HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648618_152648620delinsCAA , CM000669.2:g.152648618_152648620delinsCAA | GRCh38 |
NC_000007.13:g.152345703_152345705delinsCAA , CM000669.1:g.152345703_152345705delinsCAA | GRCh37 |
NC_000007.12:g.151976636_151976638delinsCAA | NCBI36 |
NG_027988.1:g.32546_32548delinsTTG | |
NG_027988.2:g.32546_32548delinsTTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*22_*24delinsTTG | ENSP00000513758.1:n.*22_*24delinsTTG | |
ENST00000359321.2:c.*22_*24delinsTTG MANE Select | ENSP00000352271.1:n.*22_*24delinsTTG | |
ENST00000359321.1:c.*22_*24delinsTTG | ENSP00000352271.1:n.*22_*24delinsTTG | |
ENST00000495707.1:n.887_889delinsTTG | ||
NM_005431.1:c.*22_*24delinsTTG | NP_005422.1:n.*22_*24delinsTTG | |
NM_005431.2:c.*22_*24delinsTTG MANE Select | NP_005422.1:n.*22_*24delinsTTG |