HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085209_186085210insCTG , CM000666.2:g.186085209_186085210insCTG | GRCh38 |
NC_000004.11:g.187006363_187006364insCTG , CM000666.1:g.187006363_187006364insCTG | GRCh37 |
NC_000004.10:g.187243357_187243358insCTG | NCBI36 |
NG_007278.1:g.21055_21056insCTG , LRG_117:g.21055_21056insCTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*2603_*2604insCTG | ENSP00000513675.1:n.*2603_*2604insCTG | |
ENST00000698353.1:n.2926_2927insCTG | ||
ENST00000698354.1:c.*336_*337insCTG | ENSP00000513676.1:n.*336_*337insCTG | |
ENST00000296795.8:c.*336_*337insCTG MANE Select | ENSP00000296795.3:n.*336_*337insCTG | |
ENST00000296795.7:c.*336_*337insCTG | ENSP00000296795.2:n.*336_*337insCTG | |
NM_003265.3:c.*336_*337insCTG MANE Select | NP_003256.1:n.*336_*337insCTG |