HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20425747del , CM000684.2:g.20425747del | GRCh38 |
NC_000022.10:g.20780034del , CM000684.1:g.20780034del | GRCh37 |
NC_000022.9:g.19110034del | NCBI36 |
NG_031868.2:g.17113del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622235.5:c.2229del MANE Select | ENSP00000477564.2:p.Arg744GlyfsTer? | |
ENST00000615031.4:c.2244del | ENSP00000479389.1:p.Arg749GlyfsTer? | |
ENST00000622235.4:c.2229del | ENSP00000477564.1:p.Arg744GlyfsTer? | |
ENST00000623402.1:c.2244del | ENSP00000485276.1:p.Arg749GlyfsTer? | |
NM_153334.6:c.2244del | NP_699165.3:p.Arg749GlyfsTer? | |
NM_182895.4:c.2229del | NP_878315.2:p.Arg744GlyfsTer? | |
NM_153334.7:c.2244del | NP_699165.3:p.Arg749GlyfsTer? | |
NM_182895.5:c.2229del MANE Select | NP_878315.2:p.Arg744GlyfsTer? |