Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68231629dup , CM000672.2:g.68231629dup | GRCh38 |
| NC_000010.10:g.69991386dup , CM000672.1:g.69991386dup | GRCh37 |
| NC_000010.9:g.69661392dup | NCBI36 |
| NG_031934.1:g.5489dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373673.5:c.53dup MANE Select | ENSP00000362777.3:p.Cys19ValfsTer? | |
| ENST00000373673.4:c.53dup | ENSP00000362777.3:p.Cys19ValfsTer? | |
| NM_145178.3:c.53dup | NP_660161.1:p.Cys19ValfsTer? | |
| NM_145178.4:c.53dup MANE Select | NP_660161.1:p.Cys19ValfsTer? |