Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.64193026del , CM000685.2:g.64193026del | GRCh38 |
| NC_000023.10:g.63412906del , CM000685.1:g.63412906del | GRCh37 |
| NC_000023.9:g.63329631del | NCBI36 |
| NG_021345.1:g.17719del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374869.8:c.261del MANE Select | ENSP00000364003.4:p.Gly89ValfsTer11 | |
| ENST00000330258.3:c.261del | ENSP00000329117.3:p.Gly89ValfsTer11 | |
| ENST00000374869.7:c.261del | ENSP00000364003.3:p.Gly89ValfsTer11 | |
| NM_152424.3:c.261del | NP_689637.3:p.Gly89ValfsTer11 | |
| XM_011530858.1:c.261del | XP_011529160.1:p.Gly89ValfsTer11 | |
| NM_152424.4:c.261del MANE Select | NP_689637.3:p.Gly89ValfsTer11 |