HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42903901dup , CM000679.2:g.42903901dup | GRCh38 |
NC_000017.10:g.41055918dup , CM000679.1:g.41055918dup | GRCh37 |
NC_000017.9:g.38309444dup | NCBI36 |
NG_011808.1:g.8104dup , LRG_147:g.8104dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253801.7:c.231-30dup MANE Select | ENSP00000253801.1:n.231-30dup | |
ENST00000253801.6:c.231-30dup | ENSP00000253801.1:n.231-30dup | |
ENST00000585489.1:c.231-30dup | ENSP00000466202.1:n.231-30dup | |
ENST00000588481.1:n.296-30dup | ||
ENST00000592383.5:c.231-30dup | ENSP00000465958.1:n.231-30dup | |
NM_000151.3:c.231-30dup | NP_000142.2:n.231-30dup | |
NM_001270397.1:c.231-30dup | NP_001257326.1:n.231-30dup | |
NM_000151.4:c.231-30dup MANE Select | NP_000142.2:n.231-30dup | |
NM_001270397.2:c.231-30dup | NP_001257326.1:n.231-30dup |