HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431324_23431326delinsCAG , CM000676.2:g.23431324_23431326delinsCAG | GRCh38 |
NC_000014.8:g.23900533_23900535delinsCAG , CM000676.1:g.23900533_23900535delinsCAG | GRCh37 |
NC_000014.7:g.22970373_22970375delinsCAG | NCBI36 |
NG_007884.1:g.9336_9338delinsCTG , LRG_384:g.9336_9338delinsCTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.796+92_796+94delinsCTG MANE Select | ENSP00000347507.3:n.796+92_796+94delinsCTG | |
ENST00000355349.3:c.796+92_796+94delinsCTG | ENSP00000347507.3:n.796+92_796+94delinsCTG | |
NM_000257.3:c.796+92_796+94delinsCTG | NP_000248.2:n.796+92_796+94delinsCTG | |
XR_245686.3:n.902+92_902+94delinsCTG | ||
XM_017021340.1:c.796+92_796+94delinsCTG | XP_016876829.1:n.796+92_796+94delinsCTG | |
NM_000257.4:c.796+92_796+94delinsCTG MANE Select | NP_000248.2:n.796+92_796+94delinsCTG |