Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19961712_19961713del , CM000670.2:g.19961712_19961713del | GRCh38 |
| NC_000008.10:g.19819223_19819224del , CM000670.1:g.19819223_19819224del | GRCh37 |
| NC_000008.9:g.19863503_19863504del | NCBI36 |
| NG_008855.1:g.27642_27643del | |
| NG_008855.2:g.64996_64997del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.1323-403_1323-402del MANE Select | ENSP00000497642.1:n.1323-403_1323-402del | |
| ENST00000650478.1:c.263-403_263-402del | ENSP00000497560.1:n.263-403_263-402del | |
| ENST00000311322.8:c.1323-403_1323-402del | ENSP00000309757.6:n.1323-403_1323-402del | |
| NM_000237.2:c.1323-403_1323-402del | NP_000228.1:n.1323-403_1323-402del | |
| NM_000237.3:c.1323-403_1323-402del MANE Select | NP_000228.1:n.1323-403_1323-402del |