HGVS | Genome Assembly |
---|---|
NC_000023.11:g.43949968_43950010del , CM000685.2:g.43949968_43950010del | GRCh38 |
NC_000023.10:g.43809214_43809256del , CM000685.1:g.43809214_43809256del | GRCh37 |
NC_000023.9:g.43694158_43694200del | NCBI36 |
NG_009832.1:g.28670_28712del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000642620.1:c.195_237del (NDP) MANE Select | ENSP00000495972.1:p.Glu66ArgfsTer24 | |
ENST00000647044.1:c.195_237del (NDP) | ENSP00000495811.1:p.Glu66ArgfsTer24 | |
ENST00000378062.5:c.195_237del (NDP) | ENSP00000367301.5:p.Glu66ArgfsTer24 | |
ENST00000470584.1:n.239_281del (NDP) | ||
NM_000266.3:c.195_237del (NDP) | NP_000257.1:p.Glu66ArgfsTer24 | |
NR_046631.1:n.237_279del (NDP-AS1) | ||
NM_000266.4:c.195_237del (NDP) MANE Select | NP_000257.1:p.Glu66ArgfsTer24 |