Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215728095_215728201del , CM000663.2:g.215728095_215728201del | GRCh38 |
| NC_000001.10:g.215901437_215901543del , CM000663.1:g.215901437_215901543del | GRCh37 |
| NC_000001.9:g.213968060_213968166del | NCBI36 |
| NG_009497.1:g.700198_700304del | |
| NG_009497.2:g.700250_700356del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.11897_12003del MANE Select | ENSP00000305941.3:p.Gln3966LeufsTer11 | |
| ENST00000674083.1:c.11897_12003del | ENSP00000501296.1:p.Gln3966LeufsTer11 | |
| ENST00000307340.7:c.11897_12003del | ENSP00000305941.3:p.Gln3966LeufsTer11 | |
| NM_206933.2:c.11897_12003del | NP_996816.2:p.Gln3966LeufsTer11 | |
| NM_206933.3:c.11897_12003del | NP_996816.2:p.Gln3966LeufsTer11 | |
| NM_206933.4:c.11897_12003del MANE Select | NP_996816.3:p.Gln3966LeufsTer11 |