Canonical Allele Identifier: CA344945802

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235724143C>T , CM000663.2:g.235724143C>T	GRCh38
NC_000001.10:g.235887443C>T , CM000663.1:g.235887443C>T	GRCh37
NC_000001.9:g.233954066C>T	NCBI36
NG_007397.1:g.164498G>A , LRG_143:g.164498G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.9200G>A MANE Select	NP_000072.2:p.Trp3067Ter
ENST00000389793.7:c.9200G>A MANE Select	ENSP00000374443.2:p.Trp3067Ter
NM_000081.3:c.9200G>A , LRG_143t1:c.9200G>A	NP_000072.2:p.Trp3067Ter
NM_001301365.1:c.9200G>A , LRG_143t2:c.9200G>A	NP_001288294.1:p.Trp3067Ter
ENST00000389793.6:c.9200G>A	ENSP00000374443.2:p.Trp3067Ter
ENST00000389794.7:c.*4624G>A	ENSP00000374444.4:n.*4624G>A
ENST00000461526.2:c.4728G>A	ENSP00000513165.1:n.4728G>A
ENST00000473037.5:n.4190G>A
ENST00000475277.1:n.66G>A
ENST00000475277.2:c.1295G>A	ENSP00000513164.1:p.Trp432Ter
ENST00000697178.1:c.*4624G>A	ENSP00000513163.1:n.*4624G>A
ENST00000697236.1:c.2909G>A	ENSP00000513203.1:p.Trp970Ter
ENST00000697237.1:c.156G>A
ENST00000697240.1:c.1334G>A	ENSP00000513205.1:p.Trp445Ter
ENST00000697241.1:c.3680G>A	ENSP00000513206.1:p.Trp1227Ter
XM_011544031.1:c.9362G>A	XP_011542333.1:p.Trp3121Ter
XM_011544032.1:c.9362G>A	XP_011542334.1:p.Trp3121Ter
XM_011544033.1:c.9362G>A	XP_011542335.1:p.Trp3121Ter
XM_011544033.2:c.9362G>A	XP_011542335.1:p.Trp3121Ter
XM_011544034.1:c.9224G>A	XP_011542336.1:p.Trp3075Ter
XM_011544035.1:c.9362G>A	XP_011542337.1:p.Trp3121Ter
XM_011544035.2:c.9362G>A	XP_011542337.1:p.Trp3121Ter
XM_011544036.1:c.7025G>A	XP_011542338.1:p.Trp2342Ter
XM_011544036.2:c.7025G>A	XP_011542338.1:p.Trp2342Ter
XM_017000150.1:c.9362G>A	XP_016855639.1:p.Trp3121Ter
XR_001736947.1:n.10235G>A