Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990407_45990415del , CM000683.2:g.45990407_45990415del | GRCh38 |
| NC_000021.8:g.47410321_47410329del , CM000683.1:g.47410321_47410329del | GRCh37 |
| NC_000021.7:g.46234749_46234757del | NCBI36 |
| NG_008674.1:g.13659_13667del , LRG_475:g.13659_13667del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.987_995del MANE Select | ENSP00000355180.3:p.Val330_Gly332del | |
| ENST00000361866.7:c.987_995del | ENSP00000355180.3:p.Val330_Gly332del | |
| ENST00000612273.1:c.987_995del | ENSP00000483630.1:p.Val330_Gly332del | |
| NM_001848.2:c.987_995del , LRG_475t1:c.987_995del | NP_001839.2:p.Val330_Gly332del | |
| NM_001848.3:c.987_995del MANE Select | NP_001839.2:p.Val330_Gly332del |