Canonical Allele Identifier: CA344942405

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235759473C>T , CM000663.2:g.235759473C>T	GRCh38
NC_000001.10:g.235922773C>T , CM000663.1:g.235922773C>T	GRCh37
NC_000001.9:g.233989396C>T	NCBI36
NG_007397.1:g.129168G>A , LRG_143:g.129168G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.1055G>A	ENSP00000513165.1:p.Cys352Tyr
ENST00000697178.1:c.*1804G>A	ENSP00000513163.1:n.*1804G>A
ENST00000697180.1:c.885G>A
ENST00000697236.1:c.89G>A	ENSP00000513203.1:p.Cys30Tyr
ENST00000697241.1:c.812G>A	ENSP00000513206.1:p.Cys271Tyr
ENST00000389793.7:c.6380G>A MANE Select	ENSP00000374443.2:p.Cys2127Tyr
ENST00000389793.6:c.6380G>A	ENSP00000374443.2:p.Cys2127Tyr
ENST00000389794.7:c.*1804G>A	ENSP00000374444.4:n.*1804G>A
ENST00000489585.5:n.6771G>A
NM_000081.3:c.6380G>A , LRG_143t1:c.6380G>A	NP_000072.2:p.Cys2127Tyr
NM_001301365.1:c.6380G>A , LRG_143t2:c.6380G>A	NP_001288294.1:p.Cys2127Tyr
XM_011544031.1:c.6380G>A	XP_011542333.1:p.Cys2127Tyr
XM_011544032.1:c.6380G>A	XP_011542334.1:p.Cys2127Tyr
XM_011544033.1:c.6380G>A	XP_011542335.1:p.Cys2127Tyr
XM_011544034.1:c.6242G>A	XP_011542336.1:p.Cys2081Tyr
XM_011544035.1:c.6380G>A	XP_011542337.1:p.Cys2127Tyr
XM_011544036.1:c.4043G>A	XP_011542338.1:p.Cys1348Tyr
XM_011544037.1:c.6380G>A	XP_011542339.1:p.Cys2127Tyr
XM_011544038.1:c.6380G>A	XP_011542340.1:p.Cys2127Tyr
XM_011544039.1:c.6380G>A	XP_011542341.1:p.Cys2127Tyr
XM_011544033.2:c.6380G>A	XP_011542335.1:p.Cys2127Tyr
XM_011544035.2:c.6380G>A	XP_011542337.1:p.Cys2127Tyr
XM_011544036.2:c.4043G>A	XP_011542338.1:p.Cys1348Tyr
XM_011544037.2:c.6380G>A	XP_011542339.1:p.Cys2127Tyr
XM_011544039.2:c.6380G>A	XP_011542341.1:p.Cys2127Tyr
XM_017000150.1:c.6380G>A	XP_016855639.1:p.Cys2127Tyr
XR_001736946.2:n.6562G>A
XR_001736947.1:n.6562G>A
XR_001736948.1:n.6562G>A
XR_002959252.1:n.6471G>A
NM_000081.4:c.6380G>A MANE Select	NP_000072.2:p.Cys2127Tyr