HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133539044_133539048delinsCCTTT , CM000672.2:g.133539044_133539048delinsCCTTT | GRCh38 |
NC_000010.10:g.135352548_135352552delinsCCTTT , CM000672.1:g.135352548_135352552delinsCCTTT | GRCh37 |
NC_000010.9:g.135202538_135202542delinsCCTTT | NCBI36 |
NG_008383.1:g.16682_16686delinsCCTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252945.8:c.*80_*84delinsCCTTT MANE Select | ENSP00000252945.3:n.*80_*84delinsCCTTT | |
ENST00000252945.7:c.*80_*84delinsCCTTT | ENSP00000252945.3:n.*80_*84delinsCCTTT | |
ENST00000368520.1:n.1358+1152_1358+1156delinsCCTTT | ||
ENST00000463117.6:c.*80_*84delinsCCTTT | ENSP00000440689.1:n.*80_*84delinsCCTTT | |
ENST00000469258.1:n.658_662delinsCCTTT | ||
NM_000773.3:c.*80_*84delinsCCTTT | NP_000764.1:n.*80_*84delinsCCTTT | |
NM_000773.4:c.*80_*84delinsCCTTT MANE Select | NP_000764.1:n.*80_*84delinsCCTTT |