Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63942031_63942032delinsAG , CM000679.2:g.63942031_63942032delinsAG | GRCh38 |
| NC_000017.10:g.62019391_62019392delinsAG , CM000679.1:g.62019391_62019392delinsAG | GRCh37 |
| NC_000017.9:g.59373123_59373124delinsAG | NCBI36 |
| NG_011699.1:g.35887_35888delinsCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.4289-39_4289-38delinsCT MANE Select | ENSP00000396320.1:n.4289-39_4289-38delinsCT | |
| ENST00000578147.5:c.4289-39_4289-38delinsCT | ENSP00000463963.1:n.4289-39_4289-38delinsCT | |
| NM_000334.4:c.4289-39_4289-38delinsCT MANE Select | NP_000325.4:n.4289-39_4289-38delinsCT | |
| XM_005257566.3:c.4289-39_4289-38delinsCT | XP_005257623.1:n.4289-39_4289-38delinsCT |