Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240877600del , CM000664.2:g.240877600del | GRCh38 |
| NC_000002.11:g.241817017del , CM000664.1:g.241817017del | GRCh37 |
| NC_000002.10:g.241465690del | NCBI36 |
| NG_008005.1:g.13856del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.910del MANE Select | ENSP00000302620.3:p.Ala304HisfsTer8 | |
| ENST00000307503.3:c.910del | ENSP00000302620.3:p.Ala304HisfsTer8 | |
| ENST00000470255.1:n.688del | ||
| NM_000030.2:c.910del | NP_000021.1:p.Ala304HisfsTer8 | |
| NM_000030.3:c.910del MANE Select | NP_000021.1:p.Ala304HisfsTer8 |