HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190409_204190412delinsTCCC , CM000663.2:g.204190409_204190412delinsTCCC | GRCh38 |
NC_000001.10:g.204159537_204159540delinsTCCC , CM000663.1:g.204159537_204159540delinsTCCC | GRCh37 |
NC_000001.9:g.202426160_202426163delinsTCCC | NCBI36 |
NG_032151.1:g.11080_11083delinsGGGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*72_*75delinsGGGA MANE Select | ENSP00000356162.4:n.*72_*75delinsGGGA | |
ENST00000367194.4:c.*72_*75delinsGGGA | ENSP00000356162.4:n.*72_*75delinsGGGA | |
NM_002256.3:c.*72_*75delinsGGGA | NP_002247.3:n.*72_*75delinsGGGA | |
XM_011509525.1:c.*72_*75delinsGGGA | XP_011507827.1:n.*72_*75delinsGGGA | |
NM_002256.4:c.*72_*75delinsGGGA MANE Select | NP_002247.3:n.*72_*75delinsGGGA |