HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52033587_52033592delinsTCTCTC , CM000666.2:g.52033587_52033592delinsTCTCTC | GRCh38 |
NC_000004.11:g.52899753_52899758delinsTCTCTC , CM000666.1:g.52899753_52899758delinsTCTCTC | GRCh37 |
NC_000004.10:g.52594510_52594515delinsTCTCTC | NCBI36 |
NG_008891.1:g.9728_9733delinsGAGAGA , LRG_204:g.9728_9733delinsGAGAGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.82_87delinsGAGAGA MANE Select | ENSP00000370839.6:p.Glu28= | |
ENST00000381431.9:c.82_87delinsGAGAGA | ENSP00000370839.5:p.Glu28= | |
ENST00000506357.5:c.68_73delinsGAGAGA | ||
ENST00000514133.1:c.49_54delinsGAGAGA | ENSP00000425818.1:p.Glu17= | |
NM_000232.4:c.82_87delinsGAGAGA , LRG_204t1:c.82_87delinsGAGAGA | NP_000223.1:p.Glu28= | |
XM_011534403.1:c.34-3729_34-3724delinsGAGAGA | XP_011532705.1:n.34-3729_34-3724delinsGAGAGA | |
NM_000232.5:c.82_87delinsGAGAGA MANE Select | NP_000223.1:p.Glu28= |