HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43887179_43887180insAAAAAAAAA , CM000664.2:g.43887179_43887180insAAAAAAAAA | GRCh38 |
NC_000002.11:g.44114318_44114319insAAAAAAAAA , CM000664.1:g.44114318_44114319insAAAAAAAAA | GRCh37 |
NC_000002.10:g.43967822_43967823insAAAAAAAAA | NCBI36 |
NG_008247.1:g.113829_113830insTTTTTTTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2375_2376insTTTTTTTTT | ||
ENST00000684454.1:n.9472_9473insTTTTTTTTT | ||
ENST00000260665.12:c.*1423_*1424insTTTTTTTTT MANE Select | ENSP00000260665.7:n.*1423_*1424insTTTTTTTTT | |
ENST00000260665.11:c.*1423_*1424insTTTTTTTTT | ENSP00000260665.7:n.*1423_*1424insTTTTTTTTT | |
NM_133259.3:c.*1423_*1424insTTTTTTTTT | NP_573566.2:n.*1423_*1424insTTTTTTTTT | |
XR_002958896.1:n.5790_5791insTTTTTTTTT | ||
NM_133259.4:c.*1423_*1424insTTTTTTTTT MANE Select | NP_573566.2:n.*1423_*1424insTTTTTTTTT |