Canonical Allele Identifier: CA2255093992
Gene: SLC6A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30221458_30221459delinsAC , CM000679.2:g.30221458_30221459delinsAC GRCh38
NC_000017.10:g.28548476_28548477delinsAC , CM000679.1:g.28548476_28548477delinsAC GRCh37
NC_000017.9:g.25572602_25572603delinsAC NCBI36
NG_011747.2:g.19478_19479delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.343+157_343+158delinsGT MANE Select ENSP00000498537.1:n.343+157_343+158delinsGT
ENST00000261707.7:c.343+157_343+158delinsGT ENSP00000261707.3:n.343+157_343+158delinsGT
ENST00000394821.2:c.343+157_343+158delinsGT ENSP00000378298.2:n.343+157_343+158delinsGT
ENST00000401766.6:c.343+157_343+158delinsGT ENSP00000385822.2:n.343+157_343+158delinsGT
NM_001045.5:c.343+157_343+158delinsGT NP_001036.1:n.343+157_343+158delinsGT
NM_001045.6:c.343+157_343+158delinsGT MANE Select NP_001036.1:n.343+157_343+158delinsGT