HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734125_4734126delinsGA , CM000679.2:g.4734125_4734126delinsGA | GRCh38 |
NC_000017.10:g.4637420_4637421delinsGA , CM000679.1:g.4637420_4637421delinsGA | GRCh37 |
NC_000017.9:g.4584169_4584170delinsGA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*377_*378delinsTC MANE Select | ENSP00000293778.7:n.*377_*378delinsTC | |
ENST00000293778.10:c.*377_*378delinsTC | ENSP00000293778.6:n.*377_*378delinsTC | |
ENST00000576153.5:n.933_934delinsTC | ||
NM_022059.3:c.*377_*378delinsTC | NP_071342.2:n.*377_*378delinsTC | |
NM_022059.4:c.*377_*378delinsTC | NP_071342.2:n.*377_*378delinsTC | |
NM_001386809.1:c.*377_*378delinsTC MANE Select | NP_001373738.1:n.*377_*378delinsTC |