HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10658397_10658398insGGCTAT , CM000682.2:g.10658397_10658398insGGCTAT | GRCh38 |
NC_000020.10:g.10639045_10639046insGGCTAT , CM000682.1:g.10639045_10639046insGGCTAT | GRCh37 |
NC_000020.9:g.10587045_10587046insGGCTAT | NCBI36 |
NG_007496.1:g.20649_20650insATAGCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.694+70_694+71insATAGCC MANE Select | ENSP00000254958.4:n.694+70_694+71insATAGCC | |
ENST00000254958.9:c.694+70_694+71insATAGCC | ENSP00000254958.4:n.694+70_694+71insATAGCC | |
ENST00000423891.6:n.560+70_560+71insATAGCC | ||
NM_000214.2:c.694+70_694+71insATAGCC | NP_000205.1:n.694+70_694+71insATAGCC | |
NM_000214.3:c.694+70_694+71insATAGCC MANE Select | NP_000205.1:n.694+70_694+71insATAGCC |