HGVS | Genome Assembly |
---|---|
NC_000005.10:g.96392146_96392148delinsCTA , CM000667.2:g.96392146_96392148delinsCTA | GRCh38 |
NC_000005.9:g.95727850_95727852delinsCTA , CM000667.1:g.95727850_95727852delinsCTA | GRCh37 |
NC_000005.8:g.95753606_95753608delinsCTA | NCBI36 |
NG_021161.1:g.46134_46136delinsTAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311106.8:c.*853_*855delinsTAG MANE Select | ENSP00000308024.2:n.*853_*855delinsTAG | |
ENST00000311106.7:c.*853_*855delinsTAG | ENSP00000308024.2:n.*853_*855delinsTAG | |
NM_000439.4:c.*853_*855delinsTAG | NP_000430.3:n.*853_*855delinsTAG | |
NM_001177875.1:c.*853_*855delinsTAG | NP_001171346.1:n.*853_*855delinsTAG | |
NR_130776.1:n.354+12494_354+12496delinsCTA | ||
NM_000439.5:c.*853_*855delinsTAG MANE Select | NP_000430.3:n.*853_*855delinsTAG | |
NM_001177875.2:c.*853_*855delinsTAG | NP_001171346.1:n.*853_*855delinsTAG |