HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43887299_43887301delinsAAG , CM000664.2:g.43887299_43887301delinsAAG | GRCh38 |
NC_000002.11:g.44114438_44114440delinsAAG , CM000664.1:g.44114438_44114440delinsAAG | GRCh37 |
NC_000002.10:g.43967942_43967944delinsAAG | NCBI36 |
NG_008247.1:g.113705_113707delinsCTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2251_2253delinsCTT | ||
ENST00000684454.1:n.9348_9350delinsCTT | ||
ENST00000260665.12:c.*1299_*1301delinsCTT MANE Select | ENSP00000260665.7:n.*1299_*1301delinsCTT | |
ENST00000260665.11:c.*1299_*1301delinsCTT | ENSP00000260665.7:n.*1299_*1301delinsCTT | |
NM_133259.3:c.*1299_*1301delinsCTT | NP_573566.2:n.*1299_*1301delinsCTT | |
XR_002958896.1:n.5666_5668delinsCTT | ||
NM_133259.4:c.*1299_*1301delinsCTT MANE Select | NP_573566.2:n.*1299_*1301delinsCTT |