Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.155290224_155290226delinsCCT , CM000663.2:g.155290224_155290226delinsCCT | GRCh38 |
| NC_000001.10:g.155260015_155260017delinsCCT , CM000663.1:g.155260015_155260017delinsCCT | GRCh37 |
| NC_000001.9:g.153526639_153526641delinsCCT | NCBI36 |
| NG_011677.1:g.16209_16211delinsAGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342741.6:c.*346_*348delinsAGG MANE Select | ENSP00000339933.4:n.*346_*348delinsAGG | |
| ENST00000392414.7:c.*346_*348delinsAGG | ENSP00000376214.3:n.*346_*348delinsAGG | |
| NM_000298.5:c.*346_*348delinsAGG | NP_000289.1:n.*346_*348delinsAGG | |
| NM_181871.3:c.*346_*348delinsAGG | NP_870986.1:n.*346_*348delinsAGG | |
| NM_000298.6:c.*346_*348delinsAGG MANE Select | NP_000289.1:n.*346_*348delinsAGG | |
| NM_181871.4:c.*346_*348delinsAGG | NP_870986.1:n.*346_*348delinsAGG |