Canonical Allele Identifier: CA1141188094

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235734590C= , CM000663.2:g.235734590C=	GRCh38
NC_000001.10:g.235897890C= , CM000663.1:g.235897890C=	GRCh37
NC_000001.9:g.233964513C=	NCBI36
NG_007397.1:g.154051G= , LRG_143:g.154051G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.3956G=	ENSP00000513165.1:n.3956G=
ENST00000475277.2:c.523G=	ENSP00000513164.1:p.Glu175=
ENST00000697178.1:c.*3852G=	ENSP00000513163.1:n.*3852G=
ENST00000697236.1:c.2137G=	ENSP00000513203.1:p.Glu713=
ENST00000697240.1:c.562G=	ENSP00000513205.1:p.Glu188=
ENST00000697241.1:c.2908G=	ENSP00000513206.1:p.Glu970=
ENST00000389793.7:c.8428G= MANE Select	ENSP00000374443.2:p.Glu2810=
ENST00000389793.6:c.8428G=	ENSP00000374443.2:p.Glu2810=
ENST00000389794.7:c.*3852G=	ENSP00000374444.4:n.*3852G=
ENST00000473037.5:n.3418G=
NM_000081.3:c.8428G= , LRG_143t1:c.8428G=	NP_000072.2:p.Glu2810=
NM_001301365.1:c.8428G= , LRG_143t2:c.8428G=	NP_001288294.1:p.Glu2810=
XM_011544031.1:c.8590G=	XP_011542333.1:p.Glu2864=
XM_011544032.1:c.8590G=	XP_011542334.1:p.Glu2864=
XM_011544033.1:c.8590G=	XP_011542335.1:p.Glu2864=
XM_011544034.1:c.8452G=	XP_011542336.1:p.Glu2818=
XM_011544035.1:c.8590G=	XP_011542337.1:p.Glu2864=
XM_011544036.1:c.6253G=	XP_011542338.1:p.Glu2085=
XM_011544033.2:c.8590G=	XP_011542335.1:p.Glu2864=
XM_011544035.2:c.8590G=	XP_011542337.1:p.Glu2864=
XM_011544036.2:c.6253G=	XP_011542338.1:p.Glu2085=
XM_017000150.1:c.8590G=	XP_016855639.1:p.Glu2864=
XR_001736947.1:n.9463G=
NM_000081.4:c.8428G= MANE Select	NP_000072.2:p.Glu2810=