HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085481_186085482insGTGGCG , CM000666.2:g.186085481_186085482insGTGGCG | GRCh38 |
NC_000004.11:g.187006635_187006636insGTGGCG , CM000666.1:g.187006635_187006636insGTGGCG | GRCh37 |
NC_000004.10:g.187243629_187243630insGTGGCG | NCBI36 |
NG_007278.1:g.21327_21328insGTGGCG , LRG_117:g.21327_21328insGTGGCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*2875_*2876insGTGGCG | ENSP00000513675.1:n.*2875_*2876insGTGGCG | |
ENST00000698353.1:n.3198_3199insGTGGCG | ||
ENST00000698354.1:c.*608_*609insGTGGCG | ENSP00000513676.1:n.*608_*609insGTGGCG | |
ENST00000296795.8:c.*608_*609insGTGGCG MANE Select | ENSP00000296795.3:n.*608_*609insGTGGCG | |
ENST00000296795.7:c.*608_*609insGTGGCG | ENSP00000296795.2:n.*608_*609insGTGGCG | |
NM_003265.3:c.*608_*609insGTGGCG MANE Select | NP_003256.1:n.*608_*609insGTGGCG |