Canonical Allele Identifier: CA1467578

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235810126T>C , CM000663.2:g.235810126T>C	GRCh38
NC_000001.10:g.235973426T>C , CM000663.1:g.235973426T>C	GRCh37
NC_000001.9:g.234040049T>C	NCBI36
NG_007397.1:g.78515A>G , LRG_143:g.78515A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.692A>G MANE Select	NP_000072.2:p.Gln231Arg
ENST00000389793.7:c.692A>G MANE Select	ENSP00000374443.2:p.Gln231Arg
NM_000081.3:c.692A>G , LRG_143t1:c.692A>G	NP_000072.2:p.Gln231Arg
NM_001301365.1:c.692A>G , LRG_143t2:c.692A>G	NP_001288294.1:p.Gln231Arg
ENST00000389793.6:c.692A>G	ENSP00000374443.2:p.Gln231Arg
ENST00000389794.7:c.692A>G	ENSP00000374444.4:p.Gln231Arg
ENST00000465349.5:n.1243A>G
ENST00000489585.5:n.1243A>G
ENST00000697178.1:c.692A>G	ENSP00000513163.1:p.Gln231Arg
ENST00000697242.1:c.284-189A>G	ENSP00000513207.1:n.284-189A>G
XM_011544031.1:c.692A>G	XP_011542333.1:p.Gln231Arg
XM_011544032.1:c.692A>G	XP_011542334.1:p.Gln231Arg
XM_011544033.1:c.692A>G	XP_011542335.1:p.Gln231Arg
XM_011544033.2:c.692A>G	XP_011542335.1:p.Gln231Arg
XM_011544034.1:c.692A>G	XP_011542336.1:p.Gln231Arg
XM_011544035.1:c.692A>G	XP_011542337.1:p.Gln231Arg
XM_011544035.2:c.692A>G	XP_011542337.1:p.Gln231Arg
XM_011544037.1:c.692A>G	XP_011542339.1:p.Gln231Arg
XM_011544037.2:c.692A>G	XP_011542339.1:p.Gln231Arg
XM_011544038.1:c.692A>G	XP_011542340.1:p.Gln231Arg
XM_011544039.1:c.692A>G	XP_011542341.1:p.Gln231Arg
XM_011544039.2:c.692A>G	XP_011542341.1:p.Gln231Arg
XM_011544040.1:c.692A>G	XP_011542342.1:p.Gln231Arg
XM_017000150.1:c.692A>G	XP_016855639.1:p.Gln231Arg
XM_017000151.1:c.692A>G	XP_016855640.1:p.Gln231Arg
XR_001736946.2:n.874A>G
XR_001736947.1:n.874A>G
XR_001736948.1:n.874A>G
XR_002959252.1:n.874A>G