Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584065_41584071delinsCTCTCTT , CM000679.2:g.41584065_41584071delinsCTCTCTT | GRCh38 |
| NC_000017.10:g.39740317_39740323delinsCTCTCTT , CM000679.1:g.39740317_39740323delinsCTCTCTT | GRCh37 |
| NC_000017.9:g.36993843_36993849delinsCTCTCTT | NCBI36 |
| NG_008624.1:g.7825_7831delinsAAGAGAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-150_766-144delinsAAGAGAG MANE Select | ENSP00000167586.6:n.766-150_766-144delinsAAGAGAG | |
| ENST00000167586.6:c.766-150_766-144delinsAAGAGAG | ENSP00000167586.6:n.766-150_766-144delinsAAGAGAG | |
| ENST00000476662.1:n.216-150_216-144delinsAAGAGAG | ||
| NM_000526.4:c.766-150_766-144delinsAAGAGAG | NP_000517.2:n.766-150_766-144delinsAAGAGAG | |
| NM_000526.5:c.766-150_766-144delinsAAGAGAG MANE Select | NP_000517.3:n.766-150_766-144delinsAAGAGAG |