Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215640720_215640724del , CM000663.2:g.215640720_215640724del | GRCh38 |
| NC_000001.10:g.215814062_215814066del , CM000663.1:g.215814062_215814066del | GRCh37 |
| NC_000001.9:g.213880685_213880689del | NCBI36 |
| NG_009497.1:g.787675_787679del | |
| NG_009497.2:g.787727_787731del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.14804_14808del MANE Select | ENSP00000305941.3:p.Arg4935ProfsTer17 | |
| ENST00000674083.1:c.14804_14808del | ENSP00000501296.1:p.Arg4935ProfsTer17 | |
| ENST00000307340.7:c.14804_14808del | ENSP00000305941.3:p.Arg4935ProfsTer17 | |
| NM_206933.2:c.14804_14808del | NP_996816.2:p.Arg4935ProfsTer17 | |
| NM_206933.3:c.14804_14808del | NP_996816.2:p.Arg4935ProfsTer17 | |
| NM_206933.4:c.14804_14808del MANE Select | NP_996816.3:p.Arg4935ProfsTer17 |