Canonical Allele Identifier: CA2499219620
Gene: STXBP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1298371
ClinVar RCV Id: RCV001726701
dbSNP Id: rs2131472407

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127666167del , CM000671.2:g.127666167del GRCh38
NC_000009.11:g.130428446del , CM000671.1:g.130428446del GRCh37
NC_000009.10:g.129468267del NCBI36
NG_016623.1:g.58961del

Transcript Alleles

HGVS Amino-acid change
ENST00000704680.1:c.623del
ENST00000704681.1:c.665del
ENST00000373299.5:c.665del
ENST00000373302.8:c.665del
ENST00000626539.3:c.623del
ENST00000635950.2:c.665del
ENST00000636509.2:c.623del
ENST00000636962.2:c.665del
ENST00000637060.2:c.*307del
ENST00000637173.2:c.623del
ENST00000637464.2:c.*1529del
ENST00000637521.2:c.623del
ENST00000637953.1:c.665del
ENST00000647107.1:c.607del
ENST00000650920.1:c.623del
ENST00000373299.4:c.665del
ENST00000373302.7:c.665del
ENST00000626416.2:n.501del
NM_001032221.3:c.665del
NM_003165.3:c.665del
NM_001032221.6:c.665del
NM_001374306.2:c.656del
NM_001374307.2:c.623del
NM_001374308.2:c.623del
NM_001374309.2:c.623del
NM_001374310.2:c.623del
NM_001374311.2:c.623del
NM_001374312.2:c.623del
NM_001374313.2:c.665del
NM_001374314.1:c.665del
NM_001374315.2:c.665del
NM_003165.6:c.665del