HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21196814_21196815delinsCA , CM000674.2:g.21196814_21196815delinsCA | GRCh38 |
NC_000012.11:g.21349748_21349749delinsCA , CM000674.1:g.21349748_21349749delinsCA | GRCh37 |
NC_000012.10:g.21241015_21241016delinsCA | NCBI36 |
NG_011745.1:g.70621_70622delinsCA , LRG_1022:g.70621_70622delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.728-132_728-131delinsCA MANE Select | ENSP00000256958.2:n.728-132_728-131delinsCA | |
ENST00000256958.2:c.728-132_728-131delinsCA | ENSP00000256958.2:n.728-132_728-131delinsCA | |
NM_006446.4:c.728-132_728-131delinsCA , LRG_1022t1:c.728-132_728-131delinsCA | NP_006437.3:n.728-132_728-131delinsCA | |
NM_006446.5:c.728-132_728-131delinsCA MANE Select | NP_006437.3:n.728-132_728-131delinsCA |