HGVS | Genome Assembly |
---|---|
NC_000002.12:g.176118880_176118881insAAAAA , CM000664.2:g.176118880_176118881insAAAAA | GRCh38 |
NC_000002.11:g.176983608_176983609insAAAAA , CM000664.1:g.176983608_176983609insAAAAA | GRCh37 |
NC_000002.10:g.176691854_176691855insAAAAA | NCBI36 |
NG_008133.2:g.12117_12118insAAAAA , LRG_246:g.12117_12118insAAAAA | |
NG_009225.1:g.1196_1197insAAAAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000249501.5:c.746-74_746-73insAAAAA MANE Select | ENSP00000249501.4:n.746-74_746-73insAAAAA | |
ENST00000249501.4:c.746-74_746-73insAAAAA | ENSP00000249501.4:n.746-74_746-73insAAAAA | |
ENST00000490088.2:n.570-74_570-73insAAAAA | ||
ENST00000549469.1:n.617-74_617-73insAAAAA | ||
NM_002148.3:c.746-74_746-73insAAAAA , LRG_246t1:c.746-74_746-73insAAAAA | NP_002139.2:n.746-74_746-73insAAAAA | |
NM_002148.4:c.746-74_746-73insAAAAA MANE Select | NP_002139.2:n.746-74_746-73insAAAAA |