Canonical Allele Identifier: CA344940980

Gene: LYST

Linked Data

• MyVariant Identifiers: chr1:g.235922597A>C (hg19) ; chr1:g.235759297A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235759297A>C , CM000663.2:g.235759297A>C	GRCh38
NC_000001.10:g.235922597A>C , CM000663.1:g.235922597A>C	GRCh37
NC_000001.9:g.233989220A>C	NCBI36
NG_007397.1:g.129344T>G , LRG_143:g.129344T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.1231T>G	ENSP00000513165.1:p.Ser411Ala
ENST00000697178.1:c.*1980T>G	ENSP00000513163.1:n.*1980T>G
ENST00000697236.1:c.265T>G	ENSP00000513203.1:p.Ser89Ala
ENST00000697241.1:c.988T>G	ENSP00000513206.1:p.Ser330Ala
ENST00000389793.7:c.6556T>G MANE Select	ENSP00000374443.2:p.Ser2186Ala
ENST00000389793.6:c.6556T>G	ENSP00000374443.2:p.Ser2186Ala
ENST00000389794.7:c.*1980T>G	ENSP00000374444.4:n.*1980T>G
ENST00000489585.5:n.6947T>G
NM_000081.3:c.6556T>G , LRG_143t1:c.6556T>G	NP_000072.2:p.Ser2186Ala
NM_001301365.1:c.6556T>G , LRG_143t2:c.6556T>G	NP_001288294.1:p.Ser2186Ala
XM_011544031.1:c.6556T>G	XP_011542333.1:p.Ser2186Ala
XM_011544032.1:c.6556T>G	XP_011542334.1:p.Ser2186Ala
XM_011544033.1:c.6556T>G	XP_011542335.1:p.Ser2186Ala
XM_011544034.1:c.6418T>G	XP_011542336.1:p.Ser2140Ala
XM_011544035.1:c.6556T>G	XP_011542337.1:p.Ser2186Ala
XM_011544036.1:c.4219T>G	XP_011542338.1:p.Ser1407Ala
XM_011544037.1:c.6556T>G	XP_011542339.1:p.Ser2186Ala
XM_011544038.1:c.6556T>G	XP_011542340.1:p.Ser2186Ala
XM_011544039.1:c.6556T>G	XP_011542341.1:p.Ser2186Ala
XM_011544033.2:c.6556T>G	XP_011542335.1:p.Ser2186Ala
XM_011544035.2:c.6556T>G	XP_011542337.1:p.Ser2186Ala
XM_011544036.2:c.4219T>G	XP_011542338.1:p.Ser1407Ala
XM_011544037.2:c.6556T>G	XP_011542339.1:p.Ser2186Ala
XM_011544039.2:c.6556T>G	XP_011542341.1:p.Ser2186Ala
XM_017000150.1:c.6556T>G	XP_016855639.1:p.Ser2186Ala
XR_001736946.2:n.6738T>G
XR_001736947.1:n.6738T>G
XR_001736948.1:n.6738T>G
NM_000081.4:c.6556T>G MANE Select	NP_000072.2:p.Ser2186Ala