Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68431381_68431382del , CM000663.2:g.68431381_68431382del | GRCh38 |
| NC_000001.10:g.68897064_68897065del , CM000663.1:g.68897064_68897065del | GRCh37 |
| NC_000001.9:g.68669652_68669653del | NCBI36 |
| NG_008472.1:g.23578_23579del | |
| NG_008472.2:g.23578_23579del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1244-6_1244-5del MANE Select | ENSP00000262340.5:n.1244-6_1244-5del | |
| ENST00000262340.5:c.1244-6_1244-5del | ENSP00000262340.5:n.1244-6_1244-5del | |
| NM_000329.2:c.1244-6_1244-5del | NP_000320.1:n.1244-6_1244-5del | |
| XM_017002027.1:c.968-6_968-5del | XP_016857516.1:n.968-6_968-5del | |
| NM_000329.3:c.1244-6_1244-5del MANE Select | NP_000320.1:n.1244-6_1244-5del |