Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99949764_99949774del , CM000666.2:g.99949764_99949774del | GRCh38 |
| NC_000004.11:g.100870921_100870931del , CM000666.1:g.100870921_100870931del | GRCh37 |
| NC_000004.10:g.101089944_101089954del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296417.6:c.4-32_4-22del MANE Select | ENSP00000296417.5:n.4-32_4-22del | |
| ENST00000651623.1:c.4-32_4-22del | ENSP00000498935.1:n.4-32_4-22del | |
| ENST00000296417.5:c.4-32_4-22del | ENSP00000296417.5:n.4-32_4-22del | |
| ENST00000511203.1:n.528_538del | ||
| ENST00000511319.5:n.497_507del | ||
| ENST00000511348.1:n.189-32_189-22del | ||
| ENST00000527366.1:n.88-32_88-22del | ||
| ENST00000529158.5:n.53-32_53-22del | ||
| NM_002106.3:c.4-32_4-22del | NP_002097.1:n.4-32_4-22del | |
| NM_002106.4:c.4-32_4-22del MANE Select | NP_002097.1:n.4-32_4-22del |