Canonical Allele Identifier: CA344920780

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235733907C>T , CM000663.2:g.235733907C>T	GRCh38
NC_000001.10:g.235897207C>T , CM000663.1:g.235897207C>T	GRCh37
NC_000001.9:g.233963830C>T	NCBI36
NG_007397.1:g.154734G>A , LRG_143:g.154734G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.8536-1G>A MANE Select	NP_000072.2:n.8536-1G>A
ENST00000389793.7:c.8536-1G>A MANE Select	ENSP00000374443.2:n.8536-1G>A
NM_000081.3:c.8536-1G>A , LRG_143t1:c.8536-1G>A	NP_000072.2:n.8536-1G>A
NM_001301365.1:c.8536-1G>A , LRG_143t2:c.8536-1G>A	NP_001288294.1:n.8536-1G>A
ENST00000389793.6:c.8536-1G>A	ENSP00000374443.2:n.8536-1G>A
ENST00000389794.7:c.*3960-1G>A	ENSP00000374444.4:n.*3960-1G>A
ENST00000461526.2:c.4064-1G>A	ENSP00000513165.1:n.4064-1G>A
ENST00000473037.5:n.3526-1G>A
ENST00000475277.2:c.631-1G>A	ENSP00000513164.1:n.631-1G>A
ENST00000697178.1:c.*3960-1G>A	ENSP00000513163.1:n.*3960-1G>A
ENST00000697236.1:c.2245-1G>A	ENSP00000513203.1:n.2245-1G>A
ENST00000697240.1:c.670-1G>A	ENSP00000513205.1:n.670-1G>A
ENST00000697241.1:c.3016-1G>A	ENSP00000513206.1:n.3016-1G>A
XM_011544031.1:c.8698-1G>A	XP_011542333.1:n.8698-1G>A
XM_011544032.1:c.8698-1G>A	XP_011542334.1:n.8698-1G>A
XM_011544033.1:c.8698-1G>A	XP_011542335.1:n.8698-1G>A
XM_011544033.2:c.8698-1G>A	XP_011542335.1:n.8698-1G>A
XM_011544034.1:c.8560-1G>A	XP_011542336.1:n.8560-1G>A
XM_011544035.1:c.8698-1G>A	XP_011542337.1:n.8698-1G>A
XM_011544035.2:c.8698-1G>A	XP_011542337.1:n.8698-1G>A
XM_011544036.1:c.6361-1G>A	XP_011542338.1:n.6361-1G>A
XM_011544036.2:c.6361-1G>A	XP_011542338.1:n.6361-1G>A
XM_017000150.1:c.8698-1G>A	XP_016855639.1:n.8698-1G>A
XR_001736947.1:n.9571-1G>A