HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21176682_21176688delinsGTGCAAA , CM000674.2:g.21176682_21176688delinsGTGCAAA | GRCh38 |
NC_000012.11:g.21329616_21329622delinsGTGCAAA , CM000674.1:g.21329616_21329622delinsGTGCAAA | GRCh37 |
NC_000012.10:g.21220883_21220889delinsGTGCAAA | NCBI36 |
NG_011745.1:g.50489_50495delinsGTGCAAA , LRG_1022:g.50489_50495delinsGTGCAAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.360-94_360-88delinsGTGCAAA MANE Select | ENSP00000256958.2:n.360-94_360-88delinsGTGCAAA | |
ENST00000256958.2:c.360-94_360-88delinsGTGCAAA | ENSP00000256958.2:n.360-94_360-88delinsGTGCAAA | |
ENST00000543498.5:c.426-94_426-88delinsGTGCAAA | ||
NM_006446.4:c.360-94_360-88delinsGTGCAAA , LRG_1022t1:c.360-94_360-88delinsGTGCAAA | NP_006437.3:n.360-94_360-88delinsGTGCAAA | |
NM_006446.5:c.360-94_360-88delinsGTGCAAA MANE Select | NP_006437.3:n.360-94_360-88delinsGTGCAAA |