Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612625_41612636del , CM000679.2:g.41612625_41612636del | GRCh38 |
| NC_000017.10:g.39768877_39768888del , CM000679.1:g.39768877_39768888del | GRCh37 |
| NC_000017.9:g.37022403_37022414del | NCBI36 |
| NG_008301.1:g.5202_5213del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.63_74del MANE Select | ENSP00000301653.3:p.Gly22_Gly25del | |
| ENST00000301653.8:c.63_74del | ENSP00000301653.3:p.Gly22_Gly25del | |
| ENST00000588319.1:n.140_151del | ||
| ENST00000590990.1:c.63_74del | ENSP00000467105.1:p.Gly22_Gly25del | |
| ENST00000593067.1:c.-313+164_-313+175del | ENSP00000467124.1:n.-313+164_-313+175del | |
| NM_005557.3:c.63_74del | NP_005548.2:p.Gly22_Gly25del | |
| NM_005557.4:c.63_74del MANE Select | NP_005548.2:p.Gly22_Gly25del |