HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190483_204190484delinsCT , CM000663.2:g.204190483_204190484delinsCT | GRCh38 |
NC_000001.10:g.204159611_204159612delinsCT , CM000663.1:g.204159611_204159612delinsCT | GRCh37 |
NC_000001.9:g.202426234_202426235delinsCT | NCBI36 |
NG_032151.1:g.11008_11009delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.417_*1delinsAG MANE Select | ENSP00000356162.4:n.[c.417_*1delinsAG;Ter139=] | |
ENST00000367194.4:c.417_*1delinsAG | ENSP00000356162.4:n.[c.417_*1delinsAG;Ter139=] | |
ENST00000625357.1:c.415-2_415-1delinsAG | ENSP00000485957.1:n.415-2_415-1delinsAG | |
NM_002256.3:c.417_*1delinsAG | NP_002247.3:n.[c.417_*1delinsAG;Ter139=] | |
XM_011509525.1:c.417_*1delinsAG | XP_011507827.1:n.[c.417_*1delinsAG;Ter139=] | |
NM_002256.4:c.417_*1delinsAG MANE Select | NP_002247.3:n.[c.417_*1delinsAG;Ter139=] |