HGVS | Genome Assembly |
---|---|
NC_000008.11:g.81478705_81478706delinsAG , CM000670.2:g.81478705_81478706delinsAG | GRCh38 |
NC_000008.10:g.82390940_82390941delinsAG , CM000670.1:g.82390940_82390941delinsAG | GRCh37 |
NC_000008.9:g.82553495_82553496delinsAG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256104.5:c.*159_*160delinsCT MANE Select | ENSP00000256104.4:n.*159_*160delinsCT | |
ENST00000256104.4:c.*159_*160delinsCT | ENSP00000256104.4:n.*159_*160delinsCT | |
ENST00000518669.5:n.493_494delinsCT | ||
ENST00000522659.1:c.*434_*435delinsCT | ENSP00000428385.1:n.*434_*435delinsCT | |
NM_001442.2:c.*159_*160delinsCT | NP_001433.1:n.*159_*160delinsCT | |
XR_001745980.1:n.514+16731_514+16732delinsAG | ||
NM_001442.3:c.*159_*160delinsCT MANE Select | NP_001433.1:n.*159_*160delinsCT |