HGVS | Genome Assembly |
---|---|
NC_000022.11:g.29313222_29313224del , CM000684.2:g.29313222_29313224del | GRCh38 |
NC_000022.10:g.29709211_29709213del , CM000684.1:g.29709211_29709213del | GRCh37 |
NC_000022.9:g.28039211_28039213del | NCBI36 |
NG_032959.1:g.11216_11218del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216101.7:c.*78_*80del MANE Select | ENSP00000216101.6:n.*78_*80del | |
ENST00000216101.6:c.*78_*80del | ENSP00000216101.6:n.*78_*80del | |
ENST00000401450.3:c.*636_*638del | ENSP00000386095.3:n.*636_*638del | |
NM_006477.4:c.*78_*80del | NP_006468.1:n.*78_*80del | |
XM_011529821.1:c.*78_*80del | XP_011528123.1:n.*78_*80del | |
XM_011529822.1:c.*78_*80del | XP_011528124.1:n.*78_*80del | |
XM_011529823.1:c.*78_*80del | XP_011528125.1:n.*78_*80del | |
NM_006477.5:c.*78_*80del MANE Select | NP_006468.1:n.*78_*80del |