HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44249054del , CM000679.2:g.44249054del | GRCh38 |
NC_000017.10:g.42326422del , CM000679.1:g.42326422del | GRCh37 |
NC_000017.9:g.39681948del | NCBI36 |
NG_007498.1:g.24084del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262418.12:c.*1407del MANE Select | ENSP00000262418.6:n.*1407del | |
ENST00000262418.10:c.*1407del | ENSP00000262418.6:n.*1407del | |
ENST00000399246.3:c.*1407del | ENSP00000382190.3:n.*1407del | |
ENST00000631130.1:c.*43del | ENSP00000486787.1:n.*43del | |
NM_000342.3:c.*1407del | NP_000333.1:n.*1407del | |
XM_005257593.3:c.*1407del | XP_005257650.1:n.*1407del | |
XM_011525129.1:c.*1407del | XP_011523431.1:n.*1407del | |
NM_000342.4:c.*1407del MANE Select | NP_000333.1:n.*1407del |