HGVS | Genome Assembly |
---|---|
NC_000005.10:g.151101043_151101077del , CM000667.2:g.151101043_151101077del | GRCh38 |
NC_000005.9:g.150480604_150480638del , CM000667.1:g.150480604_150480638del | GRCh37 |
NC_000005.8:g.150460797_150460831del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000354546.10:c.*374_*408del MANE Select | ENSP00000346550.5:n.*374_*408del | |
ENST00000522664.5:c.201-112_201-78del | ||
NM_001155.4:c.*374_*408del | NP_001146.2:n.*374_*408del | |
NM_001193544.1:c.*374_*408del | NP_001180473.1:n.*374_*408del | |
NM_001363114.1:c.*374_*408del | NP_001350043.1:n.*374_*408del | |
NM_001155.5:c.*374_*408del MANE Select | NP_001146.2:n.*374_*408del | |
NM_001193544.2:c.*374_*408del | NP_001180473.1:n.*374_*408del | |
NM_001363114.2:c.*374_*408del | NP_001350043.1:n.*374_*408del |