Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.53051664_53051668delinsTCTAA , CM000675.2:g.53051664_53051668delinsTCTAA | GRCh38 |
| NC_000013.10:g.53625799_53625803delinsTCTAA , CM000675.1:g.53625799_53625803delinsTCTAA | GRCh37 |
| NC_000013.9:g.52523800_52523804delinsTCTAA | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000219022.3:c.*893_*897delinsTCTAA MANE Select | ENSP00000219022.2:n.*893_*897delinsTCTAA | |
| ENST00000219022.2:c.*893_*897delinsTCTAA | ENSP00000219022.2:n.*893_*897delinsTCTAA | |
| NM_006418.4:c.*893_*897delinsTCTAA | NP_006409.3:n.*893_*897delinsTCTAA | |
| NM_006418.5:c.*893_*897delinsTCTAA MANE Select | NP_006409.3:n.*893_*897delinsTCTAA |