HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648405_152648407delinsTTC , CM000669.2:g.152648405_152648407delinsTTC | GRCh38 |
NC_000007.13:g.152345490_152345492delinsTTC , CM000669.1:g.152345490_152345492delinsTTC | GRCh37 |
NC_000007.12:g.151976423_151976425delinsTTC | NCBI36 |
NG_027988.1:g.32759_32761delinsGAA | |
NG_027988.2:g.32759_32761delinsGAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*235_*237delinsGAA | ENSP00000513758.1:n.*235_*237delinsGAA | |
ENST00000359321.2:c.*235_*237delinsGAA MANE Select | ENSP00000352271.1:n.*235_*237delinsGAA | |
ENST00000359321.1:c.*235_*237delinsGAA | ENSP00000352271.1:n.*235_*237delinsGAA | |
ENST00000495707.1:n.1100_1102delinsGAA | ||
NM_005431.1:c.*235_*237delinsGAA | NP_005422.1:n.*235_*237delinsGAA | |
NM_005431.2:c.*235_*237delinsGAA MANE Select | NP_005422.1:n.*235_*237delinsGAA |