HGVS | Genome Assembly |
---|---|
NC_000006.12:g.111222909_111222910insT , CM000668.2:g.111222909_111222910insT | GRCh38 |
NC_000006.11:g.111544112_111544113insT , CM000668.1:g.111544112_111544113insT | GRCh37 |
NC_000006.10:g.111650805_111650806insT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368851.10:c.*674_*675insT MANE Select | ENSP00000357844.4:n.*674_*675insT | |
ENST00000368850.4:c.*674_*675insT | ENSP00000357843.1:n.*674_*675insT | |
ENST00000368851.9:c.*674_*675insT | ENSP00000357844.4:n.*674_*675insT | |
NM_018593.4:c.*674_*675insT | NP_061063.2:n.*674_*675insT | |
XM_005266818.2:c.*628_*629insT | XP_005266875.1:n.*628_*629insT | |
XM_017010237.1:c.*674_*675insT | XP_016865726.1:n.*674_*675insT | |
XR_001743158.1:n.2504_2505insT | ||
NM_018593.5:c.*674_*675insT MANE Select | NP_061063.2:n.*674_*675insT |