HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94021466_94021467insAGA , CM000663.2:g.94021466_94021467insAGA | GRCh38 |
NC_000001.10:g.94487022_94487023insAGA , CM000663.1:g.94487022_94487023insAGA | GRCh37 |
NC_000001.9:g.94259610_94259611insAGA | NCBI36 |
NG_009073.1:g.104683_104684insTCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4849-58_4849-57insTCT MANE Select | ENSP00000359245.3:n.4849-58_4849-57insTCT | |
ENST00000370225.3:c.4849-58_4849-57insTCT | ENSP00000359245.3:n.4849-58_4849-57insTCT | |
ENST00000460514.1:n.343-58_343-57insTCT | ||
ENST00000536513.5:c.1225-58_1225-57insTCT | ENSP00000439707.2:n.1225-58_1225-57insTCT | |
NM_000350.2:c.4849-58_4849-57insTCT | NP_000341.2:n.4849-58_4849-57insTCT | |
NM_000350.3:c.4849-58_4849-57insTCT MANE Select | NP_000341.2:n.4849-58_4849-57insTCT |