Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.182838742dup , CM000664.2:g.182838742dup | GRCh38 |
| NC_000002.11:g.183703470dup , CM000664.1:g.183703470dup | GRCh37 |
| NC_000002.10:g.183411715dup | NCBI36 |
| NG_017197.1:g.33032dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295113.5:c.593-126dup MANE Select | ENSP00000295113.4:n.593-126dup | |
| ENST00000295113.4:c.593-126dup | ENSP00000295113.4:n.593-126dup | |
| NM_001463.3:c.593-126dup | NP_001454.2:n.593-126dup | |
| NM_001463.4:c.593-126dup MANE Select | NP_001454.2:n.593-126dup |