Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.40099101_40099105dup , CM000679.2:g.40099101_40099105dup | GRCh38 |
| NC_000017.10:g.38255354_38255358dup , CM000679.1:g.38255354_38255358dup | GRCh37 |
| NC_000017.9:g.35508880_35508884dup | NCBI36 |
| NG_033084.1:g.6625_6629dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000246672.4:c.31+963_31+967dup MANE Select | ENSP00000246672.3:n.31+963_31+967dup | |
| ENST00000246672.3:c.31+963_31+967dup | ENSP00000246672.3:n.31+963_31+967dup | |
| NM_021724.4:c.31+963_31+967dup | NP_068370.1:n.31+963_31+967dup | |
| NM_021724.5:c.31+963_31+967dup MANE Select | NP_068370.1:n.31+963_31+967dup |