HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153736074_153736075insA , CM000685.2:g.153736074_153736075insA | GRCh38 |
NC_000023.10:g.153001528_153001529insA , CM000685.1:g.153001528_153001529insA | GRCh37 |
NC_000023.9:g.152654722_152654723insA | NCBI36 |
NG_009022.2:g.16207_16208insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1082-38_1082-37insA MANE Select | ENSP00000218104.3:n.1082-38_1082-37insA | |
ENST00000218104.5:c.1082-38_1082-37insA | ENSP00000218104.3:n.1082-38_1082-37insA | |
ENST00000443684.2:n.85-38_85-37insA | ||
NM_000033.3:c.1082-38_1082-37insA | NP_000024.2:n.1082-38_1082-37insA | |
XR_938507.1:n.1498-38_1498-37insA | ||
XR_938507.2:n.1498-38_1498-37insA | ||
NM_000033.4:c.1082-38_1082-37insA MANE Select | NP_000024.2:n.1082-38_1082-37insA |