HGVS | Genome Assembly |
---|---|
NC_000004.12:g.87612011_87612029delinsTTGTGTGTGTGTGTGTGTG , CM000666.2:g.87612011_87612029delinsTTGTGTGTGTGTGTGTGTG | GRCh38 |
NC_000004.11:g.88533163_88533181delinsTTGTGTGTGTGTGTGTGTG , CM000666.1:g.88533163_88533181delinsTTGTGTGTGTGTGTGTGTG | GRCh37 |
NC_000004.10:g.88752187_88752205delinsTTGTGTGTGTGTGTGTGTG | NCBI36 |
NG_011595.1:g.8483_8501delinsTTGTGTGTGTGTGTGTGTG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651931.1:c.52-94_52-76delinsTTGTGTGTGTGTGTGTGTG MANE Select | ENSP00000498766.1:n.52-94_52-76delinsTTGT... | |
ENST00000282478.7:c.52-94_52-76delinsTTGTGTGTGTGTGTGTGTG | ENSP00000282478.7:n.52-94_52-76delinsTTGT... | |
ENST00000399271.5:c.52-94_52-76delinsTTGTGTGTGTGTGTGTGTG | ENSP00000382213.1:n.52-94_52-76delinsTTGT... | |
NM_014208.3:c.52-94_52-76delinsTTGTGTGTGTGTGTGTGTG MANE Select | NP_055023.2:n.52-94_52-76delinsTTGTGTGTGT... |