HGVS | Genome Assembly |
---|---|
NC_000005.10:g.151101039_151101040insT , CM000667.2:g.151101039_151101040insT | GRCh38 |
NC_000005.9:g.150480600_150480601insT , CM000667.1:g.150480600_150480601insT | GRCh37 |
NC_000005.8:g.150460793_150460794insT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000354546.10:c.*408_*409insA MANE Select | ENSP00000346550.5:n.*408_*409insA | |
ENST00000522664.5:c.201-78_201-77insA | ||
NM_001155.4:c.*408_*409insA | NP_001146.2:n.*408_*409insA | |
NM_001193544.1:c.*408_*409insA | NP_001180473.1:n.*408_*409insA | |
NM_001363114.1:c.*408_*409insA | NP_001350043.1:n.*408_*409insA | |
NM_001155.5:c.*408_*409insA MANE Select | NP_001146.2:n.*408_*409insA | |
NM_001193544.2:c.*408_*409insA | NP_001180473.1:n.*408_*409insA | |
NM_001363114.2:c.*408_*409insA | NP_001350043.1:n.*408_*409insA |