HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94047189_94047201dup , CM000663.2:g.94047189_94047201dup | GRCh38 |
NC_000001.10:g.94512745_94512757dup , CM000663.1:g.94512745_94512757dup | GRCh37 |
NC_000001.9:g.94285333_94285345dup | NCBI36 |
NG_009073.1:g.78951_78963dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.2744-106_2744-94dup MANE Select | ENSP00000359245.3:n.2744-106_2744-94dup | |
ENST00000649773.1:c.2522-106_2522-94dup | ENSP00000496882.1:n.2522-106_2522-94dup | |
ENST00000370225.3:c.2744-106_2744-94dup | ENSP00000359245.3:n.2744-106_2744-94dup | |
ENST00000536513.5:c.-64-7110_-64-7098dup | ENSP00000439707.2:n.-64-7110_-64-7098dup | |
NM_000350.2:c.2744-106_2744-94dup | NP_000341.2:n.2744-106_2744-94dup | |
NM_000350.3:c.2744-106_2744-94dup MANE Select | NP_000341.2:n.2744-106_2744-94dup |