Canonical Allele Identifier: CA2255095497
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1906883404

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224874_30224897del , CM000679.2:g.30224874_30224897del GRCh38
NC_000017.10:g.28551892_28551915del , CM000679.1:g.28551892_28551915del GRCh37
NC_000017.9:g.25576018_25576041del NCBI36
NG_011747.2:g.16042_16065del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-1980_-220-1957del MANE Select ENSP00000498537.1:n.-220-1980_-220-1957del
ENST00000261707.7:c.-220-1980_-220-1957del ENSP00000261707.3:n.-220-1980_-220-1957del
ENST00000394821.2:c.-220-1980_-220-1957del ENSP00000378298.2:n.-220-1980_-220-1957del
ENST00000401766.6:c.-123-2814_-123-2791del ENSP00000385822.2:n.-123-2814_-123-2791del
NM_001045.5:c.-220-1980_-220-1957del NP_001036.1:n.-220-1980_-220-1957del
NM_001045.6:c.-220-1980_-220-1957del MANE Select NP_001036.1:n.-220-1980_-220-1957del