Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1610418_1610424dup , CM000668.2:g.1610418_1610424dup | GRCh38 |
| NC_000006.11:g.1610653_1610659dup , CM000668.1:g.1610653_1610659dup | GRCh37 |
| NC_000006.10:g.1555652_1555658dup | NCBI36 |
| NG_009368.1:g.4973_4979dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000645831.2:c.-28_-22dup MANE Select | ENSP00000493906.1:n.-28_-22dup | |
| ENST00000380874.3:c.-28_-22dup | ENSP00000370256.2:n.-28_-22dup | |
| NM_001453.3:c.-28_-22dup MANE Select | NP_001444.2:n.-28_-22dup |