HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085796_186085797delinsAT , CM000666.2:g.186085796_186085797delinsAT | GRCh38 |
NC_000004.11:g.187006950_187006951delinsAT , CM000666.1:g.187006950_187006951delinsAT | GRCh37 |
NC_000004.10:g.187243944_187243945delinsAT | NCBI36 |
NG_007278.1:g.21642_21643delinsAT , LRG_117:g.21642_21643delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3190_*3191delinsAT | ENSP00000513675.1:n.*3190_*3191delinsAT | |
ENST00000698353.1:n.3513_3514delinsAT | ||
ENST00000698354.1:c.*923_*924delinsAT | ENSP00000513676.1:n.*923_*924delinsAT | |
ENST00000296795.8:c.*923_*924delinsAT MANE Select | ENSP00000296795.3:n.*923_*924delinsAT | |
ENST00000296795.7:c.*923_*924delinsAT | ENSP00000296795.2:n.*923_*924delinsAT | |
NM_003265.3:c.*923_*924delinsAT MANE Select | NP_003256.1:n.*923_*924delinsAT |