Canonical Allele Identifier: CA289281462
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs71361447

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221459_30221479delinsTCCCA , CM000679.2:g.30221459_30221479delinsTCCCA GRCh38
NC_000017.10:g.28548477_28548497delinsTCCCA , CM000679.1:g.28548477_28548497delinsTCCCA GRCh37
NC_000017.9:g.25572603_25572623delinsTCCCA NCBI36
NG_011747.2:g.19458_19478delinsTGGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+137_343+157delinsTGGGA MANE Select ENSP00000498537.1:n.343+137_343+157delinsTGGGA
ENST00000261707.7:c.343+137_343+157delinsTGGGA ENSP00000261707.3:n.343+137_343+157delinsTGGGA
ENST00000394821.2:c.343+137_343+157delinsTGGGA ENSP00000378298.2:n.343+137_343+157delinsTGGGA
ENST00000401766.6:c.343+137_343+157delinsTGGGA ENSP00000385822.2:n.343+137_343+157delinsTGGGA
NM_001045.5:c.343+137_343+157delinsTGGGA NP_001036.1:n.343+137_343+157delinsTGGGA
NM_001045.6:c.343+137_343+157delinsTGGGA MANE Select NP_001036.1:n.343+137_343+157delinsTGGGA