Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137199287del , CM000671.2:g.137199287del | GRCh38 |
| NC_000009.11:g.140093739del , CM000671.1:g.140093739del | GRCh37 |
| NC_000009.10:g.139213560del | NCBI36 |
| NG_027801.1:g.6427del | |
| NG_027801.2:g.9909del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409012.6:c.1427del MANE Select | ENSP00000387100.4:p.Pro476ArgfsTer? | |
| ENST00000333046.8:c.821del | ENSP00000327617.4:p.Pro274ArgfsTer? | |
| ENST00000409012.4:c.1427del | ENSP00000387100.4:p.Pro476ArgfsTer? | |
| ENST00000541945.1:n.90+4819del | ||
| NM_001128228.2:c.1427del | NP_001121700.2:p.Pro476ArgfsTer? | |
| NM_001128228.3:c.1427del MANE Select | NP_001121700.2:p.Pro476ArgfsTer? |