Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.40866610_40866611delinsGA , CM000679.2:g.40866610_40866611delinsGA | GRCh38 |
| NC_000017.10:g.39022862_39022863delinsGA , CM000679.1:g.39022862_39022863delinsGA | GRCh37 |
| NC_000017.9:g.36276388_36276389delinsGA | NCBI36 |
| NG_008077.1:g.5600_5601delinsTC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251643.5:c.567+9_567+10delinsTC MANE Select | ENSP00000251643.4:n.567+9_567+10delinsTC | |
| ENST00000647902.1:c.459+9_459+10delinsTC | ENSP00000497770.1:n.459+9_459+10delinsTC | |
| ENST00000251643.4:c.567+9_567+10delinsTC | ENSP00000251643.4:n.567+9_567+10delinsTC | |
| NM_000223.3:c.567+9_567+10delinsTC | NP_000214.1:n.567+9_567+10delinsTC | |
| XR_934754.1:n.1500+15750_1500+15751delinsGA | ||
| XR_934754.2:n.2008+15750_2008+15751delinsGA | ||
| NM_000223.4:c.567+9_567+10delinsTC MANE Select | NP_000214.1:n.567+9_567+10delinsTC |