HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133352912del , CM000671.2:g.133352912del | GRCh38 |
NC_000009.10:g.135209588del | NCBI36 |
NG_008477.1:g.8596del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371974.8:c.516-145del MANE Select | ENSP00000361042.3:n.516-145del | |
ENST00000371974.7:c.516-145del | ENSP00000361042.3:n.516-145del | |
ENST00000437995.1:n.462-181del | ||
ENST00000495952.5:n.506-145del | ||
ENST00000615505.4:c.189-145del | ENSP00000482067.1:n.189-145del | |
NM_001280787.1:c.189-145del | NP_001267716.1:n.189-145del | |
NM_003172.3:c.516-145del | NP_003163.1:n.516-145del | |
XM_011518942.1:c.189-145del | XP_011517244.1:n.189-145del | |
NM_003172.4:c.516-145del MANE Select | NP_003163.1:n.516-145del |