Linked Data
ClinVar Variation Id:
1464132
ClinVar RCV Id:
RCV001997882
dbSNP Id:
rs1295513059
gnomAD v4:
X-153688646-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153688646G>T , CM000685.2:g.153688646G>T | GRCh38 |
| NC_000023.10:g.152954101G>T , CM000685.1:g.152954101G>T | GRCh37 |
| NC_000023.9:g.152607295G>T | NCBI36 |
| NG_012016.1:g.5350G>T | |
| NG_012016.2:g.5350G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.72G>T (SLC6A8) MANE Select | ENSP00000253122.5:p.Ala24= | |
| ENST00000253122.9:c.72G>T (SLC6A8) | ENSP00000253122.5:p.Ala24= | |
| ENST00000458354.5:c.-3+169C>A (PNCK) | ENSP00000401542.1:n.-3+169C>A | |
| ENST00000480693.1:n.64+169C>A (PNCK) | ||
| NM_001142805.1:c.72G>T (SLC6A8) | NP_001136277.1:p.Ala24= | |
| NM_005629.3:c.72G>T (SLC6A8) | NP_005620.1:p.Ala24= | |
| NM_005629.4:c.72G>T (SLC6A8) MANE Select | NP_005620.1:p.Ala24= | |
| NM_001142805.2:c.72G>T (SLC6A8) | NP_001136277.1:p.Ala24= |