Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154902045del , CM000685.2:g.154902045del | GRCh38 |
| NC_000023.10:g.154130320del , CM000685.1:g.154130320del | GRCh37 |
| NC_000023.9:g.153783514del | NCBI36 |
| NG_011403.1:g.125679del | |
| NG_011403.2:g.125679del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.6115+6del MANE Select | NP_000123.1:n.6115+6del |
| ENST00000360256.9:c.6115+6del MANE Select | ENSP00000353393.4:n.6115+6del |
| NM_000132.3:c.6115+6del | NP_000123.1:n.6115+6del |
| ENST00000360256.8:c.6115+6del | ENSP00000353393.4:n.6115+6del |
| XM_011531126.1:c.6010+6del | XP_011529428.1:n.6010+6del |