HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2276601_2276605delinsGGAGA , CM000678.2:g.2276601_2276605delinsGGAGA | GRCh38 |
NC_000016.9:g.2326602_2326606delinsGGAGA , CM000678.1:g.2326602_2326606delinsGGAGA | GRCh37 |
NC_000016.8:g.2266603_2266607delinsGGAGA | NCBI36 |
NG_011790.1:g.69142_69146delinsTCTCC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301732.10:c.*69_*73delinsTCTCC MANE Select | ENSP00000301732.5:n.*69_*73delinsTCTCC | |
ENST00000301732.9:c.*69_*73delinsTCTCC | ENSP00000301732.5:n.*69_*73delinsTCTCC | |
ENST00000382381.7:c.*69_*73delinsTCTCC | ENSP00000371818.3:n.*69_*73delinsTCTCC | |
NM_001089.2:c.*69_*73delinsTCTCC | NP_001080.2:n.*69_*73delinsTCTCC | |
NM_001089.3:c.*69_*73delinsTCTCC MANE Select | NP_001080.2:n.*69_*73delinsTCTCC |