HGVS | Genome Assembly |
---|---|
NC_000002.12:g.201623514dup , CM000664.2:g.201623514dup | GRCh38 |
NC_000002.11:g.202488237dup , CM000664.1:g.202488237dup | GRCh37 |
NC_000002.10:g.202196482dup | NCBI36 |
NG_032049.1:g.25017dup | |
NG_051007.1:g.670dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000621467.5:c.*742dup | ENSP00000480508.2:n.*742dup | |
ENST00000686475.1:n.1909dup | ||
ENST00000409883.7:c.*742dup MANE Select | ENSP00000386264.2:n.*742dup | |
ENST00000409444.6:c.*742dup | ENSP00000387203.2:n.*742dup | |
ENST00000409883.6:c.*742dup | ENSP00000386264.2:n.*742dup | |
ENST00000495329.1:n.1108dup | ||
NM_001044385.2:c.*742dup | NP_001037850.1:n.*742dup | |
NM_152388.3:c.*742dup | NP_689601.2:n.*742dup | |
NM_001044385.3:c.*742dup MANE Select | NP_001037850.1:n.*742dup | |
NM_152388.4:c.*742dup | NP_689601.2:n.*742dup |