Canonical Allele Identifier: CA2609117487
Gene: SLC18A3 HGNC NCBI
CHAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49611984_49611985del , CM000672.2:g.49611984_49611985del GRCh38
NC_000010.10:g.50820030_50820031del , CM000672.1:g.50820030_50820031del GRCh37
NC_000010.9:g.50490036_50490037del NCBI36
NG_011797.1:g.7890_7891del
NG_053144.1:g.6684_6685del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374115.5:c.1244_1245del (SLC18A3) MANE Select ENSP00000363229.3:p.Ser415CysfsTer?
ENST00000339797.5:c.-69+2785_-69+2786del (CHAT) ENSP00000343486.1:n.-69+2785_-69+2786del
ENST00000374115.4:c.1244_1245del (SLC18A3) ENSP00000363229.3:p.Ser415CysfsTer?
NM_003055.2:c.1244_1245del (SLC18A3) NP_003046.2:p.Ser415CysfsTer?
NM_020984.3:c.-69+2785_-69+2786del (CHAT) NP_066264.3:n.-69+2785_-69+2786del
NM_003055.3:c.1244_1245del (SLC18A3) MANE Select NP_003046.2:p.Ser415CysfsTer?
NM_020984.4:c.-69+2785_-69+2786del (CHAT) NP_066264.4:n.-69+2785_-69+2786del