Linked Data
COSMIC:
COSN231008
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94418474del , CM000663.2:g.94418474del | GRCh38 |
| NC_000001.10:g.94884030del , CM000663.1:g.94884030del | GRCh37 |
| NC_000001.9:g.94656618del | NCBI36 |
| NG_008865.1:g.5098del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370214.9:c.-5del MANE Select | ENSP00000359233.4:n.-5del | |
| ENST00000647998.2:c.-5del | ENSP00000497921.2:n.-5del | |
| ENST00000370214.8:c.-5del | ENSP00000359233.4:n.-5del | |
| NM_001122674.1:c.-5del | NP_001116146.1:n.-5del | |
| NM_002858.3:c.-5del | NP_002849.1:n.-5del | |
| XM_006710802.2:c.-5del | XP_006710865.2:n.-5del | |
| NM_002858.4:c.-5del MANE Select | NP_002849.1:n.-5del | |
| NM_001122674.2:c.-5del | NP_001116146.1:n.-5del |