HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43887166_43887171delinsATGCTT , CM000664.2:g.43887166_43887171delinsATGCTT | GRCh38 |
NC_000002.11:g.44114305_44114310delinsATGCTT , CM000664.1:g.44114305_44114310delinsATGCTT | GRCh37 |
NC_000002.10:g.43967809_43967814delinsATGCTT | NCBI36 |
NG_008247.1:g.113835_113840delinsAAGCAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000682612.1:c.2381_2386delinsAAGCAT | ||
ENST00000684454.1:n.9478_9483delinsAAGCAT | ||
ENST00000260665.12:c.*1429_*1434delinsAAGCAT MANE Select | ENSP00000260665.7:n.*1429_*1434delinsAAGCAT | |
ENST00000260665.11:c.*1429_*1434delinsAAGCAT | ENSP00000260665.7:n.*1429_*1434delinsAAGCAT | |
NM_133259.3:c.*1429_*1434delinsAAGCAT | NP_573566.2:n.*1429_*1434delinsAAGCAT | |
XR_002958896.1:n.5796_5801delinsAAGCAT | ||
NM_133259.4:c.*1429_*1434delinsAAGCAT MANE Select | NP_573566.2:n.*1429_*1434delinsAAGCAT |