HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215745_21215748delinsCCTT , CM000674.2:g.21215745_21215748delinsCCTT | GRCh38 |
NC_000012.11:g.21368679_21368682delinsCCTT , CM000674.1:g.21368679_21368682delinsCCTT | GRCh37 |
NC_000012.10:g.21259946_21259949delinsCCTT | NCBI36 |
NG_011745.1:g.89552_89555delinsCCTT , LRG_1022:g.89552_89555delinsCCTT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1374_1498-1371delinsCCTT MANE Select | ENSP00000256958.2:n.1498-1374_1498-1371de... | |
ENST00000256958.2:c.1498-1374_1498-1371delinsCCTT | ENSP00000256958.2:n.1498-1374_1498-1371de... | |
NM_006446.4:c.1498-1374_1498-1371delinsCCTT , LRG_1022t1:c.1498-1374_1498-1371delinsCCTT | NP_006437.3:n.1498-1374_1498-1371delinsCC... | |
NM_006446.5:c.1498-1374_1498-1371delinsCCTT MANE Select | NP_006437.3:n.1498-1374_1498-1371delinsCC... |