Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133638649_133638650dup , CM000671.2:g.133638649_133638650dup | GRCh38 |
| NC_000009.11:g.136503771_136503772dup , CM000671.1:g.136503771_136503772dup | GRCh37 |
| NC_000009.10:g.135493592_135493593dup | NCBI36 |
| NG_008645.1:g.7287_7288dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263611.3:c.333+1939_333+1940dup | ENSP00000263611.3:n.333+1939_333+1940dup | |
| ENST00000393056.8:c.340-1197_340-1196dup MANE Select | ENSP00000376776.2:n.340-1197_340-1196dup | |
| ENST00000263611.2:c.297+1939_297+1940dup | ENSP00000263611.2:n.297+1939_297+1940dup | |
| ENST00000393056.6:c.340-1197_340-1196dup | ENSP00000376776.2:n.340-1197_340-1196dup | |
| NM_000787.3:c.340-1197_340-1196dup | NP_000778.3:n.340-1197_340-1196dup | |
| NM_000787.4:c.340-1197_340-1196dup MANE Select | NP_000778.3:n.340-1197_340-1196dup |