HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10645335_10645336insAAC , CM000682.2:g.10645335_10645336insAAC | GRCh38 |
NC_000020.10:g.10625983_10625984insAAC , CM000682.1:g.10625983_10625984insAAC | GRCh37 |
NC_000020.9:g.10573983_10573984insAAC | NCBI36 |
NG_007496.1:g.33712_33713insTTG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000254958.10:c.2113+21_2113+22insTTG MANE Select | ENSP00000254958.4:n.2113+21_2113+22insTTG... | |
ENST00000617965.2:n.2702+21_2702+22insTTG | ||
ENST00000254958.9:c.2113+21_2113+22insTTG | ENSP00000254958.4:n.2113+21_2113+22insTTG... | |
ENST00000423891.6:n.1979+21_1979+22insTTG | ||
ENST00000488480.2:n.510+21_510+22insTTG | ||
NM_000214.2:c.2113+21_2113+22insTTG | NP_000205.1:n.2113+21_2113+22insTTG | |
NM_000214.3:c.2113+21_2113+22insTTG MANE Select | NP_000205.1:n.2113+21_2113+22insTTG |