HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648406_152648407delinsTC , CM000669.2:g.152648406_152648407delinsTC | GRCh38 |
NC_000007.13:g.152345491_152345492delinsTC , CM000669.1:g.152345491_152345492delinsTC | GRCh37 |
NC_000007.12:g.151976424_151976425delinsTC | NCBI36 |
NG_027988.1:g.32759_32760delinsGA | |
NG_027988.2:g.32759_32760delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*235_*236delinsGA | ENSP00000513758.1:n.*235_*236delinsGA | |
ENST00000359321.2:c.*235_*236delinsGA MANE Select | ENSP00000352271.1:n.*235_*236delinsGA | |
ENST00000359321.1:c.*235_*236delinsGA | ENSP00000352271.1:n.*235_*236delinsGA | |
ENST00000495707.1:n.1100_1101delinsGA | ||
NM_005431.1:c.*235_*236delinsGA | NP_005422.1:n.*235_*236delinsGA | |
NM_005431.2:c.*235_*236delinsGA MANE Select | NP_005422.1:n.*235_*236delinsGA |