Canonical Allele Identifier: CA2574545085
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49611305_49611309del , CM000672.2:g.49611305_49611309del GRCh38
NC_000010.10:g.50819351_50819355del , CM000672.1:g.50819351_50819355del GRCh37
NC_000010.9:g.50489357_50489361del NCBI36
NG_011797.1:g.7211_7215del
NG_053144.1:g.6005_6009del

Transcript Alleles

HGVS Amino-acid change
ENST00000374115.5:c.565_569del (SLC18A3) MANE Select ENSP00000363229.3:p.Ser189LeufsTer13
ENST00000339797.5:c.-69+2106_-69+2110del (CHAT) ENSP00000343486.1:n.-69+2106_-69+2110del
ENST00000374115.4:c.565_569del (SLC18A3) ENSP00000363229.3:p.Ser189LeufsTer13
NM_003055.2:c.565_569del (SLC18A3) NP_003046.2:p.Ser189LeufsTer13
NM_020984.3:c.-69+2106_-69+2110del (CHAT) NP_066264.3:n.-69+2106_-69+2110del
NM_003055.3:c.565_569del (SLC18A3) MANE Select NP_003046.2:p.Ser189LeufsTer13
NM_020984.4:c.-69+2106_-69+2110del (CHAT) NP_066264.4:n.-69+2106_-69+2110del