HGVS | Genome Assembly |
---|---|
NC_000010.11:g.86124270del , CM000672.2:g.86124270del | GRCh38 |
NC_000010.10:g.87884027del , CM000672.1:g.87884027del | GRCh37 |
NC_000010.9:g.87874007del | NCBI36 |
NG_011875.1:g.247225del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000327946.12:c.726+14550del MANE Select | ENSP00000330148.7:n.726+14550del | |
ENST00000327946.11:c.726+14550del | ENSP00000330148.7:n.726+14550del | |
ENST00000464741.2:c.726+14550del | ENSP00000433064.1:n.726+14550del | |
NM_017551.2:c.726+14550del | NP_060021.1:n.726+14550del | |
XM_011539720.1:c.726+14550del | XP_011538022.1:n.726+14550del | |
XM_011539720.2:c.726+14550del | XP_011538022.1:n.726+14550del | |
NM_017551.3:c.726+14550del MANE Select | NP_060021.1:n.726+14550del |