Canonical Allele Identifier: CA376716034
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.50818926A>C (hg19) chr10:g.49610880A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49610880A>C , CM000672.2:g.49610880A>C GRCh38
NC_000010.10:g.50818926A>C , CM000672.1:g.50818926A>C GRCh37
NC_000010.9:g.50488932A>C NCBI36
NG_011797.1:g.6786A>C
NG_053144.1:g.5580A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374115.5:c.140A>C (SLC18A3) MANE Select ENSP00000363229.3:p.Asn47Thr
ENST00000339797.5:c.-69+1681A>C (CHAT) ENSP00000343486.1:n.-69+1681A>C
ENST00000374115.4:c.140A>C (SLC18A3) ENSP00000363229.3:p.Asn47Thr
NM_003055.2:c.140A>C (SLC18A3) NP_003046.2:p.Asn47Thr
NM_020984.3:c.-69+1681A>C (CHAT) NP_066264.3:n.-69+1681A>C
NM_003055.3:c.140A>C (SLC18A3) MANE Select NP_003046.2:p.Asn47Thr
NM_020984.4:c.-69+1681A>C (CHAT) NP_066264.4:n.-69+1681A>C
Search 100 bp 5'
Search 100 bp 3'