Canonical Allele Identifier: CA376718262
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.50819140G>C (hg19) chr10:g.49611094G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49611094G>C , CM000672.2:g.49611094G>C GRCh38
NC_000010.10:g.50819140G>C , CM000672.1:g.50819140G>C GRCh37
NC_000010.9:g.50489146G>C NCBI36
NG_011797.1:g.7000G>C
NG_053144.1:g.5794G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374115.5:c.354G>C (SLC18A3) MANE Select ENSP00000363229.3:p.Glu118Asp
ENST00000339797.5:c.-69+1895G>C (CHAT) ENSP00000343486.1:n.-69+1895G>C
ENST00000374115.4:c.354G>C (SLC18A3) ENSP00000363229.3:p.Glu118Asp
NM_003055.2:c.354G>C (SLC18A3) NP_003046.2:p.Glu118Asp
NM_020984.3:c.-69+1895G>C (CHAT) NP_066264.3:n.-69+1895G>C
NM_003055.3:c.354G>C (SLC18A3) MANE Select NP_003046.2:p.Glu118Asp
NM_020984.4:c.-69+1895G>C (CHAT) NP_066264.4:n.-69+1895G>C
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