Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.41173768T= , CM000684.2:g.41173768T= | GRCh38 |
| NC_000022.10:g.41569772T= , CM000684.1:g.41569772T= | GRCh37 |
| NC_000022.9:g.39899718T= | NCBI36 |
| NG_009817.1:g.86159T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001429.4:c.4763T= MANE Select | NP_001420.2:p.Met1588= |
| ENST00000263253.9:c.4763T= MANE Select | ENSP00000263253.7:p.Met1588= |
| NM_001362843.1:c.4685T= | NP_001349772.1:p.Met1562= |
| NM_001362843.2:c.4685T= | NP_001349772.1:p.Met1562= |
| NM_001429.3:c.4763T= | NP_001420.2:p.Met1588= |
| ENST00000263253.8:c.4763T= | ENSP00000263253.7:p.Met1588= |
| ENST00000674155.1:c.4685T= | ENSP00000501078.1:p.Met1562= |
| ENST00000703544.1:c.*2683T= | ENSP00000515365.1:n.*2683T= |
| XM_006724165.2:c.4685T= | XP_006724228.1:p.Met1562= |