Canonical Allele Identifier: CA529585311
Gene: LYST HGNC NCBI
ClinVar RCV:
ClinVar Variation:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235663095A>G , CM000663.2:g.235663095A>G GRCh38
NC_000001.10:g.235826395A>G , CM000663.1:g.235826395A>G GRCh37
NC_000001.9:g.233893018A>G NCBI36
NG_007397.1:g.225546T>C , LRG_143:g.225546T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000462376.2:n.3087-17T>C
ENST00000697178.1:c.*7254-17T>C ENSP00000513163.1:n.*7254-17T>C
ENST00000697235.1:c.1818-17T>C ENSP00000513202.1:n.1818-17T>C
ENST00000697236.1:c.4732-17T>C ENSP00000513203.1:n.4732-17T>C
ENST00000697237.1:c.1979-17T>C
ENST00000697238.1:n.422-17T>C
ENST00000697239.1:n.662-17T>C
ENST00000697240.1:c.3335-17T>C ENSP00000513205.1:n.3335-17T>C
ENST00000389793.7:c.11268-17T>C MANE Select ENSP00000374443.2:n.11268-17T>C
ENST00000389793.6:c.11268-17T>C ENSP00000374443.2:n.11268-17T>C
ENST00000389794.7:c.*6692-17T>C ENSP00000374444.4:n.*6692-17T>C
ENST00000473037.5:n.6258-17T>C
NM_000081.3:c.11268-17T>C , LRG_143t1:c.11268-17T>C NP_000072.2:n.11268-17T>C
NM_001301365.1:c.11268-17T>C , LRG_143t2:c.11268-17T>C NP_001288294.1:n.11268-17T>C
XM_011544031.1:c.11430-17T>C XP_011542333.1:n.11430-17T>C
XM_011544032.1:c.11430-17T>C XP_011542334.1:n.11430-17T>C
XM_011544033.1:c.11430-17T>C XP_011542335.1:n.11430-17T>C
XM_011544034.1:c.11292-17T>C XP_011542336.1:n.11292-17T>C
XM_011544036.1:c.9093-17T>C XP_011542338.1:n.9093-17T>C
XM_011544033.2:c.11430-17T>C XP_011542335.1:n.11430-17T>C
XM_011544036.2:c.9093-17T>C XP_011542338.1:n.9093-17T>C
XM_017000150.1:c.11199-17T>C XP_016855639.1:n.11199-17T>C
NM_000081.4:c.11268-17T>C MANE Select NP_000072.2:n.11268-17T>C