HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10652674_10652675insAGAT , CM000682.2:g.10652674_10652675insAGAT | GRCh38 |
NC_000020.10:g.10633322_10633323insAGAT , CM000682.1:g.10633322_10633323insAGAT | GRCh37 |
NC_000020.9:g.10581322_10581323insAGAT | NCBI36 |
NG_007496.1:g.26372_26373insATCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.756-77_756-76insATCT MANE Select | ENSP00000254958.4:n.756-77_756-76insATCT | |
ENST00000617965.2:n.48_49insATCT | ||
ENST00000254958.9:c.756-77_756-76insATCT | ENSP00000254958.4:n.756-77_756-76insATCT | |
ENST00000423891.6:n.622-77_622-76insATCT | ||
ENST00000617965.1:n.48_49insATCT | ||
NM_000214.2:c.756-77_756-76insATCT | NP_000205.1:n.756-77_756-76insATCT | |
NM_000214.3:c.756-77_756-76insATCT MANE Select | NP_000205.1:n.756-77_756-76insATCT |