Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965803_37965805del , CM000670.2:g.37965803_37965805del | GRCh38 |
| NC_000008.10:g.37823321_37823323del , CM000670.1:g.37823321_37823323del | GRCh37 |
| NC_000008.9:g.37942478_37942480del | NCBI36 |
| NG_011936.1:g.5864_5866del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000345060.5:c.667_669del MANE Select | ENSP00000343782.3:p.Val223del | |
| ENST00000520341.2:n.795_797del | ||
| ENST00000647937.1:c.151_153del | ENSP00000497740.1:p.Val51del | |
| ENST00000345060.4:c.667_669del | ENSP00000343782.3:p.Val223del | |
| ENST00000614635.1:c.667_669del | ENSP00000480325.1:p.Val223del | |
| NM_000025.2:c.667_669del | NP_000016.1:p.Val223del | |
| NM_000025.3:c.667_669del MANE Select | NP_000016.1:p.Val223del |