Canonical Allele Identifier: CA2486625452

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235741499T= , CM000663.2:g.235741499T=	GRCh38
NC_000001.10:g.235904799T= , CM000663.1:g.235904799T=	GRCh37
NC_000001.9:g.233971422T=	NCBI36
NG_007397.1:g.147142A= , LRG_143:g.147142A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.8281A= MANE Select	NP_000072.2:p.Arg2761=
ENST00000389793.7:c.8281A= MANE Select	ENSP00000374443.2:p.Arg2761=
NM_000081.3:c.8281A= , LRG_143t1:c.8281A=	NP_000072.2:p.Arg2761=
NM_001301365.1:c.8281A= , LRG_143t2:c.8281A=	NP_001288294.1:p.Arg2761=
ENST00000389793.6:c.8281A=	ENSP00000374443.2:p.Arg2761=
ENST00000389794.7:c.*3705A=	ENSP00000374444.4:n.*3705A=
ENST00000461526.1:n.184A=
ENST00000461526.2:c.2956A=	ENSP00000513165.1:p.Arg986=
ENST00000475277.2:c.376A=	ENSP00000513164.1:p.Arg126=
ENST00000697178.1:c.*3705A=	ENSP00000513163.1:n.*3705A=
ENST00000697236.1:c.1990A=	ENSP00000513203.1:p.Arg664=
ENST00000697240.1:c.415A=	ENSP00000513205.1:p.Arg139=
ENST00000697241.1:c.2761A=	ENSP00000513206.1:p.Arg921=
XM_011544031.1:c.8443A=	XP_011542333.1:p.Arg2815=
XM_011544032.1:c.8443A=	XP_011542334.1:p.Arg2815=
XM_011544033.1:c.8443A=	XP_011542335.1:p.Arg2815=
XM_011544033.2:c.8443A=	XP_011542335.1:p.Arg2815=
XM_011544034.1:c.8305A=	XP_011542336.1:p.Arg2769=
XM_011544035.1:c.8443A=	XP_011542337.1:p.Arg2815=
XM_011544035.2:c.8443A=	XP_011542337.1:p.Arg2815=
XM_011544036.1:c.6106A=	XP_011542338.1:p.Arg2036=
XM_011544036.2:c.6106A=	XP_011542338.1:p.Arg2036=
XM_011544037.1:c.8443A=	XP_011542339.1:p.Arg2815=
XM_011544037.2:c.8443A=	XP_011542339.1:p.Arg2815=
XM_011544038.1:c.8443A=	XP_011542340.1:p.Arg2815=
XM_017000150.1:c.8443A=	XP_016855639.1:p.Arg2815=
XR_001736946.2:n.8625A=
XR_001736947.1:n.8463A=
XR_001736948.1:n.7912A=