Canonical Allele Identifier: CA2255095581
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906888249

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30225083_30225089del , CM000679.2:g.30225083_30225089del GRCh38
NC_000017.10:g.28552101_28552107del , CM000679.1:g.28552101_28552107del GRCh37
NC_000017.9:g.25576227_25576233del NCBI36
NG_011747.2:g.15850_15856del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-2172_-220-2166del MANE Select ENSP00000498537.1:n.-220-2172_-220-2166del
ENST00000261707.7:c.-220-2172_-220-2166del ENSP00000261707.3:n.-220-2172_-220-2166del
ENST00000394821.2:c.-220-2172_-220-2166del ENSP00000378298.2:n.-220-2172_-220-2166del
ENST00000401766.6:c.-123-3006_-123-3000del ENSP00000385822.2:n.-123-3006_-123-3000del
NM_001045.5:c.-220-2172_-220-2166del NP_001036.1:n.-220-2172_-220-2166del
NM_001045.6:c.-220-2172_-220-2166del MANE Select NP_001036.1:n.-220-2172_-220-2166del