HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94989076_94989077insA , CM000672.2:g.94989076_94989077insA | GRCh38 |
NC_000010.10:g.96748833_96748834insA , CM000672.1:g.96748833_96748834insA | GRCh37 |
NC_000010.9:g.96738823_96738824insA | NCBI36 |
NG_008385.1:g.55419_55420insA | |
NG_008385.2:g.55919_55920insA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.*48_*49insA MANE Select | ENSP00000260682.6:n.*48_*49insA | |
ENST00000643112.1:c.*530_*531insA | ENSP00000496202.1:n.*530_*531insA | |
ENST00000260682.6:c.*48_*49insA | ENSP00000260682.6:n.*48_*49insA | |
NM_000771.3:c.*48_*49insA | NP_000762.2:n.*48_*49insA | |
NM_000771.4:c.*48_*49insA MANE Select | NP_000762.2:n.*48_*49insA |