Canonical Allele Identifier: CA1465201

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235664492G>A , CM000663.2:g.235664492G>A	GRCh38
NC_000001.10:g.235827792G>A , CM000663.1:g.235827792G>A	GRCh37
NC_000001.9:g.233894415G>A	NCBI36
NG_007397.1:g.224149C>T , LRG_143:g.224149C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462376.2:n.2578C>T
ENST00000697178.1:c.*7154C>T	ENSP00000513163.1:n.*7154C>T
ENST00000697235.1:c.1718C>T	ENSP00000513202.1:p.Ala573Val
ENST00000697236.1:c.4632C>T	ENSP00000513203.1:n.4632C>T
ENST00000697237.1:c.1879C>T
ENST00000697238.1:n.322C>T
ENST00000697239.1:n.562C>T
ENST00000697240.1:c.3235C>T	ENSP00000513205.1:n.3235C>T
ENST00000389793.7:c.11168C>T MANE Select	ENSP00000374443.2:p.Ala3723Val
ENST00000389793.6:c.11168C>T	ENSP00000374443.2:p.Ala3723Val
ENST00000389794.7:c.*6592C>T	ENSP00000374444.4:n.*6592C>T
ENST00000473037.5:n.6158C>T
NM_000081.3:c.11168C>T , LRG_143t1:c.11168C>T	NP_000072.2:p.Ala3723Val
NM_001301365.1:c.11168C>T , LRG_143t2:c.11168C>T	NP_001288294.1:p.Ala3723Val
XM_011544031.1:c.11330C>T	XP_011542333.1:p.Ala3777Val
XM_011544032.1:c.11330C>T	XP_011542334.1:p.Ala3777Val
XM_011544033.1:c.11330C>T	XP_011542335.1:p.Ala3777Val
XM_011544034.1:c.11192C>T	XP_011542336.1:p.Ala3731Val
XM_011544036.1:c.8993C>T	XP_011542338.1:p.Ala2998Val
XM_011544033.2:c.11330C>T	XP_011542335.1:p.Ala3777Val
XM_011544036.2:c.8993C>T	XP_011542338.1:p.Ala2998Val
XM_017000150.1:c.11099C>T	XP_016855639.1:p.Ala3700Val
NM_000081.4:c.11168C>T MANE Select	NP_000072.2:p.Ala3723Val