HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19957588_19957591delinsTCAC , CM000670.2:g.19957588_19957591delinsTCAC | GRCh38 |
NC_000008.10:g.19815099_19815102delinsTCAC , CM000670.1:g.19815099_19815102delinsTCAC | GRCh37 |
NC_000008.9:g.19859379_19859382delinsTCAC | NCBI36 |
NG_008855.1:g.23518_23521delinsTCAC | |
NG_008855.2:g.60872_60875delinsTCAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.1018+1505_1018+1508delinsTCAC MANE Select | ENSP00000497642.1:n.1018+1505_1018+1508de... | |
ENST00000650478.1:c.79+1505_79+1508delinsTCAC | ENSP00000497560.1:n.79+1505_79+1508delins... | |
ENST00000311322.8:c.1018+1505_1018+1508delinsTCAC | ENSP00000309757.6:n.1018+1505_1018+1508de... | |
NM_000237.2:c.1018+1505_1018+1508delinsTCAC | NP_000228.1:n.1018+1505_1018+1508delinsTC... | |
NM_000237.3:c.1018+1505_1018+1508delinsTCAC MANE Select | NP_000228.1:n.1018+1505_1018+1508delinsTC... |