Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67611979del , CM000673.2:g.67611979del | GRCh38 |
| NC_000011.9:g.67379450del , CM000673.1:g.67379450del | GRCh37 |
| NC_000011.8:g.67136026del | NCBI36 |
| NG_013353.1:g.10128del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322776.11:c.1162+1del | ||
| ENST00000647561.1:c.1162+1del | ||
| ENST00000322776.10:c.1162+1del | ||
| ENST00000415352.6:c.1141+1del | ||
| ENST00000526770.5:n.1445+1del | ||
| ENST00000527355.5:c.370-141del | ENSP00000432637.1:n.370-141del | |
| ENST00000527923.1:n.504+1del | ||
| ENST00000529927.5:c.1135+1del | ||
| ENST00000531250.1:n.426+1del | ||
| ENST00000532303.5:c.859+1del | ||
| ENST00000533919.5:c.566+1del | ||
| ENST00000534352.1:n.261del | ||
| NM_001166102.1:c.1135+1del | ||
| NM_007103.3:c.1162+1del | ||
| NM_001166102.2:c.1135+1del | ||
| NM_007103.4:c.1162+1del |