HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153737101_153737102delinsCA , CM000685.2:g.153737101_153737102delinsCA | GRCh38 |
NC_000023.10:g.153002555_153002556delinsCA , CM000685.1:g.153002555_153002556delinsCA | GRCh37 |
NC_000023.9:g.152655749_152655750delinsCA | NCBI36 |
NG_009022.2:g.17234_17235delinsCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000218104.6:c.1394-56_1394-55delinsCA MANE Select | ENSP00000218104.3:n.1394-56_1394-55delins... | |
ENST00000218104.5:c.1394-56_1394-55delinsCA | ENSP00000218104.3:n.1394-56_1394-55delins... | |
ENST00000443684.2:n.397-56_397-55delinsCA | ||
NM_000033.3:c.1394-56_1394-55delinsCA | NP_000024.2:n.1394-56_1394-55delinsCA | |
XR_938507.1:n.1866-56_1866-55delinsCA | ||
XR_938507.2:n.1866-56_1866-55delinsCA | ||
NM_000033.4:c.1394-56_1394-55delinsCA MANE Select | NP_000024.2:n.1394-56_1394-55delinsCA |