Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.90918986_90918987insT , CM000672.2:g.90918986_90918987insT | GRCh38 |
| NC_000010.10:g.92678743_92678744insT , CM000672.1:g.92678743_92678744insT | GRCh37 |
| NC_000010.9:g.92668723_92668724insT | NCBI36 |
| NG_023227.1:g.7289_7290insA , LRG_379:g.7289_7290insA |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014391.3:c.346-15_346-14insA MANE Select | NP_055206.2:n.346-15_346-14insA |
| ENST00000371697.4:c.346-15_346-14insA MANE Select | ENSP00000360762.3:n.346-15_346-14insA |
| NM_014391.2:c.346-15_346-14insA , LRG_379t1:c.346-15_346-14insA | NP_055206.2:n.346-15_346-14insA |
| ENST00000371697.3:c.346-15_346-14insA | ENSP00000360762.3:n.346-15_346-14insA |