Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153736241_153736246del , CM000685.2:g.153736241_153736246del | GRCh38 |
| NC_000023.10:g.153001695_153001700del , CM000685.1:g.153001695_153001700del | GRCh37 |
| NC_000023.9:g.152654889_152654894del | NCBI36 |
| NG_009022.2:g.16374_16379del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1211_1216del MANE Select | ENSP00000218104.3:p.Ser404_Ser405del | |
| ENST00000218104.5:c.1211_1216del | ENSP00000218104.3:p.Ser404_Ser405del | |
| ENST00000443684.2:n.214_219del | ||
| NM_000033.3:c.1211_1216del | NP_000024.2:p.Ser404_Ser405del | |
| XR_938507.1:n.1627_1632del | ||
| XR_938507.2:n.1627_1632del | ||
| NM_000033.4:c.1211_1216del MANE Select | NP_000024.2:p.Ser404_Ser405del |