Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109264392_109264393insAA , CM000663.2:g.109264392_109264393insAA | GRCh38 |
| NC_000001.10:g.109807014_109807015insAA , CM000663.1:g.109807014_109807015insAA | GRCh37 |
| NC_000001.9:g.109608537_109608538insAA | NCBI36 |
| NG_052669.1:g.19688_19689insAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271332.4:c.5289+27_5289+28insAA MANE Select | ENSP00000271332.3:n.5289+27_5289+28insAA | |
| ENST00000271332.3:c.5289+27_5289+28insAA | ENSP00000271332.3:n.5289+27_5289+28insAA | |
| NM_001408.2:c.5289+27_5289+28insAA | NP_001399.1:n.5289+27_5289+28insAA | |
| XM_005270580.3:c.5289+27_5289+28insAA | XP_005270637.1:n.5289+27_5289+28insAA | |
| NM_001408.3:c.5289+27_5289+28insAA MANE Select | NP_001399.1:n.5289+27_5289+28insAA |