HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431324_23431328delinsCAGAG , CM000676.2:g.23431324_23431328delinsCAGAG | GRCh38 |
NC_000014.8:g.23900533_23900537delinsCAGAG , CM000676.1:g.23900533_23900537delinsCAGAG | GRCh37 |
NC_000014.7:g.22970373_22970377delinsCAGAG | NCBI36 |
NG_007884.1:g.9334_9338delinsCTCTG , LRG_384:g.9334_9338delinsCTCTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.796+90_796+94delinsCTCTG MANE Select | ENSP00000347507.3:n.796+90_796+94delinsCTCTG | |
ENST00000355349.3:c.796+90_796+94delinsCTCTG | ENSP00000347507.3:n.796+90_796+94delinsCTCTG | |
NM_000257.3:c.796+90_796+94delinsCTCTG | NP_000248.2:n.796+90_796+94delinsCTCTG | |
XR_245686.3:n.902+90_902+94delinsCTCTG | ||
XM_017021340.1:c.796+90_796+94delinsCTCTG | XP_016876829.1:n.796+90_796+94delinsCTCTG | |
NM_000257.4:c.796+90_796+94delinsCTCTG MANE Select | NP_000248.2:n.796+90_796+94delinsCTCTG |