HGVS | Genome Assembly |
---|---|
NC_000023.11:g.43949791_43949794delinsAGCG , CM000685.2:g.43949791_43949794delinsAGCG | GRCh38 |
NC_000023.10:g.43809037_43809040delinsAGCG , CM000685.1:g.43809037_43809040delinsAGCG | GRCh37 |
NC_000023.9:g.43693981_43693984delinsAGCG | NCBI36 |
NG_009832.1:g.28882_28885delinsCGCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000642620.1:c.*5_*8delinsCGCT (NDP) MANE Select | ENSP00000495972.1:n.*5_*8delinsCGCT | |
ENST00000647044.1:c.*5_*8delinsCGCT (NDP) | ENSP00000495811.1:n.*5_*8delinsCGCT | |
ENST00000378062.5:c.*5_*8delinsCGCT (NDP) | ENSP00000367301.5:n.*5_*8delinsCGCT | |
ENST00000470584.1:n.451_454delinsCGCT (NDP) | ||
NM_000266.3:c.*5_*8delinsCGCT (NDP) | NP_000257.1:n.*5_*8delinsCGCT | |
NR_046631.1:n.60_63delinsAGCG (NDP-AS1) | ||
NM_000266.4:c.*5_*8delinsCGCT (NDP) MANE Select | NP_000257.1:n.*5_*8delinsCGCT |