Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584055_41584056insA , CM000679.2:g.41584055_41584056insA | GRCh38 |
| NC_000017.10:g.39740307_39740308insA , CM000679.1:g.39740307_39740308insA | GRCh37 |
| NC_000017.9:g.36993833_36993834insA | NCBI36 |
| NG_008624.1:g.7840_7841insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-135_766-134insT MANE Select | ENSP00000167586.6:n.766-135_766-134insT | |
| ENST00000167586.6:c.766-135_766-134insT | ENSP00000167586.6:n.766-135_766-134insT | |
| ENST00000476662.1:n.216-135_216-134insT | ||
| NM_000526.4:c.766-135_766-134insT | NP_000517.2:n.766-135_766-134insT | |
| NM_000526.5:c.766-135_766-134insT MANE Select | NP_000517.3:n.766-135_766-134insT |