HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102527861_102527862delinsT , CM000673.2:g.102527861_102527862delinsT | GRCh38 |
NC_000011.9:g.102398592_102398593delinsT , CM000673.1:g.102398592_102398593delinsT | GRCh37 |
NC_000011.8:g.101903802_101903803delinsT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260227.5:c.230_231delinsA MANE Select | ENSP00000260227.4:p.Arg77GlnfsTer3 | |
ENST00000260227.4:c.230_231delinsA | ENSP00000260227.4:p.Arg77GlnfsTer3 | |
ENST00000531200.1:n.277_278delinsA | ||
ENST00000533366.5:n.280_281delinsA | ||
NM_002423.3:c.230_231delinsA | NP_002414.1:p.Arg77GlnfsTer3 | |
NM_002423.4:c.230_231delinsA | NP_002414.1:p.Arg77GlnfsTer3 | |
NM_002423.5:c.230_231delinsA MANE Select | NP_002414.1:p.Arg77GlnfsTer3 |