gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00260033 (AFR)
Genomes Max Group AF
0.00228826 (AFR)
Exomes Max Group AF
0.00270489 (AFR)
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.4583071T>C , CM000671.2:g.4583071T>C | GRCh38 |
| NC_000009.11:g.4583071T>C , CM000671.1:g.4583071T>C | GRCh37 |
| NC_000009.10:g.4573071T>C | NCBI36 |
| NG_017044.1:g.97645T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262352.8:c.1227T>C (SLC1A1) MANE Select | ENSP00000262352.3:p.Ala409= | |
| ENST00000262352.7:c.1227T>C (SLC1A1) | ENSP00000262352.3:p.Ala409= | |
| ENST00000422398.1:c.481-2241T>C (SLC1A1) | ||
| ENST00000485616.5:c.*781+17582A>G (SPATA6L) | ENSP00000420003.1:n.*781+17582A>G | |
| NM_004170.5:c.1227T>C (SLC1A1) | NP_004161.4:p.Ala409= | |
| XM_011518007.1:c.1296T>C (SLC1A1) | XP_011516309.1:p.Ala432= | |
| XM_011518008.1:c.1236T>C (SLC1A1) | XP_011516310.1:p.Ala412= | |
| XM_011518009.1:c.1167T>C (SLC1A1) | XP_011516311.1:p.Ala389= | |
| XM_011518010.1:c.1086T>C (SLC1A1) | XP_011516312.1:p.Ala362= | |
| XM_011518008.3:c.1236T>C (SLC1A1) | XP_011516310.1:p.Ala412= | |
| XM_011518009.3:c.1167T>C (SLC1A1) | XP_011516311.1:p.Ala389= | |
| XM_017014882.2:c.*1+21108A>G (SPATA6L) | XP_016870371.1:n.*1+21108A>G | |
| XM_017015042.1:c.1188T>C (SLC1A1) | XP_016870531.1:p.Ala396= | |
| XM_017015043.1:c.1119T>C (SLC1A1) | XP_016870532.1:p.Ala373= | |
| XR_001746335.2:n.1478+17582A>G (SPATA6L) | ||
| NM_004170.6:c.1227T>C (SLC1A1) MANE Select | NP_004161.4:p.Ala409= |