Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.74774562_74774564del , CM000678.2:g.74774562_74774564del | GRCh38 |
| NC_000016.9:g.74808460_74808462del , CM000678.1:g.74808460_74808462del | GRCh37 |
| NC_000016.8:g.73365961_73365963del | NCBI36 |
| NG_017070.1:g.5273_5275del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219368.8:c.197_199del MANE Select | ENSP00000219368.3:p.Pro66del | |
| ENST00000219368.7:c.197_199del | ENSP00000219368.3:p.Pro66del | |
| ENST00000567683.5:c.197_199del | ENSP00000455126.1:p.Pro66del | |
| NM_024306.4:c.197_199del | NP_077282.3:p.Pro66del | |
| XM_011523317.1:c.197_199del | XP_011521619.1:p.Pro66del | |
| XM_011523318.1:c.197_199del | XP_011521620.1:p.Pro66del | |
| XM_011523317.3:c.197_199del | XP_011521619.1:p.Pro66del | |
| NM_024306.5:c.197_199del MANE Select | NP_077282.3:p.Pro66del |