HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42911449_42911450insC , CM000679.2:g.42911449_42911450insC | GRCh38 |
NC_000017.10:g.41063466_41063467insC , CM000679.1:g.41063466_41063467insC | GRCh37 |
NC_000017.9:g.38316992_38316993insC | NCBI36 |
NG_011808.1:g.15652_15653insC , LRG_147:g.15652_15653insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253801.7:c.*23_*24insC MANE Select | ENSP00000253801.1:n.*23_*24insC | |
ENST00000253801.6:c.*23_*24insC | ENSP00000253801.1:n.*23_*24insC | |
ENST00000585489.1:c.*489_*490insC | ENSP00000466202.1:n.*489_*490insC | |
NM_000151.3:c.*23_*24insC | NP_000142.2:n.*23_*24insC | |
NM_001270397.1:c.*489_*490insC | NP_001257326.1:n.*489_*490insC | |
NM_000151.4:c.*23_*24insC MANE Select | NP_000142.2:n.*23_*24insC | |
NM_001270397.2:c.*489_*490insC | NP_001257326.1:n.*489_*490insC |