Canonical Allele Identifier: CA10610400

Gene: LYST

Linked Data

• ClinVar Variation Id: 296328
• ClinVar RCV Id: RCV000310955
• dbSNP Id: rs886046159
• MyVariant Identifiers: chr1:g.235825333C>T (hg19) ; chr1:g.235662033C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235662033C>T , CM000663.2:g.235662033C>T	GRCh38
NC_000001.10:g.235825333C>T , CM000663.1:g.235825333C>T	GRCh37
NC_000001.9:g.233891956C>T	NCBI36
NG_007397.1:g.226608G>A , LRG_143:g.226608G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462376.2:n.4132G>A
ENST00000697178.1:c.*8299G>A	ENSP00000513163.1:n.*8299G>A
ENST00000697235.1:c.2863G>A	ENSP00000513202.1:n.2863G>A
ENST00000697236.1:c.5777G>A	ENSP00000513203.1:n.5777G>A
ENST00000697237.1:c.3024G>A
ENST00000389793.7:c.*907G>A MANE Select	ENSP00000374443.2:n.*907G>A
ENST00000389793.6:c.*907G>A	ENSP00000374443.2:n.*907G>A
ENST00000389794.7:c.*7737G>A	ENSP00000374444.4:n.*7737G>A
ENST00000473037.5:n.7303G>A
NM_000081.3:c.*907G>A , LRG_143t1:c.*907G>A	NP_000072.2:n.*907G>A
NM_001301365.1:c.*907G>A , LRG_143t2:c.*907G>A	NP_001288294.1:n.*907G>A
XM_011544031.1:c.*907G>A	XP_011542333.1:n.*907G>A
XM_011544032.1:c.*907G>A	XP_011542334.1:n.*907G>A
XM_011544033.1:c.*907G>A	XP_011542335.1:n.*907G>A
XM_011544034.1:c.*907G>A	XP_011542336.1:n.*907G>A
XM_011544036.1:c.*907G>A	XP_011542338.1:n.*907G>A
XM_011544033.2:c.*907G>A	XP_011542335.1:n.*907G>A
XM_011544036.2:c.*907G>A	XP_011542338.1:n.*907G>A
XM_017000150.1:c.*907G>A	XP_016855639.1:n.*907G>A
NM_000081.4:c.*907G>A MANE Select	NP_000072.2:n.*907G>A