Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48304028del , CM000675.2:g.48304028del | GRCh38 |
| NC_000013.10:g.48878164del , CM000675.1:g.48878164del | GRCh37 |
| NC_000013.9:g.47776165del | NCBI36 |
| NG_009009.1:g.5282del , LRG_517:g.5282del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.116del MANE Select | ENSP00000267163.4:p.Pro39ArgfsTer26 | |
| ENST00000646097.1:c.116del | ENSP00000496556.1:p.Pro39ArgfsTer26 | |
| ENST00000650461.1:c.116del | ENSP00000497193.1:p.Pro39ArgfsTer26 | |
| ENST00000267163.4:c.116del | ENSP00000267163.4:p.Pro39ArgfsTer26 | |
| ENST00000467505.5:c.116del | ENSP00000434702.1:p.Pro39ArgfsTer? | |
| ENST00000525036.1:n.278del | ||
| NM_000321.2:c.116del , LRG_517t1:c.116del | NP_000312.2:p.Pro39ArgfsTer26 | |
| NM_000321.3:c.116del MANE Select | NP_000312.2:p.Pro39ArgfsTer26 |