Linked Data
COSMIC:
COSN15544885
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114705568dup , CM000663.2:g.114705568dup | GRCh38 |
| NC_000001.10:g.115248189dup , CM000663.1:g.115248189dup | GRCh37 |
| NC_000001.9:g.115049712dup | NCBI36 |
| NG_007572.1:g.16328dup , LRG_92:g.16328dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.*2527dup MANE Select | ENSP00000358548.4:n.*2527dup | |
| ENST00000369535.4:c.*2527dup | ENSP00000358548.4:n.*2527dup | |
| NM_002524.4:c.*2527dup | NP_002515.1:n.*2527dup | |
| NM_002524.5:c.*2527dup MANE Select | NP_002515.1:n.*2527dup |