Canonical Allele Identifier: CA376716176
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.50818943A>T (hg19) chr10:g.49610897A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49610897A>T , CM000672.2:g.49610897A>T GRCh38
NC_000010.10:g.50818943A>T , CM000672.1:g.50818943A>T GRCh37
NC_000010.9:g.50488949A>T NCBI36
NG_011797.1:g.6803A>T
NG_053144.1:g.5597A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374115.5:c.157A>T (SLC18A3) MANE Select ENSP00000363229.3:p.Ile53Phe
ENST00000339797.5:c.-69+1698A>T (CHAT) ENSP00000343486.1:n.-69+1698A>T
ENST00000374115.4:c.157A>T (SLC18A3) ENSP00000363229.3:p.Ile53Phe
NM_003055.2:c.157A>T (SLC18A3) NP_003046.2:p.Ile53Phe
NM_020984.3:c.-69+1698A>T (CHAT) NP_066264.3:n.-69+1698A>T
NM_003055.3:c.157A>T (SLC18A3) MANE Select NP_003046.2:p.Ile53Phe
NM_020984.4:c.-69+1698A>T (CHAT) NP_066264.4:n.-69+1698A>T
Search 100 bp 5'
Search 100 bp 3'