Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.129209348G= , CM000669.2:g.129209348G= | GRCh38 |
| NC_000007.13:g.128849189G= , CM000669.1:g.128849189G= | GRCh37 |
| NC_000007.12:g.128636425G= | NCBI36 |
| NG_023340.1:g.25477G= | |
| NG_023340.2:g.25477G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005631.5:c.1417G= MANE Select | NP_005622.1:p.Asp473= |
| ENST00000249373.8:c.1417G= MANE Select | ENSP00000249373.3:p.Asp473= |
| NM_005631.4:c.1417G= | NP_005622.1:p.Asp473= |
| ENST00000249373.7:c.1417G= | ENSP00000249373.3:p.Asp473= |
| ENST00000462420.2:c.437+497G= | |
| ENST00000655644.1:c.*1221+497G= | ENSP00000499377.1:n.*1221+497G= |
| XM_011516522.1:c.1027G= | XP_011514824.1:p.Asp343= |
| XM_024446891.1:c.1027G= | XP_024302659.1:p.Asp343= |