HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085155_186085156insT , CM000666.2:g.186085155_186085156insT | GRCh38 |
NC_000004.11:g.187006309_187006310insT , CM000666.1:g.187006309_187006310insT | GRCh37 |
NC_000004.10:g.187243303_187243304insT | NCBI36 |
NG_007278.1:g.21001_21002insT , LRG_117:g.21001_21002insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*2549_*2550insT | ENSP00000513675.1:n.*2549_*2550insT | |
ENST00000698353.1:n.2872_2873insT | ||
ENST00000698354.1:c.*282_*283insT | ENSP00000513676.1:n.*282_*283insT | |
ENST00000296795.8:c.*282_*283insT MANE Select | ENSP00000296795.3:n.*282_*283insT | |
ENST00000296795.7:c.*282_*283insT | ENSP00000296795.2:n.*282_*283insT | |
NM_003265.3:c.*282_*283insT MANE Select | NP_003256.1:n.*282_*283insT |