HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204165442_204165450delinsAGGTTAAAT , CM000663.2:g.204165442_204165450delinsAGGTTAAAT | GRCh38 |
NC_000001.10:g.204134570_204134578delinsAGGTTAAAT , CM000663.1:g.204134570_204134578delinsAGGTTAAAT | GRCh37 |
NC_000001.9:g.202401193_202401201delinsAGGTTAAAT | NCBI36 |
NG_012122.1:g.5888_5896delinsATTTAACCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000272190.9:c.98+746_98+754delinsATTTAACCT MANE Select | ENSP00000272190.8:n.98+746_98+754delinsAT... | |
ENST00000638118.1:c.-16-3287_-16-3279delinsATTTAACCT | ENSP00000490307.1:n.-16-3287_-16-3279deli... | |
ENST00000272190.8:c.98+746_98+754delinsATTTAACCT | ENSP00000272190.8:n.98+746_98+754delinsAT... | |
NM_000537.3:c.98+746_98+754delinsATTTAACCT | NP_000528.1:n.98+746_98+754delinsATTTAACC... | |
NM_000537.4:c.98+746_98+754delinsATTTAACCT MANE Select | NP_000528.1:n.98+746_98+754delinsATTTAACC... |