Linked Data
dbSNP Id:
rs1944081287
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128891431_128891454del , CM000673.2:g.128891431_128891454del | GRCh38 |
| NC_000011.9:g.128761326_128761349del , CM000673.1:g.128761326_128761349del | GRCh37 |
| NC_000011.8:g.128266536_128266559del | NCBI36 |
| NG_023406.2:g.5014_5037del , LRG_333:g.5014_5037del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529694.6:c.-301_-278del MANE Select | ENSP00000433295.1:n.-301_-278del | |
| ENST00000529694.5:c.-301_-278del | ENSP00000433295.1:n.-301_-278del | |
| NM_000890.3:c.-301_-278del , LRG_333t1:c.-301_-278del | NP_000881.3:n.-301_-278del | |
| NM_000890.4:c.-301_-278del | NP_000881.3:n.-301_-278del | |
| NM_001354169.1:c.-390_-367del | NP_001341098.1:n.-390_-367del | |
| NM_000890.5:c.-301_-278del MANE Select | NP_000881.3:n.-301_-278del | |
| NM_001354169.2:c.-390_-367del | NP_001341098.1:n.-390_-367del |