Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.86513395_86513396insT , CM000678.2:g.86513395_86513396insT | GRCh38 |
| NC_000016.9:g.86547001_86547002insT , CM000678.1:g.86547001_86547002insT | GRCh37 |
| NC_000016.8:g.85104502_85104503insT | NCBI36 |
| NG_016273.1:g.7869_7870insT |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001451.3:c.*310_*311insT MANE Select | NP_001442.2:n.*310_*311insT |
| ENST00000262426.6:c.*310_*311insT MANE Select | ENSP00000262426.4:n.*310_*311insT |
| NM_001451.2:c.*310_*311insT | NP_001442.2:n.*310_*311insT |
| ENST00000262426.5:c.*310_*311insT | ENSP00000262426.4:n.*310_*311insT |