	XP_011542338.1:p.Ala643=
XM_011544036.2:c.1929C>A	XP_011542338.1:p.Ala643=
XM_011544037.1:c.4266C>A	XP_011542339.1:p.Ala1422=
XM_011544037.2:c.4266C>A	XP_011542339.1:p.Ala1422=
XM_011544038.1:c.4266C>A	XP_011542340.1:p.Ala1422=
XM_011544039.1:c.4266C>A	XP_011542341.1:p.Ala1422=
XM_011544039.2:c.4266C>A	XP_011542341.1:p.Ala1422=
XM_011544040.1:c.4266C>A	XP_011542342.1:p.Ala1422=
XM_017000150.1:c.4266C>A	XP_016855639.1:p.Ala1422=
XM_017000151.1:c.4266C>A	XP_016855640.1:p.Ala1422=
XR_001736946.2:n.4448C>A
XR_001736947.1:n.4448C>A
XR_001736948.1:n.4448C>A
XR_002959252.1:n.4448C>A