Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129530506_129530551delinsAACACACACACACACACACACACACACAACACACACACACACACAC , CM000665.2:g.129530506_129530551delinsAACACACACACACACACACACACACACAACACACACACACACACAC | GRCh38 |
| NC_000003.11:g.129249349_129249394delinsAACACACACACACACACACACACACACAACACACACACACACACAC , CM000665.1:g.129249349_129249394delinsAACACACACACACACACACACACACACAACACACACACACACACAC | GRCh37 |
| NC_000003.10:g.130732039_130732084delinsAACACACACACACACACACACACACACAACACACACACACACACAC | NCBI36 |
| NG_009115.1:g.6868_6913delinsAACACACACACACACACACACACACACAACACACACACACACACAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.362-370_362-325delinsAACACACACACACACACACACACACACAACACACACACACACACAC MANE Select | ENSP00000296271.3:n.362-370_362-325delinsAACACACACACACACACACA... | |
| ENST00000296271.3:c.362-370_362-325delinsAACACACACACACACACACACACACACAACACACACACACACACAC | ENSP00000296271.3:n.362-370_362-325delinsAACACACACACACACACACA... | |
| NM_000539.3:c.362-370_362-325delinsAACACACACACACACACACACACACACAACACACACACACACACAC MANE Select | NP_000530.1:n.362-370_362-325delinsAACACACACACACACACACACACACA... |