Canonical Allele Identifier: CA344919985

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235733536C>T , CM000663.2:g.235733536C>T	GRCh38
NC_000001.10:g.235896836C>T , CM000663.1:g.235896836C>T	GRCh37
NC_000001.9:g.233963459C>T	NCBI36
NG_007397.1:g.155105G>A , LRG_143:g.155105G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.8768G>A MANE Select	NP_000072.2:p.Trp2923Ter
ENST00000389793.7:c.8768G>A MANE Select	ENSP00000374443.2:p.Trp2923Ter
NM_000081.3:c.8768G>A , LRG_143t1:c.8768G>A	NP_000072.2:p.Trp2923Ter
NM_001301365.1:c.8768G>A , LRG_143t2:c.8768G>A	NP_001288294.1:p.Trp2923Ter
ENST00000389793.6:c.8768G>A	ENSP00000374443.2:p.Trp2923Ter
ENST00000389794.7:c.*4192G>A	ENSP00000374444.4:n.*4192G>A
ENST00000461526.2:c.4296G>A	ENSP00000513165.1:n.4296G>A
ENST00000473037.5:n.3758G>A
ENST00000475277.2:c.863G>A	ENSP00000513164.1:p.Trp288Ter
ENST00000697178.1:c.*4192G>A	ENSP00000513163.1:n.*4192G>A
ENST00000697236.1:c.2477G>A	ENSP00000513203.1:p.Trp826Ter
ENST00000697240.1:c.902G>A	ENSP00000513205.1:p.Trp301Ter
ENST00000697241.1:c.3248G>A	ENSP00000513206.1:p.Trp1083Ter
XM_011544031.1:c.8930G>A	XP_011542333.1:p.Trp2977Ter
XM_011544032.1:c.8930G>A	XP_011542334.1:p.Trp2977Ter
XM_011544033.1:c.8930G>A	XP_011542335.1:p.Trp2977Ter
XM_011544033.2:c.8930G>A	XP_011542335.1:p.Trp2977Ter
XM_011544034.1:c.8792G>A	XP_011542336.1:p.Trp2931Ter
XM_011544035.1:c.8930G>A	XP_011542337.1:p.Trp2977Ter
XM_011544035.2:c.8930G>A	XP_011542337.1:p.Trp2977Ter
XM_011544036.1:c.6593G>A	XP_011542338.1:p.Trp2198Ter
XM_011544036.2:c.6593G>A	XP_011542338.1:p.Trp2198Ter
XM_017000150.1:c.8930G>A	XP_016855639.1:p.Trp2977Ter
XR_001736947.1:n.9803G>A