Canonical Allele Identifier: CA1141188109

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235709107T= , CM000663.2:g.235709107T=	GRCh38
NC_000001.10:g.235872407T= , CM000663.1:g.235872407T=	GRCh37
NC_000001.9:g.233939030T=	NCBI36
NG_007397.1:g.179534A= , LRG_143:g.179534A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462376.2:n.1537A=
ENST00000697178.1:c.*5822A=	ENSP00000513163.1:n.*5822A=
ENST00000697179.1:n.2836A=
ENST00000697235.1:c.677A=	ENSP00000513202.1:p.Asn226=
ENST00000697236.1:c.3591A=	ENSP00000513203.1:n.3591A=
ENST00000697237.1:c.838A=
ENST00000697240.1:c.2261A=	ENSP00000513205.1:p.Asn754=
ENST00000389793.7:c.10127A= MANE Select	ENSP00000374443.2:p.Asn3376=
ENST00000389793.6:c.10127A=	ENSP00000374443.2:p.Asn3376=
ENST00000389794.7:c.*5551A=	ENSP00000374444.4:n.*5551A=
ENST00000462376.1:n.546A=
ENST00000473037.5:n.5117A=
NM_000081.3:c.10127A= , LRG_143t1:c.10127A=	NP_000072.2:p.Asn3376=
NM_001301365.1:c.10127A= , LRG_143t2:c.10127A=	NP_001288294.1:p.Asn3376=
XM_011544031.1:c.10289A=	XP_011542333.1:p.Asn3430=
XM_011544032.1:c.10289A=	XP_011542334.1:p.Asn3430=
XM_011544033.1:c.10289A=	XP_011542335.1:p.Asn3430=
XM_011544034.1:c.10151A=	XP_011542336.1:p.Asn3384=
XM_011544036.1:c.7952A=	XP_011542338.1:p.Asn2651=
XM_011544033.2:c.10289A=	XP_011542335.1:p.Asn3430=
XM_011544036.2:c.7952A=	XP_011542338.1:p.Asn2651=
XM_017000150.1:c.10289A=	XP_016855639.1:p.Asn3430=
NM_000081.4:c.10127A= MANE Select	NP_000072.2:p.Asn3376=