HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67585232del , CM000673.2:g.67585232del | GRCh38 |
NC_000011.9:g.67352703del , CM000673.1:g.67352703del | GRCh37 |
NC_000011.8:g.67109279del | NCBI36 |
NG_012075.1:g.6638del , LRG_723:g.6638del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000398603.6:c.327del | ENSP00000381604.1:p.Tyr109Ter | |
ENST00000398606.10:c.327del MANE Select | ENSP00000381607.3:p.Tyr109Ter | |
ENST00000646888.1:c.*43del | ENSP00000494477.1:n.*43del | |
ENST00000398603.5:c.327del | ENSP00000381604.1:p.Tyr109Ter | |
ENST00000398606.7:c.327del | ENSP00000381607.3:p.Tyr109Ter | |
ENST00000467591.1:n.438del | ||
ENST00000494593.1:n.1122del | ||
ENST00000498765.5:c.390del | ||
NM_000852.3:c.327del , LRG_723t1:c.327del | NP_000843.1:p.Tyr109Ter | |
NM_000852.4:c.327del MANE Select | NP_000843.1:p.Tyr109Ter |