HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135208_26135209insAAAAA , CM000664.2:g.26135208_26135209insAAAAA | GRCh38 |
NC_000002.11:g.26358077_26358078insAAAAA , CM000664.1:g.26358077_26358078insAAAAA | GRCh37 |
NC_000002.10:g.26211581_26211582insAAAAA | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264710.5:c.*187_*188insAAAAA MANE Select | ENSP00000264710.4:n.*187_*188insAAAAA | |
ENST00000264710.4:c.*187_*188insAAAAA | ENSP00000264710.4:n.*187_*188insAAAAA | |
ENST00000495146.5:n.1153_1154insAAAAA | ||
NM_016131.4:c.*187_*188insAAAAA | NP_057215.3:n.*187_*188insAAAAA | |
XM_024452565.1:c.*187_*188insAAAAA | XP_024308333.1:n.*187_*188insAAAAA | |
NM_016131.5:c.*187_*188insAAAAA MANE Select | NP_057215.3:n.*187_*188insAAAAA |