Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38146194_38146220del , CM000670.2:g.38146194_38146220del | GRCh38 |
| NC_000008.10:g.38003712_38003738del , CM000670.1:g.38003712_38003738del | GRCh37 |
| NC_000008.9:g.38122869_38122895del | NCBI36 |
| NG_011827.1:g.9863_9889del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.465+69_466-47del MANE Select | ENSP00000276449.3:n.465+69_466-47del | |
| ENST00000276449.8:c.465+69_466-47del | ENSP00000276449.3:n.465+69_466-47del | |
| ENST00000520114.1:n.952+69_953-47del | ||
| ENST00000522050.1:c.401+69_402-47del | ||
| NM_000349.2:c.465+69_466-47del | NP_000340.2:n.465+69_466-47del | |
| XM_006716392.1:c.465+69_466-47del | XP_006716455.1:n.465+69_466-47del | |
| NM_000349.3:c.465+69_466-47del MANE Select | NP_000340.2:n.465+69_466-47del |