Canonical Allele Identifier: CA1141188093

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235733859C= , CM000663.2:g.235733859C=	GRCh38
NC_000001.10:g.235897159C= , CM000663.1:g.235897159C=	GRCh37
NC_000001.9:g.233963782C=	NCBI36
NG_007397.1:g.154782G= , LRG_143:g.154782G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.4111G=	ENSP00000513165.1:n.4111G=
ENST00000475277.2:c.678G=	ENSP00000513164.1:p.Trp226=
ENST00000697178.1:c.*4007G=	ENSP00000513163.1:n.*4007G=
ENST00000697236.1:c.2292G=	ENSP00000513203.1:p.Trp764=
ENST00000697240.1:c.717G=	ENSP00000513205.1:p.Trp239=
ENST00000697241.1:c.3063G=	ENSP00000513206.1:p.Trp1021=
ENST00000389793.7:c.8583G= MANE Select	ENSP00000374443.2:p.Trp2861=
ENST00000389793.6:c.8583G=	ENSP00000374443.2:p.Trp2861=
ENST00000389794.7:c.*4007G=	ENSP00000374444.4:n.*4007G=
ENST00000473037.5:n.3573G=
NM_000081.3:c.8583G= , LRG_143t1:c.8583G=	NP_000072.2:p.Trp2861=
NM_001301365.1:c.8583G= , LRG_143t2:c.8583G=	NP_001288294.1:p.Trp2861=
XM_011544031.1:c.8745G=	XP_011542333.1:p.Trp2915=
XM_011544032.1:c.8745G=	XP_011542334.1:p.Trp2915=
XM_011544033.1:c.8745G=	XP_011542335.1:p.Trp2915=
XM_011544034.1:c.8607G=	XP_011542336.1:p.Trp2869=
XM_011544035.1:c.8745G=	XP_011542337.1:p.Trp2915=
XM_011544036.1:c.6408G=	XP_011542338.1:p.Trp2136=
XM_011544033.2:c.8745G=	XP_011542335.1:p.Trp2915=
XM_011544035.2:c.8745G=	XP_011542337.1:p.Trp2915=
XM_011544036.2:c.6408G=	XP_011542338.1:p.Trp2136=
XM_017000150.1:c.8745G=	XP_016855639.1:p.Trp2915=
XR_001736947.1:n.9618G=
NM_000081.4:c.8583G= MANE Select	NP_000072.2:p.Trp2861=