HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215650_21215655delinsGTTGGT , CM000674.2:g.21215650_21215655delinsGTTGGT | GRCh38 |
NC_000012.11:g.21368584_21368589delinsGTTGGT , CM000674.1:g.21368584_21368589delinsGTTGGT | GRCh37 |
NC_000012.10:g.21259851_21259856delinsGTTGGT | NCBI36 |
NG_011745.1:g.89457_89462delinsGTTGGT , LRG_1022:g.89457_89462delinsGTTGGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1469_1498-1464delinsGTTGGT MANE Select | ENSP00000256958.2:n.1498-1469_1498-1464de... | |
ENST00000256958.2:c.1498-1469_1498-1464delinsGTTGGT | ENSP00000256958.2:n.1498-1469_1498-1464de... | |
NM_006446.4:c.1498-1469_1498-1464delinsGTTGGT , LRG_1022t1:c.1498-1469_1498-1464delinsGTTGGT | NP_006437.3:n.1498-1469_1498-1464delinsGT... | |
NM_006446.5:c.1498-1469_1498-1464delinsGTTGGT MANE Select | NP_006437.3:n.1498-1469_1498-1464delinsGT... |