Canonical Allele Identifier: CA2637004458
Gene: SLC6A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221467_30221490del , CM000679.2:g.30221467_30221490del GRCh38
NC_000017.10:g.28548485_28548508del , CM000679.1:g.28548485_28548508del GRCh37
NC_000017.9:g.25572611_25572634del NCBI36
NG_011747.2:g.19447_19470del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+126_343+149del MANE Select ENSP00000498537.1:n.343+126_343+149del
ENST00000261707.7:c.343+126_343+149del ENSP00000261707.3:n.343+126_343+149del
ENST00000394821.2:c.343+126_343+149del ENSP00000378298.2:n.343+126_343+149del
ENST00000401766.6:c.343+126_343+149del ENSP00000385822.2:n.343+126_343+149del
NM_001045.5:c.343+126_343+149del NP_001036.1:n.343+126_343+149del
NM_001045.6:c.343+126_343+149del MANE Select NP_001036.1:n.343+126_343+149del