HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116832959del , CM000673.2:g.116832959del | GRCh38 |
NC_000011.9:g.116703675del , CM000673.1:g.116703675del | GRCh37 |
NC_000011.8:g.116208885del | NCBI36 |
NG_008949.1:g.8052del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000227667.8:c.*75del MANE Select | ENSP00000227667.2:n.*75del | |
ENST00000227667.7:c.*75del | ENSP00000227667.2:n.*75del | |
ENST00000375345.3:c.*75del | ENSP00000364494.1:n.*75del | |
ENST00000630701.1:c.429del | ENSP00000486182.1:n.429del | |
NM_000040.1:c.*75del | NP_000031.1:n.*75del | |
NM_000040.2:c.*75del | NP_000031.1:n.*75del | |
NM_000040.3:c.*75del MANE Select | NP_000031.1:n.*75del |