Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24800255dup , CM000666.2:g.24800255dup | GRCh38 |
| NC_000004.11:g.24801877dup , CM000666.1:g.24801877dup | GRCh37 |
| NC_000004.10:g.24410975dup | NCBI36 |
| NG_012213.1:g.9793dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.*11dup MANE Select | ENSP00000371554.3:n.*11dup | |
| ENST00000382120.3:c.*11dup | ENSP00000371554.3:n.*11dup | |
| NM_003102.2:c.*11dup | NP_003093.2:n.*11dup | |
| XR_427488.1:n.924dup | ||
| NM_003102.3:c.*11dup | NP_003093.2:n.*11dup | |
| NM_003102.4:c.*11dup MANE Select | NP_003093.2:n.*11dup |