Canonical Allele Identifier: CA1908795084
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI

Linked Data

dbSNP Id: rs1838310121

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49611950_49611951insTGTGT , CM000672.2:g.49611950_49611951insTGTGT GRCh38
NC_000010.10:g.50819996_50819997insTGTGT , CM000672.1:g.50819996_50819997insTGTGT GRCh37
NC_000010.9:g.50490002_50490003insTGTGT NCBI36
NG_011797.1:g.7856_7857insTGTGT
NG_053144.1:g.6650_6651insTGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000374115.5:c.1210_1211insTGTGT (SLC18A3) MANE Select ENSP00000363229.3:p.Thr404MetfsTer?
ENST00000339797.5:c.-69+2751_-69+2752insTGTGT (CHAT) ENSP00000343486.1:n.-69+2751_-69+2752insTGTGT
ENST00000374115.4:c.1210_1211insTGTGT (SLC18A3) ENSP00000363229.3:p.Thr404MetfsTer?
NM_003055.2:c.1210_1211insTGTGT (SLC18A3) NP_003046.2:p.Thr404MetfsTer?
NM_020984.3:c.-69+2751_-69+2752insTGTGT (CHAT) NP_066264.3:n.-69+2751_-69+2752insTGTGT
NM_003055.3:c.1210_1211insTGTGT (SLC18A3) MANE Select NP_003046.2:p.Thr404MetfsTer?
NM_020984.4:c.-69+2751_-69+2752insTGTGT (CHAT) NP_066264.4:n.-69+2751_-69+2752insTGTGT