HGVS | Genome Assembly |
---|---|
NC_000017.11:g.34255957_34255958delinsTG , CM000679.2:g.34255957_34255958delinsTG | GRCh38 |
NC_000017.10:g.32582976_32582977delinsTG , CM000679.1:g.32582976_32582977delinsTG | GRCh37 |
NC_000017.9:g.29607089_29607090delinsTG | NCBI36 |
NG_012123.1:g.5681_5682delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000580907.6:c.77-265_77-264delinsTG | ENSP00000462156.1:n.77-265_77-264delinsTG | |
ENST00000624362.2:n.673_674delinsTG | ||
ENST00000225831.4:c.77-265_77-264delinsTG MANE Select | ENSP00000225831.4:n.77-265_77-264delinsTG | |
ENST00000580907.5:c.77-265_77-264delinsTG | ENSP00000462156.1:n.77-265_77-264delinsTG | |
ENST00000624362.1:n.740_741delinsTG | ||
NM_002982.3:c.77-265_77-264delinsTG | NP_002973.1:n.77-265_77-264delinsTG | |
NM_002982.4:c.77-265_77-264delinsTG MANE Select | NP_002973.1:n.77-265_77-264delinsTG |