Canonical Allele Identifier: CA344957050

Gene: LYST

Linked Data

• ClinVar Variation Id: 1386180
• ClinVar RCV Id: RCV001905710
• MyVariant Identifiers: chr1:g.235969958G>C (hg19) ; chr1:g.235806658G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235806658G>C , CM000663.2:g.235806658G>C	GRCh38
NC_000001.10:g.235969958G>C , CM000663.1:g.235969958G>C	GRCh37
NC_000001.9:g.234036581G>C	NCBI36
NG_007397.1:g.81983C>G , LRG_143:g.81983C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697178.1:c.2478C>G	ENSP00000513163.1:p.Ser826Arg
ENST00000697242.1:c.1881C>G	ENSP00000513207.1:p.Ser627Arg
ENST00000389793.7:c.2478C>G MANE Select	ENSP00000374443.2:p.Ser826Arg
ENST00000389793.6:c.2478C>G	ENSP00000374443.2:p.Ser826Arg
ENST00000389794.7:c.2478C>G	ENSP00000374444.4:p.Ser826Arg
ENST00000465349.5:n.3029C>G
ENST00000489585.5:n.3029C>G
NM_000081.3:c.2478C>G , LRG_143t1:c.2478C>G	NP_000072.2:p.Ser826Arg
NM_001301365.1:c.2478C>G , LRG_143t2:c.2478C>G	NP_001288294.1:p.Ser826Arg
XM_011544031.1:c.2478C>G	XP_011542333.1:p.Ser826Arg
XM_011544032.1:c.2478C>G	XP_011542334.1:p.Ser826Arg
XM_011544033.1:c.2478C>G	XP_011542335.1:p.Ser826Arg
XM_011544034.1:c.2478C>G	XP_011542336.1:p.Ser826Arg
XM_011544035.1:c.2478C>G	XP_011542337.1:p.Ser826Arg
XM_011544036.1:c.141C>G	XP_011542338.1:p.Ser47Arg
XM_011544037.1:c.2478C>G	XP_011542339.1:p.Ser826Arg
XM_011544038.1:c.2478C>G	XP_011542340.1:p.Ser826Arg
XM_011544039.1:c.2478C>G	XP_011542341.1:p.Ser826Arg
XM_011544040.1:c.2478C>G	XP_011542342.1:p.Ser826Arg
XM_011544033.2:c.2478C>G	XP_011542335.1:p.Ser826Arg
XM_011544035.2:c.2478C>G	XP_011542337.1:p.Ser826Arg
XM_011544036.2:c.141C>G	XP_011542338.1:p.Ser47Arg
XM_011544037.2:c.2478C>G	XP_011542339.1:p.Ser826Arg
XM_011544039.2:c.2478C>G	XP_011542341.1:p.Ser826Arg
XM_017000150.1:c.2478C>G	XP_016855639.1:p.Ser826Arg
XM_017000151.1:c.2478C>G	XP_016855640.1:p.Ser826Arg
XR_001736946.2:n.2660C>G
XR_001736947.1:n.2660C>G
XR_001736948.1:n.2660C>G
XR_002959252.1:n.2660C>G
NM_000081.4:c.2478C>G MANE Select	NP_000072.2:p.Ser826Arg