Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20188848T= , CM000675.2:g.20188848T= | GRCh38 |
| NC_000013.10:g.20762987T= , CM000675.1:g.20762987T= | GRCh37 |
| NC_000013.9:g.19660987T= | NCBI36 |
| NG_008358.1:g.9128A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.*53A= | ENSP00000372295.1:n.*53A= | |
| ENST00000382848.5:c.*53A= MANE Select | ENSP00000372299.4:n.*53A= | |
| ENST00000382844.1:c.*53A= | ENSP00000372295.1:n.*53A= | |
| ENST00000382848.4:c.*53A= | ENSP00000372299.4:n.*53A= | |
| NM_004004.5:c.*53A= | NP_003995.2:n.*53A= | |
| XM_011535049.1:c.*53A= | XP_011533351.1:n.*53A= | |
| XM_011535049.2:c.*53A= | XP_011533351.1:n.*53A= | |
| NM_004004.6:c.*53A= MANE Select | NP_003995.2:n.*53A= |