Canonical Allele Identifier: CA2636978330
Gene: SLC6A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221557_30221559del , CM000679.2:g.30221557_30221559del GRCh38
NC_000017.10:g.28548575_28548577del , CM000679.1:g.28548575_28548577del GRCh37
NC_000017.9:g.25572701_25572703del NCBI36
NG_011747.2:g.19379_19381del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+58_343+60del MANE Select ENSP00000498537.1:n.343+58_343+60del
ENST00000261707.7:c.343+58_343+60del ENSP00000261707.3:n.343+58_343+60del
ENST00000394821.2:c.343+58_343+60del ENSP00000378298.2:n.343+58_343+60del
ENST00000401766.6:c.343+58_343+60del ENSP00000385822.2:n.343+58_343+60del
NM_001045.5:c.343+58_343+60del NP_001036.1:n.343+58_343+60del
NM_001045.6:c.343+58_343+60del MANE Select NP_001036.1:n.343+58_343+60del