HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55039902_55039903insGCA , CM000663.2:g.55039902_55039903insGCA | GRCh38 |
NC_000001.10:g.55505575_55505576insGCA , CM000663.1:g.55505575_55505576insGCA | GRCh37 |
NC_000001.9:g.55278163_55278164insGCA | NCBI36 |
NG_009061.1:g.5356_5357insGCA , LRG_275:g.5356_5357insGCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.65_66insGCA | ENSP00000501161.2:p.Leu22_Leu23insHis | |
ENST00000710286.1:c.422_423insGCA | ENSP00000518176.1:p.Leu141_Leu142insHis | |
ENST00000673726.1:c.65_66insGCA | ENSP00000501004.1:p.Leu22_Leu23insHis | |
ENST00000302118.5:c.65_66insGCA MANE Select | ENSP00000303208.5:p.Leu22_Leu23insHis | |
NM_174936.3:c.65_66insGCA , LRG_275t1:c.65_66insGCA | NP_777596.2:p.Leu22_Leu23insHis | |
NM_174936.4:c.65_66insGCA MANE Select | NP_777596.2:p.Leu22_Leu23insHis |