HGVS | Genome Assembly |
---|---|
NC_000008.11:g.63072906_63072908delinsGAA , CM000670.2:g.63072906_63072908delinsGAA | GRCh38 |
NC_000008.10:g.63985465_63985467delinsGAA , CM000670.1:g.63985465_63985467delinsGAA | GRCh37 |
NC_000008.9:g.64148019_64148021delinsGAA | NCBI36 |
NG_016123.1:g.18146_18148delinsTTC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260116.5:c.358+27_358+29delinsTTC MANE Select | ENSP00000260116.4:n.358+27_358+29delinsTT... | |
ENST00000260116.4:c.358+27_358+29delinsTTC | ENSP00000260116.4:n.358+27_358+29delinsTT... | |
ENST00000521138.1:n.232+12910_232+12912delinsTTC | ||
NM_000370.3:c.358+27_358+29delinsTTC MANE Select | NP_000361.1:n.358+27_358+29delinsTTC | |
XM_006716468.2:c.205-8592_205-8590delinsTTC | XP_006716531.1:n.205-8592_205-8590delinsT... | |
XM_006716468.4:c.205-8592_205-8590delinsTTC | XP_006716531.1:n.205-8592_205-8590delinsT... |