Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951959dup , CM000670.2:g.19951959dup | GRCh38 |
| NC_000008.10:g.19809470dup , CM000670.1:g.19809470dup | GRCh37 |
| NC_000008.9:g.19853750dup | NCBI36 |
| NG_008855.1:g.17889dup | |
| NG_008855.2:g.55243dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.429+11dup MANE Select | ENSP00000497642.1:n.429+11dup | |
| ENST00000311322.8:c.429+11dup | ENSP00000309757.6:n.429+11dup | |
| ENST00000520959.5:c.201+11dup | ENSP00000428496.1:n.201+11dup | |
| NM_000237.2:c.429+11dup | NP_000228.1:n.429+11dup | |
| NM_000237.3:c.429+11dup MANE Select | NP_000228.1:n.429+11dup |