HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47003930_47003931insTACA , CM000681.2:g.47003930_47003931insTACA | GRCh38 |
NC_000019.9:g.47507187_47507188insTACA , CM000681.1:g.47507187_47507188insTACA | GRCh37 |
NC_000019.8:g.52199027_52199028insTACA | NCBI36 |
NG_047014.1:g.90364_90365insTACA | |
NG_047014.2:g.147934_147935insTACA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7742_7743insTACA | ENSP00000385720.2:n.7742_7743insTACA | |
ENST00000672722.1:c.*3242_*3243insTACA MANE Select | ENSP00000500409.1:n.*3242_*3243insTACA | |
ENST00000404338.7:c.7742_7743insTACA | ENSP00000385720.2:n.7742_7743insTACA | |
ENST00000614079.1:c.7319_7320insTACA | ENSP00000483730.1:n.7319_7320insTACA | |
NM_004491.4:c.7742_7743insTACA | NP_004482.4:n.7742_7743insTACA | |
NM_004491.5:c.*3242_*3243insTACA MANE Select | NP_004482.4:n.*3242_*3243insTACA |