Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5232983A= , CM000673.2:g.5232983A= | GRCh38 |
| NC_000011.9:g.5254213A= , CM000673.1:g.5254213A= | GRCh37 |
| NC_000011.8:g.5210789A= | NCBI36 |
| NG_000007.3:g.64633T= | |
| NG_063112.2:g.15675T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000519.4:c.425T= MANE Select | NP_000510.1:p.Leu142= |
| ENST00000650601.1:c.425T= MANE Select | ENSP00000497529.1:p.Leu142= |
| NM_000519.3:c.425T= | NP_000510.1:p.Leu142= |
| ENST00000292901.7:c.316-185T= | ENSP00000292901.3:n.316-185T= |
| ENST00000380299.3:c.425T= | ENSP00000369654.3:p.Leu142= |
| ENST00000417377.1:c.202T= | ENSP00000414741.1:p.Trp68= |
| ENST00000643122.1:c.425T= | ENSP00000494708.1:p.Leu142= |