HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20188866del , CM000675.2:g.20188866del | GRCh38 |
NC_000013.10:g.20763005del , CM000675.1:g.20763005del | GRCh37 |
NC_000013.9:g.19661005del | NCBI36 |
NG_008358.1:g.9110del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.*35del | ENSP00000372295.1:n.*35del | |
ENST00000382848.5:c.*35del MANE Select | ENSP00000372299.4:n.*35del | |
ENST00000382844.1:c.*35del | ENSP00000372295.1:n.*35del | |
ENST00000382848.4:c.*35del | ENSP00000372299.4:n.*35del | |
NM_004004.5:c.*35del | NP_003995.2:n.*35del | |
XM_011535049.1:c.*35del | XP_011533351.1:n.*35del | |
XM_011535049.2:c.*35del | XP_011533351.1:n.*35del | |
NM_004004.6:c.*35del MANE Select | NP_003995.2:n.*35del |