HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1612805_1612806insCTGTC , CM000668.2:g.1612805_1612806insCTGTC | GRCh38 |
NC_000006.11:g.1613040_1613041insCTGTC , CM000668.1:g.1613040_1613041insCTGTC | GRCh37 |
NC_000006.10:g.1558039_1558040insCTGTC | NCBI36 |
NG_009368.1:g.7360_7361insCTGTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645831.2:c.*698_*699insCTGTC MANE Select | ENSP00000493906.1:n.*698_*699insCTGTC | |
ENST00000380874.3:c.*698_*699insCTGTC | ENSP00000370256.2:n.*698_*699insCTGTC | |
NM_001453.2:c.2360_2361insCTGTC | NP_001444.2:n.2360_2361insCTGTC | |
NM_001453.3:c.*698_*699insCTGTC MANE Select | NP_001444.2:n.*698_*699insCTGTC |