HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4898680dup , CM000679.2:g.4898680dup | GRCh38 |
NC_000017.10:g.4801975dup , CM000679.1:g.4801975dup | GRCh37 |
NC_000017.9:g.4742754dup | NCBI36 |
NG_008029.2:g.9396dup | |
NG_028005.1:g.70341dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000649488.2:c.*56dup MANE Select | ENSP00000497829.1:n.*56dup | |
ENST00000649830.1:c.*174dup | ENSP00000496907.1:n.*174dup | |
ENST00000652550.1:n.1264dup | ||
ENST00000293780.4:c.*56dup | ENSP00000293780.4:n.*56dup | |
ENST00000572438.1:n.1224dup | ||
NM_000080.3:c.*56dup | NP_000071.1:n.*56dup | |
NM_000080.4:c.*56dup MANE Select | NP_000071.1:n.*56dup | |
XM_017024115.1:c.*56dup | XP_016879604.1:n.*56dup |