Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63944531_63944532delinsTG , CM000679.2:g.63944531_63944532delinsTG | GRCh38 |
| NC_000017.10:g.62021891_62021892delinsTG , CM000679.1:g.62021891_62021892delinsTG | GRCh37 |
| NC_000017.9:g.59375623_59375624delinsTG | NCBI36 |
| NG_011699.1:g.33387_33388delinsCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.3912+141_3912+142delinsCA MANE Select | ENSP00000396320.1:n.3912+141_3912+142delinsCA | |
| ENST00000578147.5:c.3916+137_3916+138delinsCA | ENSP00000463963.1:n.3916+137_3916+138delinsCA | |
| NM_000334.4:c.3912+141_3912+142delinsCA MANE Select | NP_000325.4:n.3912+141_3912+142delinsCA | |
| XM_005257566.3:c.3912+141_3912+142delinsCA | XP_005257623.1:n.3912+141_3912+142delinsCA |