HGVS | Genome Assembly |
---|---|
NC_000005.10:g.175441537_175441538insATAA , CM000667.2:g.175441537_175441538insATAA | GRCh38 |
NC_000005.9:g.174868540_174868541insATAA , CM000667.1:g.174868540_174868541insATAA | GRCh37 |
NC_000005.8:g.174801146_174801147insATAA | NCBI36 |
NG_011802.1:g.7623_7624insTTAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393752.3:c.*221_*222insTTAT MANE Select | ENSP00000377353.1:n.*221_*222insTTAT | |
ENST00000393752.2:c.*221_*222insTTAT | ENSP00000377353.1:n.*221_*222insTTAT | |
NM_000794.3:c.*221_*222insTTAT | NP_000785.1:n.*221_*222insTTAT | |
NM_000794.4:c.*221_*222insTTAT | NP_000785.1:n.*221_*222insTTAT | |
NM_000794.5:c.*221_*222insTTAT MANE Select | NP_000785.1:n.*221_*222insTTAT |