Linked Data
COSMIC:
COSN21450540
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159316068_159316069insG , CM000667.2:g.159316068_159316069insG | GRCh38 |
| NC_000005.9:g.158743076_158743077insG , CM000667.1:g.158743076_158743077insG | GRCh37 |
| NC_000005.8:g.158675654_158675655insG | NCBI36 |
| NG_009618.1:g.19405_19406insC , LRG_71:g.19405_19406insC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696750.1:c.*32_*33insC | ENSP00000512849.1:n.*32_*33insC | |
| ENST00000696751.1:c.*514_*515insC | ENSP00000512850.1:n.*514_*515insC | |
| ENST00000231228.3:c.*32_*33insC MANE Select | ENSP00000231228.2:n.*32_*33insC | |
| ENST00000231228.2:c.*32_*33insC | ENSP00000231228.2:n.*32_*33insC | |
| NM_002187.2:c.*32_*33insC , LRG_71t1:c.*32_*33insC | NP_002178.2:n.*32_*33insC | |
| NM_002187.3:c.*32_*33insC MANE Select | NP_002178.2:n.*32_*33insC |