Canonical Allele Identifier: CA2486632338

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235759282G= , CM000663.2:g.235759282G=	GRCh38
NC_000001.10:g.235922582G= , CM000663.1:g.235922582G=	GRCh37
NC_000001.9:g.233989205G=	NCBI36
NG_007397.1:g.129359C= , LRG_143:g.129359C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.1246C=	ENSP00000513165.1:p.Pro416=
ENST00000697178.1:c.*1995C=	ENSP00000513163.1:n.*1995C=
ENST00000697236.1:c.280C=	ENSP00000513203.1:p.Pro94=
ENST00000697241.1:c.1003C=	ENSP00000513206.1:p.Pro335=
ENST00000389793.7:c.6571C= MANE Select	ENSP00000374443.2:p.Pro2191=
ENST00000389793.6:c.6571C=	ENSP00000374443.2:p.Pro2191=
ENST00000389794.7:c.*1995C=	ENSP00000374444.4:n.*1995C=
ENST00000489585.5:n.6962C=
NM_000081.3:c.6571C= , LRG_143t1:c.6571C=	NP_000072.2:p.Pro2191=
NM_001301365.1:c.6571C= , LRG_143t2:c.6571C=	NP_001288294.1:p.Pro2191=
XM_011544031.1:c.6571C=	XP_011542333.1:p.Pro2191=
XM_011544032.1:c.6571C=	XP_011542334.1:p.Pro2191=
XM_011544033.1:c.6571C=	XP_011542335.1:p.Pro2191=
XM_011544034.1:c.6433C=	XP_011542336.1:p.Pro2145=
XM_011544035.1:c.6571C=	XP_011542337.1:p.Pro2191=
XM_011544036.1:c.4234C=	XP_011542338.1:p.Pro1412=
XM_011544037.1:c.6571C=	XP_011542339.1:p.Pro2191=
XM_011544038.1:c.6571C=	XP_011542340.1:p.Pro2191=
XM_011544039.1:c.6571C=	XP_011542341.1:p.Pro2191=
XM_011544033.2:c.6571C=	XP_011542335.1:p.Pro2191=
XM_011544035.2:c.6571C=	XP_011542337.1:p.Pro2191=
XM_011544036.2:c.4234C=	XP_011542338.1:p.Pro1412=
XM_011544037.2:c.6571C=	XP_011542339.1:p.Pro2191=
XM_011544039.2:c.6571C=	XP_011542341.1:p.Pro2191=
XM_017000150.1:c.6571C=	XP_016855639.1:p.Pro2191=
XR_001736946.2:n.6753C=
XR_001736947.1:n.6753C=
XR_001736948.1:n.6753C=
NM_000081.4:c.6571C= MANE Select	NP_000072.2:p.Pro2191=