Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17126762T= , CM000672.2:g.17126762T= | GRCh38 |
| NC_000010.10:g.17168761T= , CM000672.1:g.17168761T= | GRCh37 |
| NC_000010.9:g.17208767T= | NCBI36 |
| NG_008967.1:g.8056A= , LRG_540:g.8056A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377833.10:c.386A= MANE Select | ENSP00000367064.4:p.Gln129= | |
| ENST00000377823.1:c.386A= | ENSP00000367054.1:p.Gln129= | |
| ENST00000377833.8:c.386A= | ENSP00000367064.4:p.Gln129= | |
| ENST00000433666.5:c.47A= | ENSP00000415970.1:p.Gln16= | |
| NM_001081.3:c.386A= , LRG_540t1:c.386A= | NP_001072.2:p.Gln129= | |
| XM_011519708.1:c.386A= | XP_011518010.1:p.Gln129= | |
| XM_011519708.2:c.386A= | XP_011518010.1:p.Gln129= | |
| NM_001081.4:c.386A= MANE Select | NP_001072.2:p.Gln129= |