Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63971179_63971180delinsGT , CM000679.2:g.63971179_63971180delinsGT | GRCh38 |
| NC_000017.10:g.62048539_62048540delinsGT , CM000679.1:g.62048539_62048540delinsGT | GRCh37 |
| NC_000017.9:g.59402271_59402272delinsGT | NCBI36 |
| NG_011699.1:g.6739_6740delinsAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.685_686delinsAC MANE Select | ENSP00000396320.1:p.Thr229= | |
| ENST00000578147.5:c.685_686delinsAC | ENSP00000463963.1:p.Thr229= | |
| NM_000334.4:c.685_686delinsAC MANE Select | NP_000325.4:p.Thr229= | |
| XM_005257566.3:c.685_686delinsAC | XP_005257623.1:p.Thr229= |