Canonical Allele Identifier: CA1908794962
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49611894T= , CM000672.2:g.49611894T= GRCh38
NC_000010.10:g.50819940T= , CM000672.1:g.50819940T= GRCh37
NC_000010.9:g.50489946T= NCBI36
NG_011797.1:g.7800T=
NG_053144.1:g.6594T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374115.5:c.1154T= (SLC18A3) MANE Select ENSP00000363229.3:p.Val385=
ENST00000339797.5:c.-69+2695T= (CHAT) ENSP00000343486.1:n.-69+2695T=
ENST00000374115.4:c.1154T= (SLC18A3) ENSP00000363229.3:p.Val385=
NM_003055.2:c.1154T= (SLC18A3) NP_003046.2:p.Val385=
NM_020984.3:c.-69+2695T= (CHAT) NP_066264.3:n.-69+2695T=
NM_003055.3:c.1154T= (SLC18A3) MANE Select NP_003046.2:p.Val385=
NM_020984.4:c.-69+2695T= (CHAT) NP_066264.4:n.-69+2695T=
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