HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085739_186085742delinsGTGA , CM000666.2:g.186085739_186085742delinsGTGA | GRCh38 |
NC_000004.11:g.187006893_187006896delinsGTGA , CM000666.1:g.187006893_187006896delinsGTGA | GRCh37 |
NC_000004.10:g.187243887_187243890delinsGTGA | NCBI36 |
NG_007278.1:g.21585_21588delinsGTGA , LRG_117:g.21585_21588delinsGTGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3133_*3136delinsGTGA | ENSP00000513675.1:n.*3133_*3136delinsGTGA | |
ENST00000698353.1:n.3456_3459delinsGTGA | ||
ENST00000698354.1:c.*866_*869delinsGTGA | ENSP00000513676.1:n.*866_*869delinsGTGA | |
ENST00000296795.8:c.*866_*869delinsGTGA MANE Select | ENSP00000296795.3:n.*866_*869delinsGTGA | |
ENST00000296795.7:c.*866_*869delinsGTGA | ENSP00000296795.2:n.*866_*869delinsGTGA | |
NM_003265.3:c.*866_*869delinsGTGA MANE Select | NP_003256.1:n.*866_*869delinsGTGA |