Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28768677_28768681delinsACTGT , CM000676.2:g.28768677_28768681delinsACTGT | GRCh38 |
| NC_000014.8:g.29237883_29237887delinsACTGT , CM000676.1:g.29237883_29237887delinsACTGT | GRCh37 |
| NC_000014.7:g.28307634_28307638delinsACTGT | NCBI36 |
| NG_009367.1:g.6597_6601delinsACTGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706482.1:c.1398_1402delinsACTGT | ENSP00000516406.1:p.Gly466= | |
| ENST00000313071.7:c.1398_1402delinsACTGT MANE Select | ENSP00000339004.3:p.Gly466= | |
| ENST00000313071.6:c.1398_1402delinsACTGT | ENSP00000339004.3:p.Gly466= | |
| NM_005249.4:c.1398_1402delinsACTGT | NP_005240.3:p.Gly466= | |
| NM_005249.5:c.1398_1402delinsACTGT MANE Select | NP_005240.3:p.Gly466= |