Linked Data
COSMIC:
COSN24304762
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48045804_48045805insT , CM000675.2:g.48045804_48045805insT | GRCh38 |
| NC_000013.10:g.48619940_48619941insT , CM000675.1:g.48619940_48619941insT | GRCh37 |
| NC_000013.9:g.47517941_47517942insT | NCBI36 |
| NG_047021.1:g.13238_13239insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258662.3:c.*5_*6insT MANE Select | ENSP00000258662.1:n.*5_*6insT | |
| ENST00000258662.2:c.*5_*6insT | ENSP00000258662.1:n.*5_*6insT | |
| NM_018283.2:c.*5_*6insT | NP_060753.1:n.*5_*6insT | |
| NM_018283.3:c.*5_*6insT | NP_060753.1:n.*5_*6insT | |
| NR_136687.1:n.680_681insT | ||
| NR_136688.1:n.675+5_675+6insT | ||
| NM_018283.4:c.*5_*6insT MANE Select | NP_060753.1:n.*5_*6insT | |
| NR_136687.2:n.521_522insT | ||
| NR_136688.2:n.516+5_516+6insT |