Linked Data
COSMIC:
COSN17076196
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114705456_114705457insT , CM000663.2:g.114705456_114705457insT | GRCh38 |
| NC_000001.10:g.115248077_115248078insT , CM000663.1:g.115248077_115248078insT | GRCh37 |
| NC_000001.9:g.115049600_115049601insT | NCBI36 |
| NG_007572.1:g.16438_16439insA , LRG_92:g.16438_16439insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.*2637_*2638insA MANE Select | ENSP00000358548.4:n.*2637_*2638insA | |
| ENST00000369535.4:c.*2637_*2638insA | ENSP00000358548.4:n.*2637_*2638insA | |
| NM_002524.4:c.*2637_*2638insA | NP_002515.1:n.*2637_*2638insA | |
| NM_002524.5:c.*2637_*2638insA MANE Select | NP_002515.1:n.*2637_*2638insA |