HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215571_21215572delinsCA , CM000674.2:g.21215571_21215572delinsCA | GRCh38 |
NC_000012.11:g.21368505_21368506delinsCA , CM000674.1:g.21368505_21368506delinsCA | GRCh37 |
NC_000012.10:g.21259772_21259773delinsCA | NCBI36 |
NG_011745.1:g.89378_89379delinsCA , LRG_1022:g.89378_89379delinsCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1548_1498-1547delinsCA MANE Select | ENSP00000256958.2:n.1498-1548_1498-1547delinsCA | |
ENST00000256958.2:c.1498-1548_1498-1547delinsCA | ENSP00000256958.2:n.1498-1548_1498-1547delinsCA | |
NM_006446.4:c.1498-1548_1498-1547delinsCA , LRG_1022t1:c.1498-1548_1498-1547delinsCA | NP_006437.3:n.1498-1548_1498-1547delinsCA | |
NM_006446.5:c.1498-1548_1498-1547delinsCA MANE Select | NP_006437.3:n.1498-1548_1498-1547delinsCA |