Linked Data
gnomAD v4:
X-153688603-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153688603T>C , CM000685.2:g.153688603T>C | GRCh38 |
| NC_000023.10:g.152954058T>C , CM000685.1:g.152954058T>C | GRCh37 |
| NC_000023.9:g.152607252T>C | NCBI36 |
| NG_012016.1:g.5307T>C | |
| NG_012016.2:g.5307T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.29T>C (SLC6A8) MANE Select | ENSP00000253122.5:p.Ile10Thr | |
| ENST00000253122.9:c.29T>C (SLC6A8) | ENSP00000253122.5:p.Ile10Thr | |
| ENST00000458354.5:c.-3+212A>G (PNCK) | ENSP00000401542.1:n.-3+212A>G | |
| ENST00000480693.1:n.64+212A>G (PNCK) | ||
| NM_001142805.1:c.29T>C (SLC6A8) | NP_001136277.1:p.Ile10Thr | |
| NM_005629.3:c.29T>C (SLC6A8) | NP_005620.1:p.Ile10Thr | |
| NM_005629.4:c.29T>C (SLC6A8) MANE Select | NP_005620.1:p.Ile10Thr | |
| NM_001142805.2:c.29T>C (SLC6A8) | NP_001136277.1:p.Ile10Thr |