Canonical Allele Identifier: CA2609116660
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49611685_49611688del , CM000672.2:g.49611685_49611688del GRCh38
NC_000010.10:g.50819731_50819734del , CM000672.1:g.50819731_50819734del GRCh37
NC_000010.9:g.50489737_50489740del NCBI36
NG_011797.1:g.7591_7594del
NG_053144.1:g.6385_6388del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374115.5:c.945_948del (SLC18A3) MANE Select ENSP00000363229.3:p.Trp315Ter
ENST00000339797.5:c.-69+2486_-69+2489del (CHAT) ENSP00000343486.1:n.-69+2486_-69+2489del
ENST00000374115.4:c.945_948del (SLC18A3) ENSP00000363229.3:p.Trp315Ter
NM_003055.2:c.945_948del (SLC18A3) NP_003046.2:p.Trp315Ter
NM_020984.3:c.-69+2486_-69+2489del (CHAT) NP_066264.3:n.-69+2486_-69+2489del
NM_003055.3:c.945_948del (SLC18A3) MANE Select NP_003046.2:p.Trp315Ter
NM_020984.4:c.-69+2486_-69+2489del (CHAT) NP_066264.4:n.-69+2486_-69+2489del