HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44377667del , CM000679.2:g.44377667del | GRCh38 |
NC_000017.10:g.42455035del , CM000679.1:g.42455035del | GRCh37 |
NC_000017.9:g.39810561del | NCBI36 |
NG_008331.1:g.16840del , LRG_479:g.16840del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262407.6:c.2187+32del MANE Select | ENSP00000262407.5:n.2187+32del | |
ENST00000648408.1:c.1618+32del | ||
ENST00000262407.5:c.2187+32del | ENSP00000262407.5:n.2187+32del | |
ENST00000592462.5:n.982+32del | ||
NM_000419.3:c.2187+32del , LRG_479t1:c.2187+32del | NP_000410.2:n.2187+32del | |
XM_011524749.1:c.2187+32del | XP_011523051.1:n.2187+32del | |
XM_011524750.1:c.2187+32del | XP_011523052.1:n.2187+32del | |
NM_000419.4:c.2187+32del | NP_000410.2:n.2187+32del | |
NM_000419.5:c.2187+32del MANE Select | NP_000410.2:n.2187+32del |