HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6319104_6319112delinsCTGAAAGGA , CM000673.2:g.6319104_6319112delinsCTGAAAGGA | GRCh38 |
NC_000011.9:g.6340334_6340342delinsCTGAAAGGA , CM000673.1:g.6340334_6340342delinsCTGAAAGGA | GRCh37 |
NC_000011.8:g.6296910_6296918delinsCTGAAAGGA | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000303927.4:c.*51_*59delinsTCCTTTCAG MANE Select | ENSP00000307292.3:n.*51_*59delinsTCCTTTCA... | |
ENST00000303927.3:c.*51_*59delinsTCCTTTCAG | ENSP00000307292.3:n.*51_*59delinsTCCTTTCA... | |
ENST00000532354.1:n.859_867delinsTCCTTTCAG | ||
NM_145040.2:c.*51_*59delinsTCCTTTCAG | NP_659477.2:n.*51_*59delinsTCCTTTCAG | |
XR_930997.1:n.720+884_720+892delinsCTGAAAGGA | ||
NM_145040.3:c.*51_*59delinsTCCTTTCAG MANE Select | NP_659477.2:n.*51_*59delinsTCCTTTCAG |