HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159316007_159316008delinsAG , CM000667.2:g.159316007_159316008delinsAG | GRCh38 |
NC_000005.9:g.158743015_158743016delinsAG , CM000667.1:g.158743015_158743016delinsAG | GRCh37 |
NC_000005.8:g.158675593_158675594delinsAG | NCBI36 |
NG_009618.1:g.19466_19467delinsCT , LRG_71:g.19466_19467delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*93_*94delinsCT | ENSP00000512849.1:n.*93_*94delinsCT | |
ENST00000696751.1:c.*575_*576delinsCT | ENSP00000512850.1:n.*575_*576delinsCT | |
ENST00000231228.3:c.*93_*94delinsCT MANE Select | ENSP00000231228.2:n.*93_*94delinsCT | |
ENST00000231228.2:c.*93_*94delinsCT | ENSP00000231228.2:n.*93_*94delinsCT | |
NM_002187.2:c.*93_*94delinsCT , LRG_71t1:c.*93_*94delinsCT | NP_002178.2:n.*93_*94delinsCT | |
NM_002187.3:c.*93_*94delinsCT MANE Select | NP_002178.2:n.*93_*94delinsCT |