HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136648180_136648184delinsTTGAC , CM000685.2:g.136648180_136648184delinsTTGAC | GRCh38 |
NC_000023.10:g.135730339_135730343delinsTTGAC , CM000685.1:g.135730339_135730343delinsTTGAC | GRCh37 |
NC_000023.9:g.135558005_135558009delinsTTGAC | NCBI36 |
NG_007280.1:g.5004_5008delinsTTGAC , LRG_141:g.5004_5008delinsTTGAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000695724.1:c.-69_-65delinsTTGAC | ENSP00000512122.1:n.-69_-65delinsTTGAC | |
ENST00000695725.1:c.-69_-65delinsTTGAC | ENSP00000512123.1:n.-69_-65delinsTTGAC | |
ENST00000370629.7:c.-69_-65delinsTTGAC MANE Select | ENSP00000359663.2:n.-69_-65delinsTTGAC | |
NM_000074.2:c.-69_-65delinsTTGAC , LRG_141t1:c.-69_-65delinsTTGAC | NP_000065.1:n.-69_-65delinsTTGAC | |
NM_000074.3:c.-69_-65delinsTTGAC MANE Select | NP_000065.1:n.-69_-65delinsTTGAC |