HGVS | Genome Assembly |
---|---|
NC_000002.12:g.216205568_216205570delinsCAT , CM000664.2:g.216205568_216205570delinsCAT | GRCh38 |
NC_000002.11:g.217070291_217070293delinsCAT , CM000664.1:g.217070291_217070293delinsCAT | GRCh37 |
NC_000002.10:g.216778536_216778538delinsCAT | NCBI36 |
NG_029780.1:g.101272_101274delinsCAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000392132.7:c.*366_*368delinsCAT MANE Select | ENSP00000375977.2:n.*366_*368delinsCAT | |
ENST00000392132.6:c.*366_*368delinsCAT | ENSP00000375977.2:n.*366_*368delinsCAT | |
ENST00000392133.7:c.*366_*368delinsCAT | ENSP00000375978.3:n.*366_*368delinsCAT | |
NM_021141.3:c.*366_*368delinsCAT | NP_066964.1:n.*366_*368delinsCAT | |
NM_021141.4:c.*366_*368delinsCAT MANE Select | NP_066964.1:n.*366_*368delinsCAT |