Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.93998136_93998137del , CM000663.2:g.93998136_93998137del | GRCh38 |
| NC_000001.10:g.94463692_94463693del , CM000663.1:g.94463692_94463693del | GRCh37 |
| NC_000001.9:g.94236280_94236281del | NCBI36 |
| NG_009073.1:g.128013_128014del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6480-27_6480-26del MANE Select | ENSP00000359245.3:n.6480-27_6480-26del | |
| ENST00000370225.3:c.6480-27_6480-26del | ENSP00000359245.3:n.6480-27_6480-26del | |
| ENST00000536513.5:c.2856-27_2856-26del | ENSP00000439707.2:n.2856-27_2856-26del | |
| NM_000350.2:c.6480-27_6480-26del | NP_000341.2:n.6480-27_6480-26del | |
| NM_000350.3:c.6480-27_6480-26del MANE Select | NP_000341.2:n.6480-27_6480-26del |