Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39666007del , CM000679.2:g.39666007del | GRCh38 |
| NC_000017.10:g.37822260del , CM000679.1:g.37822260del | GRCh37 |
| NC_000017.9:g.35075786del | NCBI36 |
| NG_008892.1:g.5662del , LRG_210:g.5662del | |
| NG_042278.1:g.3027del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.402del MANE Select | ENSP00000312624.2:p.Glu135ArgfsTer? | |
| ENST00000309889.2:c.402del | ENSP00000312624.2:p.Glu135ArgfsTer? | |
| ENST00000578283.1:c.330del | ENSP00000462787.1:p.Glu111ArgfsTer? | |
| NM_003673.3:c.402del , LRG_210t1:c.402del | NP_003664.1:p.Glu135ArgfsTer? | |
| NM_003673.4:c.402del MANE Select | NP_003664.1:p.Glu135ArgfsTer? |