Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.83509032_83509034delinsAGG , CM000685.2:g.83509032_83509034delinsAGG | GRCh38 |
| NG_009936.2:g.5772_5774delinsAGG |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000307.5:c.708_710delinsAGG MANE Select | NP_000298.3:p.Ala237Gly |
| ENST00000644024.2:c.708_710delinsAGG MANE Select | ENSP00000495996.1:p.Ala237Gly |
| NM_000307.4:c.708_710delinsAGG | NP_000298.3:p.Ala237Gly |
| ENST00000373200.4:c.708_710delinsAGG | ENSP00000362296.2:p.Ala237Gly |