Canonical Allele Identifier: CA1465506

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235715209G>A , CM000663.2:g.235715209G>A	GRCh38
NC_000001.10:g.235878509G>A , CM000663.1:g.235878509G>A	GRCh37
NC_000001.9:g.233945132G>A	NCBI36
NG_007397.1:g.173432C>T , LRG_143:g.173432C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.5304C>T	ENSP00000513165.1:n.5304C>T
ENST00000475277.2:c.1871C>T	ENSP00000513164.1:p.Ala624Val
ENST00000697178.1:c.*5471C>T	ENSP00000513163.1:n.*5471C>T
ENST00000697235.1:c.326C>T	ENSP00000513202.1:p.Ala109Val
ENST00000697236.1:c.3240C>T	ENSP00000513203.1:n.3240C>T
ENST00000697237.1:c.732C>T
ENST00000697240.1:c.1910C>T	ENSP00000513205.1:p.Ala637Val
ENST00000389793.7:c.9776C>T MANE Select	ENSP00000374443.2:p.Ala3259Val
ENST00000389793.6:c.9776C>T	ENSP00000374443.2:p.Ala3259Val
ENST00000389794.7:c.*5200C>T	ENSP00000374444.4:n.*5200C>T
ENST00000473037.5:n.4766C>T
ENST00000475277.1:n.642C>T
NM_000081.3:c.9776C>T , LRG_143t1:c.9776C>T	NP_000072.2:p.Ala3259Val
NM_001301365.1:c.9776C>T , LRG_143t2:c.9776C>T	NP_001288294.1:p.Ala3259Val
XM_011544031.1:c.9938C>T	XP_011542333.1:p.Ala3313Val
XM_011544032.1:c.9938C>T	XP_011542334.1:p.Ala3313Val
XM_011544033.1:c.9938C>T	XP_011542335.1:p.Ala3313Val
XM_011544034.1:c.9800C>T	XP_011542336.1:p.Ala3267Val
XM_011544035.1:c.9938C>T	XP_011542337.1:p.Ala3313Val
XM_011544036.1:c.7601C>T	XP_011542338.1:p.Ala2534Val
XM_011544033.2:c.9938C>T	XP_011542335.1:p.Ala3313Val
XM_011544035.2:c.9938C>T	XP_011542337.1:p.Ala3313Val
XM_011544036.2:c.7601C>T	XP_011542338.1:p.Ala2534Val
XM_017000150.1:c.9938C>T	XP_016855639.1:p.Ala3313Val
XR_001736947.1:n.10811C>T
NM_000081.4:c.9776C>T MANE Select	NP_000072.2:p.Ala3259Val