Linked Data
COSMIC:
COSN19154724
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.185143302dup , CM000666.2:g.185143302dup | GRCh38 |
| NC_000004.11:g.186064456dup , CM000666.1:g.186064456dup | GRCh37 |
| NC_000004.10:g.186301450dup | NCBI36 |
| NG_013001.1:g.5040dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000281456.11:c.-71dup MANE Select | ENSP00000281456.5:n.-71dup | |
| ENST00000281456.10:c.-71dup | ENSP00000281456.5:n.-71dup | |
| ENST00000491736.1:c.-71dup | ENSP00000476711.1:n.-71dup | |
| NM_001151.3:c.-71dup | NP_001142.2:n.-71dup | |
| NM_001151.4:c.-71dup MANE Select | NP_001142.2:n.-71dup |