Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116832932dup , CM000673.2:g.116832932dup | GRCh38 |
| NC_000011.9:g.116703648dup , CM000673.1:g.116703648dup | GRCh37 |
| NC_000011.8:g.116208858dup | NCBI36 |
| NG_008949.1:g.8025dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227667.8:c.*48dup MANE Select | ENSP00000227667.2:n.*48dup | |
| ENST00000227667.7:c.*48dup | ENSP00000227667.2:n.*48dup | |
| ENST00000375345.3:c.*48dup | ENSP00000364494.1:n.*48dup | |
| ENST00000630701.1:c.402dup | ENSP00000486182.1:n.402dup | |
| NM_000040.1:c.*48dup | NP_000031.1:n.*48dup | |
| NM_000040.2:c.*48dup | NP_000031.1:n.*48dup | |
| NM_000040.3:c.*48dup MANE Select | NP_000031.1:n.*48dup |