HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55091579_55091580insGAAG , CM000666.2:g.55091579_55091580insGAAG | GRCh38 |
NC_000004.11:g.55957746_55957747insGAAG , CM000666.1:g.55957746_55957747insGAAG | GRCh37 |
NC_000004.10:g.55652503_55652504insGAAG | NCBI36 |
NG_012004.1:g.39016_39017insCTTC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263923.5:c.3069+1037_3069+1038insCTTC MANE Select | ENSP00000263923.4:n.3069+1037_3069+1038in... | |
ENST00000647068.1:n.3082+1037_3082+1038insCTTC | ||
ENST00000263923.4:c.3069+1037_3069+1038insCTTC | ENSP00000263923.4:n.3069+1037_3069+1038in... | |
NM_002253.2:c.3069+1037_3069+1038insCTTC | NP_002244.1:n.3069+1037_3069+1038insCTTC | |
NM_002253.3:c.3069+1037_3069+1038insCTTC | NP_002244.1:n.3069+1037_3069+1038insCTTC | |
NM_002253.4:c.3069+1037_3069+1038insCTTC MANE Select | NP_002244.1:n.3069+1037_3069+1038insCTTC |