HGVS | Genome Assembly |
---|---|
NC_000012.12:g.120739708_120739709delinsTG , CM000674.2:g.120739708_120739709delinsTG | GRCh38 |
NC_000012.11:g.121177511_121177512delinsTG , CM000674.1:g.121177511_121177512delinsTG | GRCh37 |
NC_000012.10:g.119661894_119661895delinsTG | NCBI36 |
NG_007991.1:g.18941_18942delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242592.9:c.*260_*261delinsTG MANE Select | ENSP00000242592.4:n.*260_*261delinsTG | |
ENST00000242592.8:c.*260_*261delinsTG | ENSP00000242592.4:n.*260_*261delinsTG | |
NM_000017.3:c.*260_*261delinsTG | NP_000008.1:n.*260_*261delinsTG | |
NM_001302554.1:c.*260_*261delinsTG | NP_001289483.1:n.*260_*261delinsTG | |
NM_000017.4:c.*260_*261delinsTG MANE Select | NP_000008.1:n.*260_*261delinsTG | |
NM_001302554.2:c.*260_*261delinsTG | NP_001289483.1:n.*260_*261delinsTG |