Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24206684_24206685del , CM000668.2:g.24206684_24206685del | GRCh38 |
| NC_000006.11:g.24206912_24206913del , CM000668.1:g.24206912_24206913del | GRCh37 |
| NC_000006.10:g.24314891_24314892del | NCBI36 |
| NG_012829.1:g.156371_156372del | |
| NG_012829.2:g.181611_181612del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_016356.5:c.923-1580_923-1579del MANE Select | NP_057440.2:n.923-1580_923-1579del |
| ENST00000378454.8:c.923-1580_923-1579del MANE Select | ENSP00000367715.3:n.923-1580_923-1579del |
| NM_001195610.1:c.923-1580_923-1579del | NP_001182539.1:n.923-1580_923-1579del |
| NM_001195610.2:c.923-1580_923-1579del | NP_001182539.1:n.923-1580_923-1579del |
| NM_016356.4:c.923-1580_923-1579del | NP_057440.2:n.923-1580_923-1579del |
| ENST00000378454.7:c.923-1580_923-1579del | ENSP00000367715.3:n.923-1580_923-1579del |