HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659487del , CM000685.2:g.136659487del | GRCh38 |
NC_000023.10:g.135741646del , CM000685.1:g.135741646del | GRCh37 |
NC_000023.9:g.135569312del | NCBI36 |
NG_007280.1:g.16311del , LRG_141:g.16311del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*476del | ENSP00000512122.1:n.*476del | |
ENST00000695725.1:c.*413del | ENSP00000512123.1:n.*413del | |
ENST00000695726.1:n.2826del | ||
ENST00000695729.1:n.3661del | ||
ENST00000370629.7:c.*72del MANE Select | ENSP00000359663.2:n.*72del | |
ENST00000370628.2:c.*72del | ENSP00000359662.2:n.*72del | |
ENST00000370629.6:c.*72del | ENSP00000359663.2:n.*72del | |
NM_000074.2:c.*72del , LRG_141t1:c.*72del | NP_000065.1:n.*72del | |
NM_000074.3:c.*72del MANE Select | NP_000065.1:n.*72del |