HGVS | Genome Assembly |
---|---|
NC_000015.10:g.90501243_90501253del , CM000677.2:g.90501243_90501253del | GRCh38 |
NC_000015.9:g.91044475_91044485del , CM000677.1:g.91044475_91044485del | GRCh37 |
NC_000015.8:g.88845479_88845489del | NCBI36 |
NG_052946.1:g.118003_118013del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000268182.10:c.*1135_*1145del MANE Select | ENSP00000268182.5:n.*1135_*1145del | |
ENST00000268182.9:c.*1135_*1145del | ENSP00000268182.5:n.*1135_*1145del | |
ENST00000558957.1:n.2167_2177del | ||
ENST00000561086.1:n.1876_1886del | ||
NM_003870.3:c.*1135_*1145del | NP_003861.1:n.*1135_*1145del | |
XR_001751409.2:n.6238_6248del | ||
NM_003870.4:c.*1135_*1145del MANE Select | NP_003861.1:n.*1135_*1145del |