Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.75210907dup , CM000680.2:g.75210907dup | GRCh38 |
| NC_000018.9:g.72922862dup , CM000680.1:g.72922862dup | GRCh37 |
| NC_000018.8:g.71051850dup | NCBI36 |
| NG_032047.1:g.5153dup |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001308210.2:c.-970dup MANE Select | NP_001295139.1:n.-970dup |
| ENST00000580243.3:c.-970dup MANE Select | ENSP00000464391.1:n.-970dup |
| NM_005786.5:c.-432dup | NP_005777.3:n.-432dup |
| NM_005786.6:c.-432dup | NP_005777.3:n.-432dup |
| ENST00000322038.5:c.-432dup | ENSP00000323584.5:n.-432dup |