Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189001440del , CM000664.2:g.189001440del | GRCh38 |
| NC_000002.11:g.189866166del , CM000664.1:g.189866166del | GRCh37 |
| NC_000002.10:g.189574411del | NCBI36 |
| NG_007404.1:g.32068del , LRG_3:g.32068del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.2228del | ENSP00000415346.2:p.Pro743LeufsTer15 | |
| ENST00000304636.9:c.2327del MANE Select | ENSP00000304408.4:p.Pro776LeufsTer15 | |
| ENST00000304636.7:c.2327del | ENSP00000304408.3:p.Pro776LeufsTer15 | |
| ENST00000317840.9:c.2327del | ENSP00000315243.6:p.Pro776LeufsTer15 | |
| NM_000090.3:c.2327del , LRG_3t1:c.2327del | NP_000081.1:p.Pro776LeufsTer15 | |
| NM_000090.4:c.2327del MANE Select | NP_000081.2:p.Pro776LeufsTer15 |