Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1213344_1213348del , CM000667.2:g.1213344_1213348del | GRCh38 |
| NC_000005.9:g.1213459_1213463del , CM000667.1:g.1213459_1213463del | GRCh37 |
| NC_000005.8:g.1266459_1266463del | NCBI36 |
| NG_008282.1:g.16750_16754del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304460.11:c.664-119_664-115del MANE Select | ENSP00000305302.10:n.664-119_664-115del | |
| ENST00000304460.10:c.664-119_664-115del | ENSP00000305302.10:n.664-119_664-115del | |
| ENST00000515652.5:c.572-119_572-115del | ENSP00000425701.1:n.572-119_572-115del | |
| NM_001003841.2:c.664-119_664-115del | NP_001003841.1:n.664-119_664-115del | |
| NM_001003841.3:c.664-119_664-115del MANE Select | NP_001003841.1:n.664-119_664-115del |