Linked Data
ClinVar Variation Id:
298416
dbSNP Id:
rs79410539
ExAC:
10:101486711 T / C
gnomAD v2:
10-101486711-T-C
gnomAD v3:
10-99726954-T-C
gnomAD v4:
10-99726954-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99726954T>C , CM000672.2:g.99726954T>C | GRCh38 |
| NC_000010.10:g.101486711T>C , CM000672.1:g.101486711T>C | GRCh37 |
| NC_000010.9:g.101476701T>C | NCBI36 |
| NG_008986.1:g.10713A>G , LRG_406:g.10713A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000016171.6:c.582+14A>G (COX15) MANE Select | ENSP00000016171.6:n.582+14A>G | |
| ENST00000649102.1:c.499+14A>G | ENSP00000497114.1:n.499+14A>G | |
| ENST00000016171.5:c.582+14A>G (COX15) | ENSP00000016171.5:n.582+14A>G | |
| ENST00000370483.9:c.582+14A>G (COX15) | ENSP00000359514.5:n.582+14A>G | |
| ENST00000493385.5:n.309+3844T>C (CUTC) | ||
| NM_004376.5:c.582+14A>G , LRG_406t2:c.582+14A>G (COX15) | NP_004367.2:n.582+14A>G | |
| NM_078470.4:c.582+14A>G , LRG_406t1:c.582+14A>G (COX15) | NP_510870.1:n.582+14A>G | |
| XM_005269539.3:c.582+14A>G (COX15) | XP_005269596.1:n.582+14A>G | |
| XM_006717633.2:c.582+14A>G (COX15) | XP_006717696.1:n.582+14A>G | |
| XM_006717634.2:c.582+14A>G (COX15) | XP_006717697.1:n.582+14A>G | |
| XM_011539298.1:c.582+14A>G (COX15) | XP_011537600.1:n.582+14A>G | |
| NM_001320974.1:c.582+14A>G (COX15) | NP_001307903.1:n.582+14A>G | |
| NM_001320975.1:c.582+14A>G (COX15) | NP_001307904.1:n.582+14A>G | |
| NM_001320976.1:c.45+14A>G (COX15) | NP_001307905.1:n.45+14A>G | |
| NM_004376.6:c.582+14A>G (COX15) | NP_004367.2:n.582+14A>G | |
| NM_078470.5:c.582+14A>G (COX15) | NP_510870.1:n.582+14A>G | |
| XM_006717634.3:c.582+14A>G (COX15) | XP_006717697.1:n.582+14A>G | |
| XM_011539298.2:c.582+14A>G (COX15) | XP_011537600.1:n.582+14A>G | |
| NM_001320974.2:c.582+14A>G (COX15) | NP_001307903.1:n.582+14A>G | |
| NM_001320975.2:c.582+14A>G (COX15) | NP_001307904.1:n.582+14A>G | |
| NM_001320976.2:c.45+14A>G (COX15) | NP_001307905.1:n.45+14A>G | |
| NM_001372024.1:c.582+14A>G (COX15) | NP_001358953.1:n.582+14A>G | |
| NM_001372025.1:c.582+14A>G (COX15) | NP_001358954.1:n.582+14A>G | |
| NM_001372026.1:c.582+14A>G (COX15) | NP_001358955.1:n.582+14A>G | |
| NM_001372027.1:c.582+14A>G (COX15) | NP_001358956.1:n.582+14A>G | |
| NM_001372028.1:c.582+14A>G (COX15) | NP_001358957.1:n.582+14A>G | |
| NM_004376.7:c.582+14A>G (COX15) | NP_004367.2:n.582+14A>G | |
| NM_078470.6:c.582+14A>G (COX15) MANE Select | NP_510870.1:n.582+14A>G | |
| NR_164009.1:n.577+14A>G (COX15) |