HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43887179_43887180insAAAAAAAAAA , CM000664.2:g.43887179_43887180insAAAAAAAAAA | GRCh38 |
NC_000002.11:g.44114318_44114319insAAAAAAAAAA , CM000664.1:g.44114318_44114319insAAAAAAAAAA | GRCh37 |
NC_000002.10:g.43967822_43967823insAAAAAAAAAA | NCBI36 |
NG_008247.1:g.113829_113830insTTTTTTTTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2375_2376insTTTTTTTTTT | ||
ENST00000684454.1:n.9472_9473insTTTTTTTTTT | ||
ENST00000260665.12:c.*1423_*1424insTTTTTTTTTT MANE Select | ENSP00000260665.7:n.*1423_*1424insTTTTTTTTTT | |
ENST00000260665.11:c.*1423_*1424insTTTTTTTTTT | ENSP00000260665.7:n.*1423_*1424insTTTTTTTTTT | |
NM_133259.3:c.*1423_*1424insTTTTTTTTTT | NP_573566.2:n.*1423_*1424insTTTTTTTTTT | |
XR_002958896.1:n.5790_5791insTTTTTTTTTT | ||
NM_133259.4:c.*1423_*1424insTTTTTTTTTT MANE Select | NP_573566.2:n.*1423_*1424insTTTTTTTTTT |