HGVS | Genome Assembly |
---|---|
NC_000004.12:g.71030652dup , CM000666.2:g.71030652dup | GRCh38 |
NC_000004.11:g.71896369dup , CM000666.1:g.71896369dup | GRCh37 |
NC_000004.10:g.72115233dup | NCBI36 |
NG_023303.1:g.42105dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286648.10:c.*1274dup MANE Select | ENSP00000286648.5:n.*1274dup | |
ENST00000286648.9:c.*1274dup | ENSP00000286648.5:n.*1274dup | |
ENST00000503359.5:c.*2001dup | ENSP00000426389.1:n.*2001dup | |
ENST00000504730.5:c.*1341dup | ENSP00000425578.1:n.*1341dup | |
ENST00000504952.1:c.*1200dup | ENSP00000421508.1:n.*1200dup | |
NM_000788.2:c.*1274dup | NP_000779.1:n.*1274dup | |
NM_000788.3:c.*1274dup MANE Select | NP_000779.1:n.*1274dup |