Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14871336dup , CM000667.2:g.14871336dup | GRCh38 |
| NC_000005.9:g.14871445dup , CM000667.1:g.14871445dup | GRCh37 |
| NC_000005.8:g.14924445dup | NCBI36 |
| NG_008273.1:g.5443dup | |
| NG_008273.2:g.5450dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.96+16dup MANE Select | ENSP00000284268.6:n.96+16dup | |
| ENST00000284268.6:c.96+16dup | ENSP00000284268.6:n.96+16dup | |
| ENST00000505140.1:c.112dup | ENSP00000426332.1:p.Ala38GlyfsTer? | |
| ENST00000513115.1:n.121+16dup | ||
| NM_054027.4:c.96+16dup | NP_473368.1:n.96+16dup | |
| XM_011514067.1:c.96+16dup | XP_011512369.1:n.96+16dup | |
| NM_054027.5:c.96+16dup | NP_473368.1:n.96+16dup | |
| NM_054027.6:c.96+16dup MANE Select | NP_473368.1:n.96+16dup |