Linked Data
COSMIC:
COSM4613182
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.106033611del , CM000685.2:g.106033611del | GRCh38 |
| NC_000023.10:g.105277602del , CM000685.1:g.105277602del | GRCh37 |
| NC_000023.9:g.105164258del | NCBI36 |
| NG_021252.1:g.10119del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372563.2:c.1139del MANE Select | ENSP00000361644.1:p.Phe380SerfsTer15 | |
| ENST00000327674.8:c.1139del | ENSP00000329374.4:p.Phe380SerfsTer15 | |
| ENST00000372563.1:c.1139del | ENSP00000361644.1:p.Phe380SerfsTer15 | |
| NM_000354.5:c.1139del | NP_000345.2:p.Phe380SerfsTer15 | |
| XM_006724683.1:c.1169del | XP_006724746.1:p.Phe390SerfsTer15 | |
| XM_005262180.4:c.*84del | XP_005262237.1:n.*84del | |
| XM_006724683.2:c.1169del | XP_006724746.1:p.Phe390SerfsTer15 | |
| NM_000354.6:c.1139del MANE Select | NP_000345.2:p.Phe380SerfsTer15 |