Linked Data
dbSNP Id:
rs72525532
MyVariant Identifiers:
chr11:g.116660558_116660559insTC (hg19)
chr11:g.116789842_116789843insTC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116789842_116789843insTC , CM000673.2:g.116789842_116789843insTC | GRCh38 |
| NC_000011.9:g.116660558_116660559insTC , CM000673.1:g.116660558_116660559insTC | GRCh37 |
| NC_000011.8:g.116165768_116165769insTC | NCBI36 |
| NG_015894.1:g.7578_7579insGA | |
| NG_015894.2:g.7578_7579insGA |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000227665.9:c.*285_*286insGA MANE Select | ENSP00000227665.4:n.*285_*286insGA | |
| ENST00000227665.8:c.*285_*286insGA | ENSP00000227665.4:n.*285_*286insGA | |
| ENST00000542499.5:c.*285_*286insGA | ENSP00000445002.1:n.*285_*286insGA | |
| NM_001166598.1:c.*285_*286insGA | NP_001160070.1:n.*285_*286insGA | |
| NM_052968.4:c.*285_*286insGA | NP_443200.2:n.*285_*286insGA | |
| NM_001166598.2:c.*285_*286insGA | NP_001160070.1:n.*285_*286insGA | |
| NM_001371904.1:c.*285_*286insGA MANE Select | NP_001358833.1:n.*285_*286insGA | |
| NM_052968.5:c.*285_*286insGA | NP_443200.2:n.*285_*286insGA |