Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114709456_114709458delinsAAT , CM000663.2:g.114709456_114709458delinsAAT | GRCh38 |
| NC_000001.10:g.115252077_115252079delinsAAT , CM000663.1:g.115252077_115252079delinsAAT | GRCh37 |
| NC_000001.9:g.115053600_115053602delinsAAT | NCBI36 |
| NG_007572.1:g.12437_12439delinsATT , LRG_92:g.12437_12439delinsATT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.450+111_450+113delinsATT MANE Select | ENSP00000358548.4:n.450+111_450+113delinsATT | |
| ENST00000369535.4:c.450+111_450+113delinsATT | ENSP00000358548.4:n.450+111_450+113delinsATT | |
| NM_002524.4:c.450+111_450+113delinsATT | NP_002515.1:n.450+111_450+113delinsATT | |
| NM_002524.5:c.450+111_450+113delinsATT MANE Select | NP_002515.1:n.450+111_450+113delinsATT |