Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153688925C= , CM000685.2:g.153688925C= | GRCh38 |
| NC_000023.10:g.152954380C= , CM000685.1:g.152954380C= | GRCh37 |
| NC_000023.9:g.152607574C= | NCBI36 |
| NG_012016.1:g.5629C= | |
| NG_012016.2:g.5629C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.262+89C= (SLC6A8) MANE Select | ENSP00000253122.5:n.262+89C= | |
| ENST00000253122.9:c.262+89C= (SLC6A8) | ENSP00000253122.5:n.262+89C= | |
| ENST00000458354.5:c.-113G= (PNCK) | ENSP00000401542.1:n.-113G= | |
| ENST00000476466.1:n.114+89C= (SLC6A8) | ||
| NM_001142805.1:c.262+89C= (SLC6A8) | NP_001136277.1:n.262+89C= | |
| NM_005629.3:c.262+89C= (SLC6A8) | NP_005620.1:n.262+89C= | |
| NM_005629.4:c.262+89C= (SLC6A8) MANE Select | NP_005620.1:n.262+89C= | |
| NM_001142805.2:c.262+89C= (SLC6A8) | NP_001136277.1:n.262+89C= |