Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1415426_1415427insT , CM000667.2:g.1415426_1415427insT | GRCh38 |
| NC_000005.9:g.1415541_1415542insT , CM000667.1:g.1415541_1415542insT | GRCh37 |
| NC_000005.8:g.1468541_1468542insT | NCBI36 |
| NG_015885.1:g.35002_35003insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1032-612_1032-611insA MANE Select | ENSP00000270349.9:n.1032-612_1032-611insA | |
| ENST00000270349.11:c.1032-612_1032-611insA | ENSP00000270349.9:n.1032-612_1032-611insA | |
| ENST00000511750.1:n.482-612_482-611insA | ||
| NM_001044.4:c.1032-612_1032-611insA | NP_001035.1:n.1032-612_1032-611insA | |
| NM_001044.5:c.1032-612_1032-611insA MANE Select | NP_001035.1:n.1032-612_1032-611insA |