Canonical Allele Identifier: CA10609524

Gene: LYST

Linked Data

• ClinVar Variation Id: 296334
• ClinVar RCV Id: RCV000322911
• dbSNP Id: rs886046162
• MyVariant Identifiers: chr1:g.235825546A>G (hg19) ; chr1:g.235662246A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235662246A>G , CM000663.2:g.235662246A>G	GRCh38
NC_000001.10:g.235825546A>G , CM000663.1:g.235825546A>G	GRCh37
NC_000001.9:g.233892169A>G	NCBI36
NG_007397.1:g.226395T>C , LRG_143:g.226395T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000462376.2:n.3919T>C
ENST00000697178.1:c.*8086T>C	ENSP00000513163.1:n.*8086T>C
ENST00000697235.1:c.2650T>C	ENSP00000513202.1:n.2650T>C
ENST00000697236.1:c.5564T>C	ENSP00000513203.1:n.5564T>C
ENST00000697237.1:c.2811T>C
ENST00000389793.7:c.*694T>C MANE Select	ENSP00000374443.2:n.*694T>C
ENST00000389793.6:c.*694T>C	ENSP00000374443.2:n.*694T>C
ENST00000389794.7:c.*7524T>C	ENSP00000374444.4:n.*7524T>C
ENST00000473037.5:n.7090T>C
NM_000081.3:c.*694T>C , LRG_143t1:c.*694T>C	NP_000072.2:n.*694T>C
NM_001301365.1:c.*694T>C , LRG_143t2:c.*694T>C	NP_001288294.1:n.*694T>C
XM_011544031.1:c.*694T>C	XP_011542333.1:n.*694T>C
XM_011544032.1:c.*694T>C	XP_011542334.1:n.*694T>C
XM_011544033.1:c.*694T>C	XP_011542335.1:n.*694T>C
XM_011544034.1:c.*694T>C	XP_011542336.1:n.*694T>C
XM_011544036.1:c.*694T>C	XP_011542338.1:n.*694T>C
XM_011544033.2:c.*694T>C	XP_011542335.1:n.*694T>C
XM_011544036.2:c.*694T>C	XP_011542338.1:n.*694T>C
XM_017000150.1:c.*694T>C	XP_016855639.1:n.*694T>C
NM_000081.4:c.*694T>C MANE Select	NP_000072.2:n.*694T>C