HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6318991_6318992insTCTCG , CM000673.2:g.6318991_6318992insTCTCG | GRCh38 |
NC_000011.9:g.6340221_6340222insTCTCG , CM000673.1:g.6340221_6340222insTCTCG | GRCh37 |
NC_000011.8:g.6296797_6296798insTCTCG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303927.4:c.*171_*172insCGAGA MANE Select | ENSP00000307292.3:n.*171_*172insCGAGA | |
ENST00000303927.3:c.*171_*172insCGAGA | ENSP00000307292.3:n.*171_*172insCGAGA | |
ENST00000532354.1:n.979_980insCGAGA | ||
NM_145040.2:c.*171_*172insCGAGA | NP_659477.2:n.*171_*172insCGAGA | |
XR_930997.1:n.720+771_720+772insTCTCG | ||
NM_145040.3:c.*171_*172insCGAGA MANE Select | NP_659477.2:n.*171_*172insCGAGA |