Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68431284dup , CM000663.2:g.68431284dup | GRCh38 |
| NC_000001.10:g.68896967dup , CM000663.1:g.68896967dup | GRCh37 |
| NC_000001.9:g.68669555dup | NCBI36 |
| NG_008472.1:g.23676dup | |
| NG_008472.2:g.23676dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1336dup MANE Select | ENSP00000262340.5:p.Arg446LysfsTer4 | |
| ENST00000262340.5:c.1336dup | ENSP00000262340.5:p.Arg446LysfsTer4 | |
| NM_000329.2:c.1336dup | NP_000320.1:p.Arg446LysfsTer4 | |
| XM_017002027.1:c.1060dup | XP_016857516.1:p.Arg354LysfsTer4 | |
| NM_000329.3:c.1336dup MANE Select | NP_000320.1:p.Arg446LysfsTer4 |