Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133538906_133538907delinsAT , CM000672.2:g.133538906_133538907delinsAT | GRCh38 |
| NC_000010.10:g.135352410_135352411delinsAT , CM000672.1:g.135352410_135352411delinsAT | GRCh37 |
| NC_000010.9:g.135202400_135202401delinsAT | NCBI36 |
| NG_008383.1:g.16544_16545delinsAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252945.8:c.1424_1425delinsAT MANE Select | ENSP00000252945.3:p.His475= | |
| ENST00000252945.7:c.1424_1425delinsAT | ENSP00000252945.3:p.His475= | |
| ENST00000368520.1:n.1358+1014_1358+1015delinsAT | ||
| ENST00000463117.6:c.1424_1425delinsAT | ENSP00000440689.1:p.His475= | |
| ENST00000469258.1:n.520_521delinsAT | ||
| NM_000773.3:c.1424_1425delinsAT | NP_000764.1:p.His475= | |
| NM_000773.4:c.1424_1425delinsAT MANE Select | NP_000764.1:p.His475= |