Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115390_10115391del , CM000681.2:g.10115390_10115391del | GRCh38 |
| NC_000019.9:g.10226066_10226067del , CM000681.1:g.10226066_10226067del | GRCh37 |
| NC_000019.8:g.10087066_10087067del | NCBI36 |
| NG_047007.1:g.8870_8871del | |
| NG_051197.1:g.9534_9535del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.947+88_947+89del MANE Select | ENSP00000253108.3:n.947+88_947+89del | |
| ENST00000253108.8:c.947+88_947+89del | ENSP00000253108.3:n.947+88_947+89del | |
| ENST00000590158.1:n.966+88_966+89del | ||
| ENST00000593054.5:c.341+88_341+89del | ENSP00000467187.1:n.341+88_341+89del | |
| NM_003755.3:c.947+88_947+89del | NP_003746.2:n.947+88_947+89del | |
| NM_003755.4:c.947+88_947+89del | NP_003746.2:n.947+88_947+89del | |
| NM_003755.5:c.947+88_947+89del MANE Select | NP_003746.2:n.947+88_947+89del |