Linked Data
COSMIC:
COSN22173391
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114706754_114706755insT , CM000663.2:g.114706754_114706755insT | GRCh38 |
| NC_000001.10:g.115249375_115249376insT , CM000663.1:g.115249375_115249376insT | GRCh37 |
| NC_000001.9:g.115050898_115050899insT | NCBI36 |
| NG_007572.1:g.15140_15141insA , LRG_92:g.15140_15141insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.*1339_*1340insA MANE Select | ENSP00000358548.4:n.*1339_*1340insA | |
| ENST00000369535.4:c.*1339_*1340insA | ENSP00000358548.4:n.*1339_*1340insA | |
| NM_002524.4:c.*1339_*1340insA | NP_002515.1:n.*1339_*1340insA | |
| NM_002524.5:c.*1339_*1340insA MANE Select | NP_002515.1:n.*1339_*1340insA |