Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.73683402A= , CM000669.2:g.73683402A= | GRCh38 |
| NC_000007.13:g.73097732A= , CM000669.1:g.73097732A= | GRCh37 |
| NC_000007.12:g.72735668A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395176.3:c.22T= (DNAJC30) MANE Select | ENSP00000378605.1:p.Trp8= | |
| ENST00000395176.2:c.22T= (DNAJC30) | ENSP00000378605.1:p.Trp8= | |
| ENST00000464615.1:n.359+19A= (BUD23) | ||
| NM_032317.2:c.22T= (DNAJC30) | NP_115693.2:p.Trp8= | |
| NM_032317.3:c.22T= (DNAJC30) MANE Select | NP_115693.2:p.Trp8= |