Canonical Allele Identifier: CA423775952

Gene: LYST

Linked Data

• MyVariant Identifiers: chr1:g.235929419A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235766119A>G , CM000663.2:g.235766119A>G	GRCh38
NC_000001.10:g.235929419A>G , CM000663.1:g.235929419A>G	GRCh37
NC_000001.9:g.233996042A>G	NCBI36
NG_007397.1:g.122522T>C , LRG_143:g.122522T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.756T>C	ENSP00000513165.1:p.Val252=
ENST00000697178.1:c.*1505T>C	ENSP00000513163.1:n.*1505T>C
ENST00000697180.1:c.586T>C
ENST00000697241.1:c.513T>C	ENSP00000513206.1:p.Val171=
ENST00000389793.7:c.6081T>C MANE Select	ENSP00000374443.2:p.Val2027=
ENST00000389793.6:c.6081T>C	ENSP00000374443.2:p.Val2027=
ENST00000389794.7:c.*1505T>C	ENSP00000374444.4:n.*1505T>C
ENST00000489585.5:n.6512+120T>C
NM_000081.3:c.6081T>C , LRG_143t1:c.6081T>C	NP_000072.2:p.Val2027=
NM_001301365.1:c.6081T>C , LRG_143t2:c.6081T>C	NP_001288294.1:p.Val2027=
XM_011544031.1:c.6081T>C	XP_011542333.1:p.Val2027=
XM_011544032.1:c.6081T>C	XP_011542334.1:p.Val2027=
XM_011544033.1:c.6081T>C	XP_011542335.1:p.Val2027=
XM_011544034.1:c.5943T>C	XP_011542336.1:p.Val1981=
XM_011544035.1:c.6081T>C	XP_011542337.1:p.Val2027=
XM_011544036.1:c.3744T>C	XP_011542338.1:p.Val1248=
XM_011544037.1:c.6081T>C	XP_011542339.1:p.Val2027=
XM_011544038.1:c.6081T>C	XP_011542340.1:p.Val2027=
XM_011544039.1:c.6081T>C	XP_011542341.1:p.Val2027=
XM_011544040.1:c.5990T>C	XP_011542342.1:p.Phe1997Ser
XM_011544033.2:c.6081T>C	XP_011542335.1:p.Val2027=
XM_011544035.2:c.6081T>C	XP_011542337.1:p.Val2027=
XM_011544036.2:c.3744T>C	XP_011542338.1:p.Val1248=
XM_011544037.2:c.6081T>C	XP_011542339.1:p.Val2027=
XM_011544039.2:c.6081T>C	XP_011542341.1:p.Val2027=
XM_017000150.1:c.6081T>C	XP_016855639.1:p.Val2027=
XM_017000151.1:c.5852T>C	XP_016855640.1:p.Phe1951Ser
XR_001736946.2:n.6263T>C
XR_001736947.1:n.6263T>C
XR_001736948.1:n.6263T>C
XR_002959252.1:n.6172T>C
NM_000081.4:c.6081T>C MANE Select	NP_000072.2:p.Val2027=