Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94030591_94030592insA , CM000663.2:g.94030591_94030592insA | GRCh38 |
| NC_000001.10:g.94496147_94496148insA , CM000663.1:g.94496147_94496148insA | GRCh37 |
| NC_000001.9:g.94268735_94268736insA | NCBI36 |
| NG_009073.1:g.95558_95559insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4254-66_4254-65insT MANE Select | ENSP00000359245.3:n.4254-66_4254-65insT | |
| ENST00000370225.3:c.4254-66_4254-65insT | ENSP00000359245.3:n.4254-66_4254-65insT | |
| ENST00000536513.5:c.630-66_630-65insT | ENSP00000439707.2:n.630-66_630-65insT | |
| NM_000350.2:c.4254-66_4254-65insT | NP_000341.2:n.4254-66_4254-65insT | |
| NM_000350.3:c.4254-66_4254-65insT MANE Select | NP_000341.2:n.4254-66_4254-65insT |