HGVS | Genome Assembly |
---|---|
NC_000004.12:g.71030698dup , CM000666.2:g.71030698dup | GRCh38 |
NC_000004.11:g.71896415dup , CM000666.1:g.71896415dup | GRCh37 |
NC_000004.10:g.72115279dup | NCBI36 |
NG_023303.1:g.42151dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286648.10:c.*1320dup MANE Select | ENSP00000286648.5:n.*1320dup | |
ENST00000286648.9:c.*1320dup | ENSP00000286648.5:n.*1320dup | |
ENST00000503359.5:c.*2047dup | ENSP00000426389.1:n.*2047dup | |
ENST00000504730.5:c.*1387dup | ENSP00000425578.1:n.*1387dup | |
ENST00000504952.1:c.*1246dup | ENSP00000421508.1:n.*1246dup | |
NM_000788.2:c.*1320dup | NP_000779.1:n.*1320dup | |
NM_000788.3:c.*1320dup MANE Select | NP_000779.1:n.*1320dup |