Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.856209_856221dup , CM000681.2:g.856209_856221dup | GRCh38 |
| NC_000019.9:g.856209_856221dup , CM000681.1:g.856209_856221dup | GRCh37 |
| NC_000019.8:g.807209_807221dup | NCBI36 |
| NG_007274.1:g.1545_1557dup , LRG_46:g.1545_1557dup | |
| NG_009627.1:g.8919_8931dup , LRG_57:g.8919_8931dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263621.2:c.*45_*57dup MANE Select | ENSP00000263621.1:n.*45_*57dup | |
| ENST00000263621.1:c.*45_*57dup | ENSP00000263621.1:n.*45_*57dup | |
| ENST00000590230.5:c.*45_*57dup | ENSP00000466090.1:n.*45_*57dup | |
| NM_001972.2:c.*45_*57dup , LRG_57t1:c.*45_*57dup | NP_001963.1:n.*45_*57dup | |
| XM_011527775.1:c.*45_*57dup | XP_011526077.1:n.*45_*57dup | |
| XM_011527776.1:c.*45_*57dup | XP_011526078.1:n.*45_*57dup | |
| NM_001972.3:c.*45_*57dup | NP_001963.1:n.*45_*57dup | |
| NM_001972.4:c.*45_*57dup MANE Select | NP_001963.1:n.*45_*57dup |