HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94047186_94047187insA , CM000663.2:g.94047186_94047187insA | GRCh38 |
NC_000001.10:g.94512742_94512743insA , CM000663.1:g.94512742_94512743insA | GRCh37 |
NC_000001.9:g.94285330_94285331insA | NCBI36 |
NG_009073.1:g.78963_78964insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.2744-94_2744-93insT MANE Select | ENSP00000359245.3:n.2744-94_2744-93insT | |
ENST00000649773.1:c.2522-94_2522-93insT | ENSP00000496882.1:n.2522-94_2522-93insT | |
ENST00000370225.3:c.2744-94_2744-93insT | ENSP00000359245.3:n.2744-94_2744-93insT | |
ENST00000536513.5:c.-64-7098_-64-7097insT | ENSP00000439707.2:n.-64-7098_-64-7097insT | |
NM_000350.2:c.2744-94_2744-93insT | NP_000341.2:n.2744-94_2744-93insT | |
NM_000350.3:c.2744-94_2744-93insT MANE Select | NP_000341.2:n.2744-94_2744-93insT |