Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119422899_119422903del , CM000663.2:g.119422899_119422903del | GRCh38 |
| NC_000001.10:g.119965522_119965526del , CM000663.1:g.119965522_119965526del | GRCh37 |
| NC_000001.9:g.119767045_119767049del | NCBI36 |
| NG_013349.1:g.12969_12973del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369416.4:c.*279_*283del MANE Select | ENSP00000358424.3:n.*279_*283del | |
| ENST00000369416.3:c.*279_*283del | ENSP00000358424.3:n.*279_*283del | |
| ENST00000543831.5:c.*279_*283del | ENSP00000445122.1:n.*279_*283del | |
| NM_000198.3:c.*279_*283del | NP_000189.1:n.*279_*283del | |
| NM_001166120.1:c.*279_*283del | NP_001159592.1:n.*279_*283del | |
| NM_000198.4:c.*279_*283del MANE Select | NP_000189.1:n.*279_*283del | |
| NM_001166120.2:c.*279_*283del | NP_001159592.1:n.*279_*283del |