HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942308_94942309delinsA , CM000672.2:g.94942308_94942309delinsA | GRCh38 |
NC_000010.10:g.96702065_96702066delinsA , CM000672.1:g.96702065_96702066delinsA | GRCh37 |
NC_000010.9:g.96692055_96692056delinsA | NCBI36 |
NG_008385.1:g.8651_8652delinsA | |
NG_008385.2:g.9151_9152delinsA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.448_449delinsA MANE Select | ENSP00000260682.6:p.Arg150ThrfsTer7 | |
ENST00000643112.1:c.448_449delinsA | ENSP00000496202.1:p.Arg150ThrfsTer7 | |
ENST00000645207.1:n.601_602delinsA | ||
ENST00000260682.6:c.448_449delinsA | ENSP00000260682.6:p.Arg150ThrfsTer7 | |
ENST00000461906.1:n.473_474delinsA | ||
ENST00000473496.1:n.219_220delinsA | ||
NM_000771.3:c.448_449delinsA | NP_000762.2:p.Arg150ThrfsTer7 | |
NM_000771.4:c.448_449delinsA MANE Select | NP_000762.2:p.Arg150ThrfsTer7 |