Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48045606_48045607insT , CM000675.2:g.48045606_48045607insT | GRCh38 |
| NC_000013.10:g.48619742_48619743insT , CM000675.1:g.48619742_48619743insT | GRCh37 |
| NC_000013.9:g.47517743_47517744insT | NCBI36 |
| NG_047021.1:g.13040_13041insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258662.3:c.356-54_356-53insT MANE Select | ENSP00000258662.1:n.356-54_356-53insT | |
| ENST00000258662.2:c.356-54_356-53insT | ENSP00000258662.1:n.356-54_356-53insT | |
| NM_018283.2:c.356-54_356-53insT | NP_060753.1:n.356-54_356-53insT | |
| NM_018283.3:c.356-54_356-53insT | NP_060753.1:n.356-54_356-53insT | |
| NR_136687.1:n.536-54_536-53insT | ||
| NR_136688.1:n.536-54_536-53insT | ||
| NM_018283.4:c.356-54_356-53insT MANE Select | NP_060753.1:n.356-54_356-53insT | |
| NR_136687.2:n.377-54_377-53insT | ||
| NR_136688.2:n.377-54_377-53insT |