Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147132392G>A , CM000669.2:g.147132392G>A | GRCh38 |
| NC_000007.13:g.146829484G>A , CM000669.1:g.146829484G>A | GRCh37 |
| NC_000007.12:g.146460417G>A | NCBI36 |
| NG_007092.2:g.1021032G>A | |
| NG_007092.3:g.1021392G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.1231G>A MANE Select | ENSP00000354778.3:p.Val411Ile | |
| ENST00000636561.1:n.1134G>A | ||
| ENST00000636870.1:n.1093G>A | ||
| ENST00000637150.1:n.1160G>A | ||
| ENST00000637694.1:n.1134G>A | ||
| ENST00000637825.1:n.714G>A | ||
| ENST00000638117.1:n.1134G>A | ||
| ENST00000361727.7:c.1231G>A | ENSP00000354778.3:p.Val411Ile | |
| NM_014141.5:c.1231G>A | NP_054860.1:p.Val411Ile | |
| XM_017011950.2:c.1231G>A | XP_016867439.1:p.Val411Ile | |
| NM_014141.6:c.1231G>A MANE Select | NP_054860.1:p.Val411Ile |