Linked Data
COSMIC:
COSN21597651
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33300457dup , CM000681.2:g.33300457dup | GRCh38 |
| NC_000019.9:g.33791363dup , CM000681.1:g.33791363dup | GRCh37 |
| NC_000019.8:g.38483203dup | NCBI36 |
| NG_012022.1:g.7068dup , LRG_456:g.7068dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000498907.3:c.*881dup MANE Select | ENSP00000427514.1:n.*881dup | |
| ENST00000498907.2:c.*881dup | ENSP00000427514.1:n.*881dup | |
| NM_001285829.1:c.*881dup | NP_001272758.1:n.*881dup | |
| NM_001287424.1:c.*881dup | NP_001274353.1:n.*881dup | |
| NM_001287435.1:c.*881dup | NP_001274364.1:n.*881dup | |
| NM_004364.4:c.*881dup | NP_004355.2:n.*881dup | |
| NM_001287424.2:c.*881dup | NP_001274353.1:n.*881dup | |
| NM_004364.5:c.*881dup MANE Select | NP_004355.2:n.*881dup | |
| NM_001285829.2:c.*881dup | NP_001272758.1:n.*881dup | |
| NM_001287435.2:c.*881dup | NP_001274364.1:n.*881dup |