ClinVar Variation:
COSMIC:
dbSNP:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7577013del , CM000668.2:g.7577013del | GRCh38 |
| NC_000006.11:g.7577246del , CM000668.1:g.7577246del | GRCh37 |
| NC_000006.10:g.7522245del | NCBI36 |
| NG_008803.1:g.40377del , LRG_423:g.40377del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.2848del | ENSP00000518230.1:p.Ile950LeufsTer27 | |
| ENST00000379802.8:c.2848del MANE Select | ENSP00000369129.3:p.Ile950LeufsTer27 | |
| ENST00000379802.7:c.2848del | ENSP00000369129.3:p.Ile950LeufsTer27 | |
| ENST00000418664.2:c.2848del | ENSP00000396591.2:p.Ile950LeufsTer27 | |
| NM_001008844.1:c.2848del | NP_001008844.1:p.Ile950LeufsTer27 | |
| NM_004415.2:c.2848del , LRG_423t1:c.2848del | NP_004406.2:p.Ile950LeufsTer27 | |
| XM_011514323.1:c.2848del | XP_011512625.1:p.Ile950LeufsTer27 | |
| NM_001008844.2:c.2848del | NP_001008844.1:p.Ile950LeufsTer27 | |
| NM_001319034.1:c.2848del | NP_001305963.1:p.Ile950LeufsTer27 | |
| NM_004415.3:c.2848del | NP_004406.2:p.Ile950LeufsTer27 | |
| NM_004415.4:c.2848del MANE Select | NP_004406.2:p.Ile950LeufsTer27 | |
| NM_001008844.3:c.2848del | NP_001008844.1:p.Ile950LeufsTer27 | |
| NM_001319034.2:c.2848del | NP_001305963.1:p.Ile950LeufsTer27 |