HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20188812del , CM000675.2:g.20188812del | GRCh38 |
NC_000013.10:g.20762951del , CM000675.1:g.20762951del | GRCh37 |
NC_000013.9:g.19660951del | NCBI36 |
NG_008358.1:g.9166del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.*91del | ENSP00000372295.1:n.*91del | |
ENST00000382848.5:c.*91del MANE Select | ENSP00000372299.4:n.*91del | |
ENST00000382844.1:c.*91del | ENSP00000372295.1:n.*91del | |
ENST00000382848.4:c.*91del | ENSP00000372299.4:n.*91del | |
NM_004004.5:c.*91del | NP_003995.2:n.*91del | |
XM_011535049.1:c.*91del | XP_011533351.1:n.*91del | |
XM_011535049.2:c.*91del | XP_011533351.1:n.*91del | |
NM_004004.6:c.*91del MANE Select | NP_003995.2:n.*91del |