Linked Data
COSMIC:
COSN16128601
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31659703_31659704insG , CM000683.2:g.31659703_31659704insG | GRCh38 |
| NC_000021.8:g.33032016_33032017insG , CM000683.1:g.33032016_33032017insG | GRCh37 |
| NC_000021.7:g.31953887_31953888insG | NCBI36 |
| NG_008689.1:g.5082_5083insG , LRG_652:g.5082_5083insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.-67_-66insG MANE Select | ENSP00000270142.7:n.-67_-66insG | |
| ENST00000270142.10:c.-67_-66insG | ENSP00000270142.6:n.-67_-66insG | |
| ENST00000389995.4:c.-67_-66insG | ENSP00000374645.4:n.-67_-66insG | |
| ENST00000476106.5:n.11_12insG | ||
| NM_000454.4:c.-67_-66insG , LRG_652t1:c.-67_-66insG | NP_000445.1:n.-67_-66insG | |
| NM_000454.5:c.-67_-66insG MANE Select | NP_000445.1:n.-67_-66insG |