Canonical Allele Identifier: CA1141188111

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235716749T= , CM000663.2:g.235716749T=	GRCh38
NC_000001.10:g.235880049T= , CM000663.1:g.235880049T=	GRCh37
NC_000001.9:g.233946672T=	NCBI36
NG_007397.1:g.171892A= , LRG_143:g.171892A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.5118A=	ENSP00000513165.1:n.5118A=
ENST00000475277.2:c.1685A=	ENSP00000513164.1:p.Tyr562=
ENST00000697178.1:c.*5285A=	ENSP00000513163.1:n.*5285A=
ENST00000697235.1:c.140A=	ENSP00000513202.1:p.Tyr47=
ENST00000697236.1:c.3054A=	ENSP00000513203.1:n.3054A=
ENST00000697237.1:c.546A=
ENST00000697240.1:c.1724A=	ENSP00000513205.1:p.Tyr575=
ENST00000697241.1:c.4070A=	ENSP00000513206.1:p.Tyr1357=
ENST00000389793.7:c.9590A= MANE Select	ENSP00000374443.2:p.Tyr3197=
ENST00000389793.6:c.9590A=	ENSP00000374443.2:p.Tyr3197=
ENST00000389794.7:c.*5014A=	ENSP00000374444.4:n.*5014A=
ENST00000473037.5:n.4580A=
ENST00000475277.1:n.456A=
NM_000081.3:c.9590A= , LRG_143t1:c.9590A=	NP_000072.2:p.Tyr3197=
NM_001301365.1:c.9590A= , LRG_143t2:c.9590A=	NP_001288294.1:p.Tyr3197=
XM_011544031.1:c.9752A=	XP_011542333.1:p.Tyr3251=
XM_011544032.1:c.9752A=	XP_011542334.1:p.Tyr3251=
XM_011544033.1:c.9752A=	XP_011542335.1:p.Tyr3251=
XM_011544034.1:c.9614A=	XP_011542336.1:p.Tyr3205=
XM_011544035.1:c.9752A=	XP_011542337.1:p.Tyr3251=
XM_011544036.1:c.7415A=	XP_011542338.1:p.Tyr2472=
XM_011544033.2:c.9752A=	XP_011542335.1:p.Tyr3251=
XM_011544035.2:c.9752A=	XP_011542337.1:p.Tyr3251=
XM_011544036.2:c.7415A=	XP_011542338.1:p.Tyr2472=
XM_017000150.1:c.9752A=	XP_016855639.1:p.Tyr3251=
XR_001736947.1:n.10625A=
NM_000081.4:c.9590A= MANE Select	NP_000072.2:p.Tyr3197=