Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55091504_55091506del , CM000666.2:g.55091504_55091506del | GRCh38 |
| NC_000004.11:g.55957671_55957673del , CM000666.1:g.55957671_55957673del | GRCh37 |
| NC_000004.10:g.55652428_55652430del | NCBI36 |
| NG_012004.1:g.39096_39098del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.3069+1117_3069+1119del MANE Select | ENSP00000263923.4:n.3069+1117_3069+1119del | |
| ENST00000647068.1:n.3082+1117_3082+1119del | ||
| ENST00000263923.4:c.3069+1117_3069+1119del | ENSP00000263923.4:n.3069+1117_3069+1119del | |
| NM_002253.2:c.3069+1117_3069+1119del | NP_002244.1:n.3069+1117_3069+1119del | |
| NM_002253.3:c.3069+1117_3069+1119del | NP_002244.1:n.3069+1117_3069+1119del | |
| NM_002253.4:c.3069+1117_3069+1119del MANE Select | NP_002244.1:n.3069+1117_3069+1119del |