Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81493845dup , CM000665.2:g.81493845dup | GRCh38 |
| NC_000003.11:g.81542996dup , CM000665.1:g.81542996dup | GRCh37 |
| NC_000003.10:g.81625686dup | NCBI36 |
| NG_011810.1:g.272966dup |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000158.4:c.2053-3372dup MANE Select | NP_000149.4:n.2053-3372dup |
| ENST00000429644.7:c.2053-3372dup MANE Select | ENSP00000410833.2:n.2053-3372dup |
| NM_000158.3:c.2053-3372dup | NP_000149.3:n.2053-3372dup |
| ENST00000429644.6:c.2053-3372dup | ENSP00000410833.2:n.2053-3372dup |
| ENST00000489715.1:c.1930-3372dup | ENSP00000419638.1:n.1930-3372dup |