HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431164_23431167delinsCAGA , CM000676.2:g.23431164_23431167delinsCAGA | GRCh38 |
NC_000014.8:g.23900373_23900376delinsCAGA , CM000676.1:g.23900373_23900376delinsCAGA | GRCh37 |
NC_000014.7:g.22970213_22970216delinsCAGA | NCBI36 |
NG_007884.1:g.9495_9498delinsTCTG , LRG_384:g.9495_9498delinsTCTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.797-168_797-165delinsTCTG MANE Select | ENSP00000347507.3:n.797-168_797-165delinsTCTG | |
ENST00000355349.3:c.797-168_797-165delinsTCTG | ENSP00000347507.3:n.797-168_797-165delinsTCTG | |
NM_000257.3:c.797-168_797-165delinsTCTG | NP_000248.2:n.797-168_797-165delinsTCTG | |
XR_245686.3:n.903-168_903-165delinsTCTG | ||
XM_017021340.1:c.797-168_797-165delinsTCTG | XP_016876829.1:n.797-168_797-165delinsTCTG | |
NM_000257.4:c.797-168_797-165delinsTCTG MANE Select | NP_000248.2:n.797-168_797-165delinsTCTG |