Canonical Allele Identifier: CA1908793138
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49611201C= , CM000672.2:g.49611201C= GRCh38
NC_000010.10:g.50819247C= , CM000672.1:g.50819247C= GRCh37
NC_000010.9:g.50489253C= NCBI36
NG_011797.1:g.7107C=
NG_053144.1:g.5901C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374115.5:c.461C= (SLC18A3) MANE Select ENSP00000363229.3:p.Pro154=
ENST00000339797.5:c.-69+2002C= (CHAT) ENSP00000343486.1:n.-69+2002C=
ENST00000374115.4:c.461C= (SLC18A3) ENSP00000363229.3:p.Pro154=
NM_003055.2:c.461C= (SLC18A3) NP_003046.2:p.Pro154=
NM_020984.3:c.-69+2002C= (CHAT) NP_066264.3:n.-69+2002C=
NM_003055.3:c.461C= (SLC18A3) MANE Select NP_003046.2:p.Pro154=
NM_020984.4:c.-69+2002C= (CHAT) NP_066264.4:n.-69+2002C=