Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45094655G>A , CM000677.2:g.45094655G>A | GRCh38 |
| NC_000015.9:g.45386853G>A , CM000677.1:g.45386853G>A | GRCh37 |
| NC_000015.8:g.43174145G>A | NCBI36 |
| NG_009447.1:g.24507C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001363711.2:c.4432C>T MANE Select | NP_001350640.1:p.Arg1478Trp |
| ENST00000389039.11:c.4432C>T MANE Select | ENSP00000373691.7:p.Arg1478Trp |
| NM_001363711.1:c.4432C>T | NP_001350640.1:p.Arg1478Trp |
| NM_014080.4:c.4432C>T | NP_054799.4:p.Arg1478Trp |
| NM_014080.5:c.4432C>T | NP_054799.4:p.Arg1478Trp |
| ENST00000389039.10:c.4432C>T | ENSP00000373691.6:p.Arg1478Trp |
| ENST00000603300.1:c.4432C>T | ENSP00000475084.1:p.Arg1478Trp |
| XM_005254421.2:c.4432C>T | XP_005254478.1:p.Arg1478Trp |