Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92645411T= , CM000672.2:g.92645411T= | GRCh38 |
| NC_000010.10:g.94405168T= , CM000672.1:g.94405168T= | GRCh37 |
| NC_000010.9:g.94395148T= | NCBI36 |
| NG_032580.1:g.57344T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260731.5:c.2316T= MANE Select | ENSP00000260731.3:p.Phe772= | |
| ENST00000676621.1:c.*834T= | ENSP00000503639.1:n.*834T= | |
| ENST00000676647.1:c.2109T= | ENSP00000503394.1:p.Phe703= | |
| ENST00000676757.1:c.2109T= | ENSP00000504289.1:p.Phe703= | |
| ENST00000677720.1:c.*290T= | ENSP00000504840.1:n.*290T= | |
| ENST00000260731.4:c.2316T= | ENSP00000260731.3:p.Phe772= | |
| NM_004523.3:c.2316T= | NP_004514.2:p.Phe772= | |
| NM_004523.4:c.2316T= MANE Select | NP_004514.2:p.Phe772= |