HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47003932_47003933insTACA , CM000681.2:g.47003932_47003933insTACA | GRCh38 |
NC_000019.9:g.47507189_47507190insTACA , CM000681.1:g.47507189_47507190insTACA | GRCh37 |
NC_000019.8:g.52199029_52199030insTACA | NCBI36 |
NG_047014.1:g.90366_90367insTACA | |
NG_047014.2:g.147936_147937insTACA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7744_7745insTACA | ENSP00000385720.2:n.7744_7745insTACA | |
ENST00000672722.1:c.*3244_*3245insTACA MANE Select | ENSP00000500409.1:n.*3244_*3245insTACA | |
ENST00000404338.7:c.7744_7745insTACA | ENSP00000385720.2:n.7744_7745insTACA | |
ENST00000614079.1:c.7321_7322insTACA | ENSP00000483730.1:n.7321_7322insTACA | |
NM_004491.4:c.7744_7745insTACA | NP_004482.4:n.7744_7745insTACA | |
NM_004491.5:c.*3244_*3245insTACA MANE Select | NP_004482.4:n.*3244_*3245insTACA |