Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134375484_134375485insT , CM000671.2:g.134375484_134375485insT | GRCh38 |
| NC_000009.11:g.137267330_137267331insT , CM000671.1:g.137267330_137267331insT | GRCh37 |
| NC_000009.10:g.136407151_136407152insT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000481739.2:c.29-26148_29-26147insT MANE Select | ENSP00000419692.1:n.29-26148_29-26147insT | |
| ENST00000356384.4:n.293+1354_293+1355insT | ||
| ENST00000481739.1:c.29-26148_29-26147insT | ENSP00000419692.1:n.29-26148_29-26147insT | |
| ENST00000484822.1:n.453-26148_453-26147insT | ||
| NM_002957.5:c.29-26148_29-26147insT | NP_002948.1:n.29-26148_29-26147insT | |
| NM_002957.6:c.29-26148_29-26147insT MANE Select | NP_002948.1:n.29-26148_29-26147insT |