HGVS | Genome Assembly |
---|---|
NC_000023.11:g.108084523_108084524delinsCG , CM000685.2:g.108084523_108084524delinsCG | GRCh38 |
NC_000023.10:g.107327753_107327754delinsCG , CM000685.1:g.107327753_107327754delinsCG | GRCh37 |
NC_000023.9:g.107214409_107214410delinsCG | NCBI36 |
NG_012521.1:g.12095_12096delinsCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217958.8:c.*450_*451delinsCG MANE Select | ENSP00000217958.3:n.*450_*451delinsCG | |
ENST00000217958.7:c.*450_*451delinsCG | ENSP00000217958.3:n.*450_*451delinsCG | |
NM_002814.3:c.*450_*451delinsCG | NP_002805.1:n.*450_*451delinsCG | |
NM_170750.2:c.*596_*597delinsCG | NP_736606.1:n.*596_*597delinsCG | |
NM_002814.4:c.*450_*451delinsCG MANE Select | NP_002805.1:n.*450_*451delinsCG | |
NM_170750.3:c.*596_*597delinsCG | NP_736606.1:n.*596_*597delinsCG |