Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23421106dup , CM000676.2:g.23421106dup | GRCh38 |
| NC_000014.8:g.23890315dup , CM000676.1:g.23890315dup | GRCh37 |
| NC_000014.7:g.22960155dup | NCBI36 |
| NG_007884.1:g.19556dup , LRG_384:g.19556dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.3246-58dup MANE Select | ENSP00000347507.3:n.3246-58dup | |
| ENST00000355349.3:c.3246-58dup | ENSP00000347507.3:n.3246-58dup | |
| NM_000257.3:c.3246-58dup | NP_000248.2:n.3246-58dup | |
| XR_245686.3:n.3354-58dup | ||
| XM_017021340.1:c.3246-58dup | XP_016876829.1:n.3246-58dup | |
| NM_000257.4:c.3246-58dup MANE Select | NP_000248.2:n.3246-58dup |