Canonical Allele Identifier: CA10610396

Gene: LYST

Linked Data

• ClinVar Variation Id: 296321
• ClinVar RCV Id: RCV000400191
• dbSNP Id: rs886046156
• MyVariant Identifiers: chr1:g.235824802G>A (hg19) ; chr1:g.235661502G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235661502G>A , CM000663.2:g.235661502G>A	GRCh38
NC_000001.10:g.235824802G>A , CM000663.1:g.235824802G>A	GRCh37
NC_000001.9:g.233891425G>A	NCBI36
NG_007397.1:g.227139C>T , LRG_143:g.227139C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462376.2:n.4663C>T
ENST00000697178.1:c.*8830C>T	ENSP00000513163.1:n.*8830C>T
ENST00000697235.1:c.3394C>T	ENSP00000513202.1:n.3394C>T
ENST00000697236.1:c.6308C>T	ENSP00000513203.1:n.6308C>T
ENST00000697237.1:c.3555C>T
ENST00000389793.7:c.*1438C>T MANE Select	ENSP00000374443.2:n.*1438C>T
ENST00000389793.6:c.*1438C>T	ENSP00000374443.2:n.*1438C>T
ENST00000389794.7:c.*8205C>T	ENSP00000374444.4:n.*8205C>T
ENST00000473037.5:n.7834C>T
NM_000081.3:c.*1438C>T , LRG_143t1:c.*1438C>T	NP_000072.2:n.*1438C>T
NM_001301365.1:c.*1438C>T , LRG_143t2:c.*1438C>T	NP_001288294.1:n.*1438C>T
XM_011544031.1:c.*1438C>T	XP_011542333.1:n.*1438C>T
XM_011544032.1:c.*1438C>T	XP_011542334.1:n.*1438C>T
XM_011544033.1:c.*1438C>T	XP_011542335.1:n.*1438C>T
XM_011544034.1:c.*1438C>T	XP_011542336.1:n.*1438C>T
XM_011544036.1:c.*1438C>T	XP_011542338.1:n.*1438C>T
XM_011544033.2:c.*1438C>T	XP_011542335.1:n.*1438C>T
XM_011544036.2:c.*1438C>T	XP_011542338.1:n.*1438C>T
XM_017000150.1:c.*1438C>T	XP_016855639.1:n.*1438C>T
NM_000081.4:c.*1438C>T MANE Select	NP_000072.2:n.*1438C>T