Linked Data
COSMIC:
COSN18729891
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177992664_177992665insT , CM000667.2:g.177992664_177992665insT | GRCh38 |
| NC_000005.9:g.177419665_177419666insT , CM000667.1:g.177419665_177419666insT | GRCh37 |
| NC_000005.8:g.177352271_177352272insT | NCBI36 |
| NG_015889.1:g.8578_8579insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308304.2:c.*44_*45insA MANE Select | ENSP00000311290.2:n.*44_*45insA | |
| NM_006261.4:c.*44_*45insA | NP_006252.3:n.*44_*45insA | |
| NM_006261.5:c.*44_*45insA MANE Select | NP_006252.4:n.*44_*45insA |