HGVS | Genome Assembly |
---|---|
NC_000023.11:g.43949854_43949887del , CM000685.2:g.43949854_43949887del | GRCh38 |
NC_000023.10:g.43809100_43809133del , CM000685.1:g.43809100_43809133del | GRCh37 |
NC_000023.9:g.43694044_43694077del | NCBI36 |
NG_009832.1:g.28795_28828del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000642620.1:c.320_353del (NDP) MANE Select | ENSP00000495972.1:p.Arg107ProfsTer? | |
ENST00000647044.1:c.320_353del (NDP) | ENSP00000495811.1:p.Arg107ProfsTer? | |
ENST00000378062.5:c.320_353del (NDP) | ENSP00000367301.5:p.Arg107ProfsTer? | |
ENST00000470584.1:n.364_397del (NDP) | ||
NM_000266.3:c.320_353del (NDP) | NP_000257.1:p.Arg107ProfsTer? | |
NR_046631.1:n.123_156del (NDP-AS1) | ||
NM_000266.4:c.320_353del (NDP) MANE Select | NP_000257.1:p.Arg107ProfsTer? |