Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74259845_74259847delinsAGG , CM000676.2:g.74259845_74259847delinsAGG | GRCh38 |
| NC_000014.8:g.74726548_74726550delinsAGG , CM000676.1:g.74726548_74726550delinsAGG | GRCh37 |
| NC_000014.7:g.73796301_73796303delinsAGG | NCBI36 |
| NG_013092.1:g.25374_25376delinsAGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261980.3:c.760+63_760+65delinsAGG MANE Select | ENSP00000261980.2:n.760+63_760+65delinsAGG | |
| ENST00000261980.2:c.760+63_760+65delinsAGG | ENSP00000261980.2:n.760+63_760+65delinsAGG | |
| NM_182894.2:c.760+63_760+65delinsAGG | NP_878314.1:n.760+63_760+65delinsAGG | |
| XM_011536719.1:c.760+63_760+65delinsAGG | XP_011535021.1:n.760+63_760+65delinsAGG | |
| NM_182894.3:c.760+63_760+65delinsAGG MANE Select | NP_878314.1:n.760+63_760+65delinsAGG |