HGVS | Genome Assembly |
---|---|
NC_000022.11:g.27750851_27750852delinsAG , CM000684.2:g.27750851_27750852delinsAG | GRCh38 |
NC_000022.10:g.28146839_28146840delinsAG , CM000684.1:g.28146839_28146840delinsAG | GRCh37 |
NC_000022.9:g.26476839_26476840delinsAG | NCBI36 |
NG_023258.1:g.55647_55648delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000703102.1:n.551_552delinsCT | ||
ENST00000302326.5:c.*63_*64delinsCT MANE Select | ENSP00000304956.4:n.*63_*64delinsCT | |
ENST00000302326.4:c.*63_*64delinsCT | ENSP00000304956.4:n.*63_*64delinsCT | |
ENST00000424656.1:c.379_380delinsCT | ||
ENST00000497225.1:n.382_383delinsCT | ||
NM_002430.2:c.*63_*64delinsCT | NP_002421.3:n.*63_*64delinsCT | |
NM_002430.3:c.*63_*64delinsCT MANE Select | NP_002421.3:n.*63_*64delinsCT |