Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869302_240869304del , CM000664.2:g.240869302_240869304del | GRCh38 |
| NC_000002.11:g.241808719_241808721del , CM000664.1:g.241808719_241808721del | GRCh37 |
| NC_000002.10:g.241457392_241457394del | NCBI36 |
| NG_008005.1:g.5558_5560del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.298_300del MANE Select | ENSP00000302620.3:p.Phe100del | |
| ENST00000307503.3:c.298_300del | ENSP00000302620.3:p.Phe100del | |
| ENST00000472436.1:n.318_320del | ||
| NM_000030.2:c.298_300del | NP_000021.1:p.Phe100del | |
| XR_924060.1:n.405+930_405+932del | ||
| NM_000030.3:c.298_300del MANE Select | NP_000021.1:p.Phe100del |