Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.159884352dup , CM000663.2:g.159884352dup | GRCh38 |
| NC_000001.10:g.159854142dup , CM000663.1:g.159854142dup | GRCh37 |
| NC_000001.9:g.158120766dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368099.9:c.897+84dup MANE Select | ENSP00000357079.4:n.897+84dup | |
| ENST00000368099.8:c.897+84dup | ENSP00000357079.4:n.897+84dup | |
| ENST00000426543.6:c.642+84dup | ENSP00000403044.2:n.642+84dup | |
| ENST00000476696.5:c.897+84dup | ENSP00000483972.1:n.897+84dup | |
| NM_012337.2:c.897+84dup | NP_036469.2:n.897+84dup | |
| NM_012337.3:c.897+84dup MANE Select | NP_036469.2:n.897+84dup |