Linked Data
COSMIC:
COSN21092855
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94989067_94989068insT , CM000672.2:g.94989067_94989068insT | GRCh38 |
| NC_000010.10:g.96748824_96748825insT , CM000672.1:g.96748824_96748825insT | GRCh37 |
| NC_000010.9:g.96738814_96738815insT | NCBI36 |
| NG_008385.1:g.55410_55411insT | |
| NG_008385.2:g.55910_55911insT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.*39_*40insT MANE Select | ENSP00000260682.6:n.*39_*40insT | |
| ENST00000643112.1:c.*521_*522insT | ENSP00000496202.1:n.*521_*522insT | |
| ENST00000260682.6:c.*39_*40insT | ENSP00000260682.6:n.*39_*40insT | |
| NM_000771.3:c.*39_*40insT | NP_000762.2:n.*39_*40insT | |
| NM_000771.4:c.*39_*40insT MANE Select | NP_000762.2:n.*39_*40insT |