HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713759_6713760insT , CM000681.2:g.6713759_6713760insT | GRCh38 |
NC_000019.9:g.6713770_6713771insT , CM000681.1:g.6713770_6713771insT | GRCh37 |
NC_000019.8:g.6664770_6664771insT | NCBI36 |
NG_009557.1:g.11892_11893insA , LRG_27:g.11892_11893insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.650+232_650+233insA | ENSP00000512083.1:n.650+232_650+233insA | |
ENST00000245907.11:c.773+232_773+233insA MANE Select | ENSP00000245907.4:n.773+232_773+233insA | |
ENST00000245907.10:c.773+232_773+233insA | ENSP00000245907.4:n.773+232_773+233insA | |
ENST00000595577.1:n.277+232_277+233insA | ||
ENST00000597442.5:n.23+6_23+7insA | ||
NM_000064.3:c.773+232_773+233insA | NP_000055.2:n.773+232_773+233insA | |
NM_000064.4:c.773+232_773+233insA MANE Select | NP_000055.2:n.773+232_773+233insA |