HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186086030_186086031insC , CM000666.2:g.186086030_186086031insC | GRCh38 |
NC_000004.11:g.187007184_187007185insC , CM000666.1:g.187007184_187007185insC | GRCh37 |
NC_000004.10:g.187244178_187244179insC | NCBI36 |
NG_007278.1:g.21876_21877insC , LRG_117:g.21876_21877insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3424_*3425insC | ENSP00000513675.1:n.*3424_*3425insC | |
ENST00000698353.1:n.3747_3748insC | ||
ENST00000698354.1:c.*1157_*1158insC | ENSP00000513676.1:n.*1157_*1158insC | |
ENST00000296795.8:c.*1157_*1158insC MANE Select | ENSP00000296795.3:n.*1157_*1158insC | |
ENST00000296795.7:c.*1157_*1158insC | ENSP00000296795.2:n.*1157_*1158insC | |
NM_003265.3:c.*1157_*1158insC MANE Select | NP_003256.1:n.*1157_*1158insC |