Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583523_41583524insAGCG , CM000679.2:g.41583523_41583524insAGCG | GRCh38 |
| NC_000017.10:g.39739775_39739776insAGCG , CM000679.1:g.39739775_39739776insAGCG | GRCh37 |
| NC_000017.9:g.36993301_36993302insAGCG | NCBI36 |
| NG_008624.1:g.8373_8374insGCTC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.1053+28_1053+29insGCTC MANE Select | ENSP00000167586.6:n.1053+28_1053+29insGCTC | |
| ENST00000167586.6:c.1053+28_1053+29insGCTC | ENSP00000167586.6:n.1053+28_1053+29insGCTC | |
| ENST00000476662.1:n.503+28_503+29insGCTC | ||
| NM_000526.4:c.1053+28_1053+29insGCTC | NP_000517.2:n.1053+28_1053+29insGCTC | |
| NM_000526.5:c.1053+28_1053+29insGCTC MANE Select | NP_000517.3:n.1053+28_1053+29insGCTC |