Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68438123_68438125del , CM000663.2:g.68438123_68438125del | GRCh38 |
| NC_000001.10:g.68903806_68903808del , CM000663.1:g.68903806_68903808del | GRCh37 |
| NC_000001.9:g.68676394_68676396del | NCBI36 |
| NG_008472.1:g.16839_16841del | |
| NG_008472.2:g.16839_16841del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1128+66_1128+68del MANE Select | ENSP00000262340.5:n.1128+66_1128+68del | |
| ENST00000262340.5:c.1128+66_1128+68del | ENSP00000262340.5:n.1128+66_1128+68del | |
| NM_000329.2:c.1128+66_1128+68del | NP_000320.1:n.1128+66_1128+68del | |
| XM_017002027.1:c.852+66_852+68del | XP_016857516.1:n.852+66_852+68del | |
| NM_000329.3:c.1128+66_1128+68del MANE Select | NP_000320.1:n.1128+66_1128+68del |