HGVS | Genome Assembly |
---|---|
NC_000001.11:g.109264395_109264396insCCCCCCAGCCG , CM000663.2:g.109264395_109264396insCCCCCCAGCCG | GRCh38 |
NC_000001.10:g.109807017_109807018insCCCCCCAGCCG , CM000663.1:g.109807017_109807018insCCCCCCAGCCG | GRCh37 |
NC_000001.9:g.109608540_109608541insCCCCCCAGCCG | NCBI36 |
NG_052669.1:g.19691_19692insCCCCCCAGCCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271332.4:c.5289+30_5289+31insCCCCCCAGCCG MANE Select | ENSP00000271332.3:n.5289+30_5289+31insCCCCCCAGCCG | |
ENST00000271332.3:c.5289+30_5289+31insCCCCCCAGCCG | ENSP00000271332.3:n.5289+30_5289+31insCCCCCCAGCCG | |
NM_001408.2:c.5289+30_5289+31insCCCCCCAGCCG | NP_001399.1:n.5289+30_5289+31insCCCCCCAGCCG | |
XM_005270580.3:c.5289+30_5289+31insCCCCCCAGCCG | XP_005270637.1:n.5289+30_5289+31insCCCCCCAGCCG | |
NM_001408.3:c.5289+30_5289+31insCCCCCCAGCCG MANE Select | NP_001399.1:n.5289+30_5289+31insCCCCCCAGCCG |