HGVS | Genome Assembly |
---|---|
NC_000005.10:g.173234640del , CM000667.2:g.173234640del | GRCh38 |
NC_000005.9:g.172661643del , CM000667.1:g.172661643del | GRCh37 |
NC_000005.8:g.172594249del | NCBI36 |
NG_013340.1:g.5674del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000329198.5:c.334+111del MANE Select | ENSP00000327758.4:n.334+111del | |
ENST00000329198.4:c.334+111del | ENSP00000327758.4:n.334+111del | |
ENST00000424406.2:c.334+111del | ENSP00000395378.2:n.334+111del | |
ENST00000517440.1:c.334+111del | ENSP00000429905.1:n.334+111del | |
ENST00000521848.1:c.334+111del | ENSP00000427906.1:n.334+111del | |
NM_001166175.1:c.334+111del | NP_001159647.1:n.334+111del | |
NM_001166176.1:c.334+111del | NP_001159648.1:n.334+111del | |
NM_004387.3:c.334+111del | NP_004378.1:n.334+111del | |
XM_017009071.2:c.334+111del | XP_016864560.1:n.334+111del | |
NM_004387.4:c.334+111del MANE Select | NP_004378.1:n.334+111del | |
NM_001166175.2:c.334+111del | NP_001159647.1:n.334+111del | |
NM_001166176.2:c.334+111del | NP_001159648.1:n.334+111del |