HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2276587_2276588delinsGA , CM000678.2:g.2276587_2276588delinsGA | GRCh38 |
NC_000016.9:g.2326588_2326589delinsGA , CM000678.1:g.2326588_2326589delinsGA | GRCh37 |
NC_000016.8:g.2266589_2266590delinsGA | NCBI36 |
NG_011790.1:g.69159_69160delinsTC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301732.10:c.*86_*87delinsTC MANE Select | ENSP00000301732.5:n.*86_*87delinsTC | |
ENST00000301732.9:c.*86_*87delinsTC | ENSP00000301732.5:n.*86_*87delinsTC | |
ENST00000382381.7:c.*86_*87delinsTC | ENSP00000371818.3:n.*86_*87delinsTC | |
NM_001089.2:c.*86_*87delinsTC | NP_001080.2:n.*86_*87delinsTC | |
NM_001089.3:c.*86_*87delinsTC MANE Select | NP_001080.2:n.*86_*87delinsTC |