Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74919463T= , CM000679.2:g.74919463T= | GRCh38 |
| NC_000017.10:g.72915558T= , CM000679.1:g.72915558T= | GRCh37 |
| NC_000017.9:g.70427153T= | NCBI36 |
| NG_007882.1:g.8794A= | |
| NG_033062.1:g.189T= | |
| NG_007882.2:g.8801A= | |
| NG_033062.2:g.189T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_173477.5:c.1373A= MANE Select | NP_775748.2:p.Asp458= |
| ENST00000614341.5:c.1373A= MANE Select | ENSP00000480279.1:p.Asp458= |
| NM_001282489.2:c.1064A= | NP_001269418.1:p.Asp355= |
| NM_001282489.3:c.1064A= | NP_001269418.1:p.Asp355= |
| NM_173477.4:c.1373A= | NP_775748.2:p.Asp458= |
| ENST00000579243.1:c.*972A= | ENSP00000462568.1:n.*972A= |
| ENST00000614341.4:c.1373A= | ENSP00000480279.1:p.Asp458= |
| XM_011524296.1:c.1064A= | XP_011522598.1:p.Asp355= |
| XM_011524296.2:c.1064A= | XP_011522598.1:p.Asp355= |