HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160881818_160881819insGAGGT , CM000663.2:g.160881818_160881819insGAGGT | GRCh38 |
NC_000001.10:g.160851608_160851609insGAGGT , CM000663.1:g.160851608_160851609insGAGGT | GRCh37 |
NC_000001.9:g.159118232_159118233insGAGGT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326245.4:c.405+138_405+139insACCTC MANE Select | ENSP00000323587.3:n.405+138_405+139insACCTC | |
ENST00000326245.3:c.405+138_405+139insACCTC | ENSP00000323587.3:n.405+138_405+139insACCTC | |
ENST00000464077.1:n.339+138_339+139insACCTC | ||
NM_017625.2:c.405+138_405+139insACCTC | NP_060095.2:n.405+138_405+139insACCTC | |
NM_017625.3:c.405+138_405+139insACCTC MANE Select | NP_060095.2:n.405+138_405+139insACCTC |