HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40843712_40843713insTACCC , CM000681.2:g.40843712_40843713insTACCC | GRCh38 |
NC_000019.9:g.41349617_41349618insTACCC , CM000681.1:g.41349617_41349618insTACCC | GRCh37 |
NC_000019.8:g.46041457_46041458insTACCC | NCBI36 |
NG_008377.1:g.11735_11736insGGGTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301141.10:c.*83_*84insGGGTA MANE Select | ENSP00000301141.4:n.*83_*84insGGGTA | |
ENST00000301141.9:c.*83_*84insGGGTA | ENSP00000301141.4:n.*83_*84insGGGTA | |
ENST00000599960.1:n.487_488insGGGTA | ||
ENST00000601627.1:c.119+42297_119+42298insTACCC | ||
NM_000762.5:c.*83_*84insGGGTA | NP_000753.3:n.*83_*84insGGGTA | |
NM_000762.6:c.*83_*84insGGGTA MANE Select | NP_000753.3:n.*83_*84insGGGTA |