Canonical Allele Identifier: CA376721867
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI

Linked Data

ClinVar Variation Id: 2321548
ClinVar RCV Id: RCV002915675
dbSNP Id: rs1590545082

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49611773A>G , CM000672.2:g.49611773A>G GRCh38
NC_000010.10:g.50819819A>G , CM000672.1:g.50819819A>G GRCh37
NC_000010.9:g.50489825A>G NCBI36
NG_011797.1:g.7679A>G
NG_053144.1:g.6473A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374115.5:c.1033A>G (SLC18A3) MANE Select ENSP00000363229.3:p.Thr345Ala
ENST00000339797.5:c.-69+2574A>G (CHAT) ENSP00000343486.1:n.-69+2574A>G
ENST00000374115.4:c.1033A>G (SLC18A3) ENSP00000363229.3:p.Thr345Ala
NM_003055.2:c.1033A>G (SLC18A3) NP_003046.2:p.Thr345Ala
NM_020984.3:c.-69+2574A>G (CHAT) NP_066264.3:n.-69+2574A>G
NM_003055.3:c.1033A>G (SLC18A3) MANE Select NP_003046.2:p.Thr345Ala
NM_020984.4:c.-69+2574A>G (CHAT) NP_066264.4:n.-69+2574A>G