HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135125_26135126insAGAGT , CM000664.2:g.26135125_26135126insAGAGT | GRCh38 |
NC_000002.11:g.26357994_26357995insAGAGT , CM000664.1:g.26357994_26357995insAGAGT | GRCh37 |
NC_000002.10:g.26211498_26211499insAGAGT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*104_*105insAGAGT MANE Select | ENSP00000264710.4:n.*104_*105insAGAGT | |
ENST00000264710.4:c.*104_*105insAGAGT | ENSP00000264710.4:n.*104_*105insAGAGT | |
ENST00000495146.5:n.1070_1071insAGAGT | ||
NM_016131.4:c.*104_*105insAGAGT | NP_057215.3:n.*104_*105insAGAGT | |
XM_024452565.1:c.*104_*105insAGAGT | XP_024308333.1:n.*104_*105insAGAGT | |
NM_016131.5:c.*104_*105insAGAGT MANE Select | NP_057215.3:n.*104_*105insAGAGT |