HGVS | Genome Assembly |
---|---|
NC_000016.10:g.1445138dup , CM000678.2:g.1445138dup | GRCh38 |
NC_000016.9:g.1495139dup , CM000678.1:g.1495139dup | GRCh37 |
NC_000016.8:g.1435140dup | NCBI36 |
NG_007567.1:g.34951dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382745.9:c.*1497dup MANE Select | ENSP00000372193.4:n.*1497dup | |
ENST00000382745.8:c.*1497dup | ENSP00000372193.4:n.*1497dup | |
ENST00000448525.5:c.*1497dup | ENSP00000410907.1:n.*1497dup | |
ENST00000563642.6:n.3984dup | ||
NM_001114331.2:c.*1497dup | NP_001107803.1:n.*1497dup | |
NM_001287.5:c.*1497dup | NP_001278.1:n.*1497dup | |
XM_011522354.1:c.*1497dup | XP_011520656.1:n.*1497dup | |
NM_001287.6:c.*1497dup MANE Select | NP_001278.1:n.*1497dup | |
NM_001114331.3:c.*1497dup | NP_001107803.1:n.*1497dup |