Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.24882947A= , CM000675.2:g.24882947A= | GRCh38 |
| NC_000013.10:g.25457085A= , CM000675.1:g.25457085A= | GRCh37 |
| NC_000013.9:g.24355085A= | NCBI36 |
| NG_009165.2:g.45001T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381884.9:c.*230T= (CENPJ) MANE Select | ENSP00000371308.4:n.*230T= | |
| ENST00000616936.4:c.*901T= (CENPJ) | ENSP00000477511.1:n.*901T= | |
| NM_018451.4:c.*230T= (CENPJ) | NP_060921.3:n.*230T= | |
| NR_047594.1:n.4559T= (CENPJ) | ||
| NR_047595.1:n.4357T= (CENPJ) | ||
| XM_011535156.1:c.*10+3652A= (RNF17) | XP_011533458.1:n.*10+3652A= | |
| XM_011535156.2:c.*10+3652A= (RNF17) | XP_011533458.1:n.*10+3652A= | |
| NM_018451.5:c.*230T= (CENPJ) MANE Select | NP_060921.3:n.*230T= | |
| NR_047594.2:n.4531T= (CENPJ) | ||
| NR_047595.2:n.4329T= (CENPJ) |