HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315926_159315927insAAAAC , CM000667.2:g.159315926_159315927insAAAAC | GRCh38 |
NC_000005.9:g.158742934_158742935insAAAAC , CM000667.1:g.158742934_158742935insAAAAC | GRCh37 |
NC_000005.8:g.158675512_158675513insAAAAC | NCBI36 |
NG_009618.1:g.19547_19548insGTTTT , LRG_71:g.19547_19548insGTTTT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*174_*175insGTTTT | ENSP00000512849.1:n.*174_*175insGTTTT | |
ENST00000696751.1:c.*656_*657insGTTTT | ENSP00000512850.1:n.*656_*657insGTTTT | |
ENST00000231228.3:c.*174_*175insGTTTT MANE Select | ENSP00000231228.2:n.*174_*175insGTTTT | |
ENST00000231228.2:c.*174_*175insGTTTT | ENSP00000231228.2:n.*174_*175insGTTTT | |
NM_002187.2:c.*174_*175insGTTTT , LRG_71t1:c.*174_*175insGTTTT | NP_002178.2:n.*174_*175insGTTTT | |
NM_002187.3:c.*174_*175insGTTTT MANE Select | NP_002178.2:n.*174_*175insGTTTT |