HGVS | Genome Assembly |
---|---|
NC_000017.11:g.30211796_30211799del , CM000679.2:g.30211796_30211799del | GRCh38 |
NC_000017.10:g.28538814_28538817del , CM000679.1:g.28538814_28538817del | GRCh37 |
NC_000017.9:g.25562940_25562943del | NCBI36 |
NG_011747.2:g.29140_29143del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650711.1:c.1205-373_1205-370del MANE Select | ENSP00000498537.1:n.1205-373_1205-370del | |
ENST00000261707.7:c.1205-373_1205-370del | ENSP00000261707.3:n.1205-373_1205-370del | |
ENST00000394821.2:c.1205-373_1205-370del | ENSP00000378298.2:n.1205-373_1205-370del | |
ENST00000401766.6:c.1205-373_1205-370del | ENSP00000385822.2:n.1205-373_1205-370del | |
NM_001045.5:c.1205-373_1205-370del | NP_001036.1:n.1205-373_1205-370del | |
NM_001045.6:c.1205-373_1205-370del MANE Select | NP_001036.1:n.1205-373_1205-370del |