HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1423713_1423715delinsACT , CM000667.2:g.1423713_1423715delinsACT | GRCh38 |
NC_000005.9:g.1423828_1423830delinsACT , CM000667.1:g.1423828_1423830delinsACT | GRCh37 |
NC_000005.8:g.1476828_1476830delinsACT | NCBI36 |
NG_015885.1:g.26714_26716delinsAGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.654-1701_654-1699delinsAGT MANE Select | ENSP00000270349.9:n.654-1701_654-1699delinsAGT | |
ENST00000270349.11:c.654-1701_654-1699delinsAGT | ENSP00000270349.9:n.654-1701_654-1699delinsAGT | |
NM_001044.4:c.654-1701_654-1699delinsAGT | NP_001035.1:n.654-1701_654-1699delinsAGT | |
NM_001044.5:c.654-1701_654-1699delinsAGT MANE Select | NP_001035.1:n.654-1701_654-1699delinsAGT |