Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5225652_5225655delinsGGCA , CM000673.2:g.5225652_5225655delinsGGCA | GRCh38 |
| NC_000011.9:g.5246882_5246885delinsGGCA , CM000673.1:g.5246882_5246885delinsGGCA | GRCh37 |
| NC_000011.8:g.5203458_5203461delinsGGCA | NCBI36 |
| NG_000007.3:g.71961_71964delinsTGCC | |
| NG_059281.1:g.6417_6420delinsTGCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.387_390delinsTGCC | ENSP00000494175.1:p.Ala129= | |
| ENST00000335295.4:c.387_390delinsTGCC MANE Select | ENSP00000333994.3:p.Ala129= | |
| ENST00000633227.1:c.*203_*206delinsTGCC | ENSP00000488004.1:n.*203_*206delinsTGCC | |
| NM_000518.4:c.387_390delinsTGCC | NP_000509.1:p.Ala129= | |
| NM_000518.5:c.387_390delinsTGCC MANE Select | NP_000509.1:p.Ala129= |