Canonical Allele Identifier: CA2255095490
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906883079

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224845_30224848dup , CM000679.2:g.30224845_30224848dup GRCh38
NC_000017.10:g.28551863_28551866dup , CM000679.1:g.28551863_28551866dup GRCh37
NC_000017.9:g.25575989_25575992dup NCBI36
NG_011747.2:g.16089_16092dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-1933_-220-1930dup MANE Select ENSP00000498537.1:n.-220-1933_-220-1930dup
ENST00000261707.7:c.-220-1933_-220-1930dup ENSP00000261707.3:n.-220-1933_-220-1930dup
ENST00000394821.2:c.-220-1933_-220-1930dup ENSP00000378298.2:n.-220-1933_-220-1930dup
ENST00000401766.6:c.-123-2767_-123-2764dup ENSP00000385822.2:n.-123-2767_-123-2764dup
NM_001045.5:c.-220-1933_-220-1930dup NP_001036.1:n.-220-1933_-220-1930dup
NM_001045.6:c.-220-1933_-220-1930dup MANE Select NP_001036.1:n.-220-1933_-220-1930dup