HGVS | Genome Assembly |
---|---|
NC_000011.10:g.128891447_128891457dup , CM000673.2:g.128891447_128891457dup | GRCh38 |
NC_000011.9:g.128761342_128761352dup , CM000673.1:g.128761342_128761352dup | GRCh37 |
NC_000011.8:g.128266552_128266562dup | NCBI36 |
NG_023406.2:g.5030_5040dup , LRG_333:g.5030_5040dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000529694.6:c.-285_-275dup MANE Select | ENSP00000433295.1:n.-285_-275dup | |
ENST00000529694.5:c.-285_-275dup | ENSP00000433295.1:n.-285_-275dup | |
NM_000890.3:c.-285_-275dup , LRG_333t1:c.-285_-275dup | NP_000881.3:n.-285_-275dup | |
NM_000890.4:c.-285_-275dup | NP_000881.3:n.-285_-275dup | |
NM_001354169.1:c.-374_-364dup | NP_001341098.1:n.-374_-364dup | |
NM_000890.5:c.-285_-275dup MANE Select | NP_000881.3:n.-285_-275dup | |
NM_001354169.2:c.-374_-364dup | NP_001341098.1:n.-374_-364dup |