Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119753287A= , CM000663.2:g.119753287A= | GRCh38 |
| NC_000001.10:g.120295910A= , CM000663.1:g.120295910A= | GRCh37 |
| NC_000001.9:g.120097433A= | NCBI36 |
| NG_013348.1:g.20646T= , LRG_447:g.20646T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369406.8:c.1287T= MANE Select | ENSP00000358414.3:p.Ala429= | |
| ENST00000369406.7:c.1287T= | ENSP00000358414.3:p.Ala429= | |
| ENST00000544913.2:c.1161T= | ENSP00000439495.2:p.Ala387= | |
| NM_001166107.1:c.1161T= , LRG_447t2:c.1161T= | NP_001159579.1:p.Ala387= | |
| NM_005518.3:c.1287T= , LRG_447t1:c.1287T= | NP_005509.1:p.Ala429= | |
| XM_011541313.1:c.1122T= | XP_011539615.1:p.Ala374= | |
| XM_011541313.2:c.1122T= | XP_011539615.1:p.Ala374= | |
| NM_005518.4:c.1287T= MANE Select | NP_005509.1:p.Ala429= |